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FC-140-1003 Illumina Nextera Rapid Capture Exome
具體成交價(jià)以合同協(xié)議為準(zhǔn)
- 公司名稱 上海易匯生物科技有限公司
- 品牌 其他品牌
- 型號(hào) FC-140-1003
- 產(chǎn)地 美國(guó)進(jìn)口
- 廠商性質(zhì) 生產(chǎn)廠家
- 更新時(shí)間 2020/2/17 9:39:22
- 訪問次數(shù) 1764
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| 供貨周期 | 現(xiàn)貨 | 規(guī)格 | 盒 |
|---|---|---|---|
| 貨號(hào) | FC-140-1003 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,環(huán)保,食品,化工,生物產(chǎn)業(yè) |
| 主要用途 | 基因測(cè)序 |
Illumina Nextera Rapid Capture Exome
Illumina Nextera Rapid Capture Exome
美國(guó)Illumina公司是的新一代生命科學(xué)工具的開發(fā)和生產(chǎn)者，并開發(fā)大規(guī)模分析遺傳變異和生物功能的集成工具。我們利用技術(shù)，為測(cè)序、基因分型和基因表達(dá)提供全面的產(chǎn)品和服務(wù)，還將進(jìn)入分子診斷市場(chǎng)。我們的客戶包含**的基因研究中心、藥廠、研究院、臨床研究機(jī)構(gòu)和生物公司。我們的工具有足夠的表現(xiàn)力、通量、成本效益和靈活性，使*的研究者能通過(guò)遺傳實(shí)驗(yàn)來(lái)得到有價(jià)值的信息。我們相信這個(gè)信息能使研究者把遺傳變異與生物功能關(guān)聯(lián)起來(lái)，從而加大藥物開發(fā)和臨床研究，讓疾病能更早地檢測(cè)出來(lái)，為患者提供更好的藥物。Illumina的目標(biāo)是用創(chuàng)新的技術(shù)以及革命性的檢測(cè)手段提供基因變異 和功能研究， 這些研究使得個(gè)人化醫(yī)療成為可能。作為一家性公司，Illumina 以嶄新的技術(shù) 在創(chuàng)新性，靈活性，可升級(jí)性，以及**的服務(wù)與支持等方面創(chuàng)新了新的業(yè)界標(biāo)準(zhǔn)。illumina于1998年4月創(chuàng)立，2000年7月于Nasdaq上市，總部設(shè)在加利福尼亞的圣迭戈。我們利用技術(shù)，為測(cè)序、基因分型和基因表達(dá)提供全面的產(chǎn)品和服務(wù)，還將進(jìn)入分子診斷市場(chǎng)。我們的客戶包含**的基因研究中心、藥廠、研究院、臨床研究機(jī)構(gòu)和生物公司。我們的工具有足夠的表現(xiàn)力、通量、成本效益和靈活性，使*的研究者能通過(guò)遺傳實(shí)驗(yàn)來(lái)得到有價(jià)值的信息。我們相信這個(gè)信息能使研究者把遺傳變異與生物功能關(guān)聯(lián)起來(lái)，從而加大藥物開發(fā)和臨床研究，讓疾病能更早的檢測(cè)出來(lái)，為患者提供更好的藥物。
上海易匯生物科技有限公司，是一家集研發(fā)、銷售為一體的生物企業(yè)，公司專注于生命科學(xué)和生物技術(shù)領(lǐng)域，專業(yè)提供分子生物學(xué)、免疫學(xué)、生命科學(xué)基礎(chǔ)研究以及臨床檢測(cè)等諸多領(lǐng)域的試劑、耗材、儀器等各類產(chǎn)品及生物技術(shù)服務(wù)。公司目前已銷售銷售 LKT Laboratories，Epigentek,Biovision，Abnova等歐美*，另與阿拉丁，麥克林，TCI等化學(xué)試劑生產(chǎn)商建立了長(zhǎng)期合作關(guān)系，公司與中科院上海生命科學(xué)研究院、上海交通大學(xué)、復(fù)旦大學(xué)和一大批生物醫(yī)藥技術(shù)公司建立了長(zhǎng)期合作，在綜合實(shí)力基礎(chǔ)上，整合資源效率，打造產(chǎn)學(xué)研一體化的創(chuàng)新平臺(tái)。公司成立以來(lái)與一大批醫(yī)藥集團(tuán)建立了長(zhǎng)期穩(wěn)定的合作，價(jià)格優(yōu)勢(shì)、信譽(yù)良好?？蛻舭ㄇ迦A、北大、中科院、上海交通、復(fù)旦、國(guó)藥等等。產(chǎn)品涵蓋了試劑、耗材、小型儀器、原材料等各種實(shí)驗(yàn)室使用的材料。
上海易匯生物科技有限公司擁有強(qiáng)大的采購(gòu)系統(tǒng)。只要您想得到。沒有公司采購(gòu)辦不到的。
上海易匯生物科技有限公司擁有完善的售后平臺(tái)。只要有售后。我們時(shí)間為您解決。
上海易匯生物科技有限公司直接與廠家合作。保證貨源正品。購(gòu)買無(wú)后顧之憂。
上海易匯生物科技有限公司不保證100%。但保證100%產(chǎn)品都是正品。
產(chǎn)品特點(diǎn)上海易匯生物科技有限公司，是一家集研發(fā)、銷售為一體的企業(yè)，公司專注于生命科學(xué)和生物技術(shù)領(lǐng)域，專業(yè)提供分子生物學(xué)、免疫學(xué)、生命科學(xué)基礎(chǔ)研究以及臨床檢測(cè)等諸多領(lǐng)域的試劑、耗材、儀器等各類產(chǎn)品及生物技術(shù)服務(wù)。公司目前已銷售銷售 LKT Laboratories，Epigentek,Biovision，Abnova 銷售Illumina Immunoway abcam SBA Takara等歐美*，另與阿拉丁，麥克林，TCI等化學(xué)試劑生產(chǎn)商建立了長(zhǎng)期合作關(guān)系，公司與中科院上海生命科學(xué)研究院、上海交通大學(xué)、復(fù)旦大學(xué)和一大批生物醫(yī)藥技術(shù)公司建立了長(zhǎng)期合作，在綜合實(shí)力基礎(chǔ)上，整合資源效率，打造產(chǎn)學(xué)研一體化的創(chuàng)新平臺(tái)。
合作單位公司成立以來(lái)與一大批醫(yī)藥集團(tuán)建立了長(zhǎng)期穩(wěn)定的合作，價(jià)格優(yōu)勢(shì)、信譽(yù)良好?？蛻舭ㄇ迦A、北大、中科院、上海交通、復(fù)旦、國(guó)藥等等。產(chǎn)品涵蓋了試劑、耗材、小型儀器、原材料等各種實(shí)驗(yàn)室使用的材料。
| Illumina/TruSeq DNA Methylation Kit (12 reactions)/EGMK81312/1 Ea | EGMK81312 | Illumina | 產(chǎn)品編號(hào)： EGMK81312美 元 價(jià)： $1009.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: Unlock small samples (50–100 ng DNA input) CpG, CHH, & CHG regions included for comprehensive, whole-genome results Fast protocol – five-hour method Capture full sample diversity Sequence the entire sample–no loss of information The process of bisulfite treatment denatures genomic DNA into single stranded DNA. TruSeq DNA Methylation converts single stranded DNA into an Illumina sequencing library. All ssDNA fragments are captured into an Illumina sequencing library, therefore eliminating the loss of diversity associated with other methods. Supported analysis in the cloud TruSeq DNA Methylation libraries can be aligned to the human genome and compared for differential methylation with Illumina BaseSpace Apps MethylSeq and MethylKit. These applications are fully supported and were developed specifically for TruSeq DNA Methylation library preparation. Example data sets for TruSeq DNA Methylation libraries, also available in BaseSpace Sequence Hub Data Central (use the “Methyl Seq” category filter), demonstrate unparalleled quality and seamless analysis. Deep coverage of critical genomic regions Depth of coverage is enhanced in genomic areas with BIOLOGical utility. TruSeq DNA Methylation captures full sample diversity of critical areas, including: Coding region start and end for exons from the canonical transcript of protein coding genes for genes known to be involved in cancer, taken from SOMA and CRUK panels (as well as literature-derived cancer genes) Genes defined by the American College of Medical Genetics as being medically relevant (ACMG genes) Exonic coding regions from Ensemble 70 List of 100 promoters defined by the Broad Institute as being of high interest and difficult to sequence | 1009 |
| Illumina/TruSeq Small RNA Set C MiniSeq Kit (1 library prep and 2 MiniSeq reagents)/20005615/1 Ea | 20005615 | Illumina | 產(chǎn)品編號(hào)： 20005615美 元 價(jià)： $3200.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Small RNA Library Preparation Kits provide reagents to generate small RNA libraries directly from total RNA. MicroRNAs (miRNAs) generated by Dicer processing are efficiently targeted by the included modified adapters. These kits enable multiplexed sequencing with the introduction of 48 unique indexes, allowing miRNA and small RNA discovery and profiling throughput to match the unparalleled output of Illumina sequencing. Indexes are added in a universal amplification reaction, greatly reducing ligation bias and ensuring accurate measurement of miRNA expression. Workflow improvements enable streamlined sample preparation, allowing economical studies covering all small RNA transcripts in any species. CompatIBLe applications include finding novel miRNAs, characterizing variation such as isomers with single-base resolution, and analyzing differential expression without prior assumptions. TruSeq Small RNA Sample Datasets The Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples were prepared using the TruSeq Small RNA Library Prep Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 36 bp read length configuration. The total yield was 0.91 Gb with 97% of bases at or above Q30. Browse the Data In BaseSpace Sequence Hub: View Run (primary analysis and metrics) View Project (secondary analysis with BaseSpace Apps) | 3,200.00 |
| Illumina/MiSeq FGx Reagent Kit/TG-143-1001/1 Ea | TG-143-1001 | Illumina | 產(chǎn)品編號(hào)： TG-143-1001美 元 價(jià)： $1400.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.簇生成和測(cè)序試劑公司分類： Cluster Generation & Sequencing Reagents | Product Highlights: This sequencing kit for forensic genomics applications is based on the MiSeq Reagent Kit v3, which enables the highest output of all MiSeq kits. This kit allows forensic genomics laboratories to: Simultaneously analyze a dense set of forensically relevant Markers at low, medium, or high sample throughput Extend read lengths Increase the number of reads to unlock new applications The MiSeq FGx Reagent Kit uses pre-filled, ready-to-use reagent cartridges, and offers the improved v3 chemistry to increase cluster density and read length as well as improve quality. MiSeq FGx Reagent Kit components are RFID-encoded and interact intelligently with the MiSeq FGx System to validate compatibility with forensic genomic applications. Specifications: Maximum Output 15 Gb Maximum Reads per Run 14 million Reagent Type Paired-End Sequencing,Cluster Generation,Sequencing by Synthesis Technology Sequencing System Compatibility MiSeq FGx | 1,400.00 |
| Illumina/TruSeq Targeted RNA Index Kit D (96 indexes, 384 samples)/RT-402-1004/1 Ea | RT-402-1004 | Illumina | 產(chǎn)品編號(hào)： RT-402-1004美 元 價(jià)： $1019.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Targeted RNA Expression Kits enable highly customizable mid- to high-plex gene expression profiling studies. You can define panels of 12-1,000 assays to target individual exons, isoforms, splice junctions, coding SNPS (cSNPs), gene fusions, and non-coding RNA transcripts, plus multiplex up to 384 samples. Generate the data equivalent of up to 25,000 individual RT-PCR assays in a single run.* Assays include convenient online panel design and ordering, a rapid and simple workflow starting with as little as 50 ng of RNA, and automated, on-instrument data analysis. Types of Study Designs Custom panels—select up to 1000 targets from a database of over 400,000 predesigned assays. Add-on (supplemental) content—add a second oligo pool of up to 1000 targets to a previously designed TruSeq Targeted RNA Expression custom panel. Start a Custom Project Order custom panels using DesignStudio, a free, user-friendly, web-based tool. Simply select the assays you need and add them to your order, with no design time. Log in to DesignStudio Browse TruSeq Targeted RNA Sample Data Human Brain Reference RNA (HBRR), Universal Human Reference RNA (UHRR), and human liver RNA samples were prepared using the TruSeq Targeted RNA Expression Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 51 bp read length configuration. The total yield was 2.04 Gb with 96.5% of bases at or above Q30. Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub View TruSeq Targeted RNA Project Data (secondary analysis with BaseSpace Apps) *Refers to instruments with catalog number SY-410-1001 and upgrade, or catalog number SY-410-1003 Specifications: Assay Time 1 day Hands-On Time 4 hours Input Quantity 50 ng RNA,50 ng high-quality total RNA,≥ 200 ng FFPE total RNA; Recommended quantity may vary with expression level, target plexity, and sample quality Content Specifications Choose from 400,000+ pre-designed targeted RNA-Seq assays. Or add content to a fixed panel or previously designed custom panel. Multiplexing Up to 384 samples per sequencing run Mechanism of Action Amplification Method Targeted RNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Transcript Variants Specialized Sample Types FFPE | 1,019.00 |
| Illumina/TruSeq Small RNA Set B MiniSeq Kit (1 library prep and 2 MiniSeq reagents)/20005614/1 Ea | 20005614 | Illumina | 產(chǎn)品編號(hào)： 20005614美 元 價(jià)： $3200.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Small RNA Library Preparation Kits provide reagents to generate small RNA libraries directly from total RNA. MicroRNAs (miRNAs) generated by Dicer processing are efficiently targeted by the included modified adapters. These kits enable multiplexed sequencing with the introduction of 48 unique indexes, allowing miRNA and small RNA discovery and profiling throughput to match the unparalleled output of Illumina sequencing. Indexes are added in a universal amplification reaction, greatly reducing ligation bias and ensuring accurate measurement of miRNA expression. Workflow improvements enable streamlined sample preparation, allowing economical studies covering all small RNA transcripts in any species. CompatIBLe applications include finding novel miRNAs, characterizing variation such as isomers with single-base resolution, and analyzing differential expression without prior assumptions. TruSeq Small RNA Sample Datasets The Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples were prepared using the TruSeq Small RNA Library Prep Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 36 bp read length configuration. The total yield was 0.91 Gb with 97% of bases at or above Q30. Browse the Data In BaseSpace Sequence Hub: View Run (primary analysis and metrics) View Project (secondary analysis with BaseSpace Apps) Specifications: Assay Time ~10.5 hours Hands-On Time ~30 minutes Input Quantity 25 to 100 ng total RNA from species with polyA tails Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails Multiplexing Up to 24-plex pooling with additional NeoPrep runs Sample Throughput Up to 16 samples per NeoPrep library card Species Category Drosophila,Any Species,Mouse,Zebrafish,Human,Rat,Plant,Nematode System Compatibility MiSeq,NextSeq 550,MiniSeq,NextSeq 500 Specialized Sample Types FFPE,Low Input Technology Sequencing Automation CapABIlity Liquid Handling Robots Variant Class Novel Transcripts,Transcript Variants Method miRNA and Small RNA Sequencing | 3,200.00 |
| Illumina/TruSeq Small RNA Library Prep Kit -Set B (24 rxns) (Set B: indexes 13-24)/RS-200-0024/1 Ea | RS-200-0024 | Illumina | 產(chǎn)品編號(hào)： RS-200-0024美 元 價(jià)： $2450.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Small RNA Library Preparation Kits provide reagents to generate small RNA libraries directly from total RNA. MicroRNAs (miRNAs) generated by Dicer processing are efficiently targeted by the included modified adapters. These kits enable multiplexed sequencing with the introduction of 48 unique indexes, allowing miRNA and small RNA discovery and profiling throughput to match the unparalleled output of Illumina sequencing. Indexes are added in a universal amplification reaction, greatly reducing ligation bias and ensuring accurate measurement of miRNA expression. Workflow improvements enable streamlined sample preparation, allowing economical studies covering all small RNA transcripts in any species. CompatIBLe applications include finding novel miRNAs, characterizing variation such as isomers with single-base resolution, and analyzing differential expression without prior assumptions. TruSeq Small RNA Sample Datasets The Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples were prepared using the TruSeq Small RNA Library Prep Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 36 bp read length configuration. The total yield was 0.91 Gb with 97% of bases at or above Q30. Browse the Data In BaseSpace Sequence Hub: View Run (primary analysis and metrics) View Project (secondary analysis with BaseSpace Apps) Specifications: Assay Time ~10.5 hours Hands-On Time ~30 minutes Input Quantity 25 to 100 ng total RNA from species with polyA tails Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails Multiplexing Up to 24-plex pooling with additional NeoPrep runs Sample Throughput Up to 16 samples per NeoPrep library card Species Category Drosophila,Any Species,Mouse,Zebrafish,Human,Rat,Plant,Nematode System Compatibility MiSeq,NextSeq 550,MiniSeq,NextSeq 500 Specialized Sample Types FFPE,Low Input Technology Sequencing Automation CapABIlity Liquid Handling Robots Variant Class Novel Transcripts,Transcript Variants Method miRNA and Small RNA Sequencing | 2,450.00 |
| Illumina/TruSeq Stranded mRNA Library Prep Kit for NeoPrep (16 samples, 24 indexes)/NP-202-1001/1 Ea | NP-202-1001 | Illumina | 產(chǎn)品編號(hào)： NP-202-1001美 元 價(jià)： $880.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: The TruSeq Stranded mRNA Library Prep Kit for NeoPrep offers a streamlined, cost-efficient, and scalable solution for coding transcriptome analysis. It enables robust interrogation of both standard and low-quality samples. Simplified and seamless workflow solution – Generate libraries with minimal hands-on time Unparalleled performance and reproducibility – Interrogate gene expression with TruSeq Stranded mRNA coverage and quality, and reduced user variABIlity Low input requirement – Begin library prep with as little as 25 ng total RNA Precise and Accurate Get precise measurement of mRNA strand orientation for detection of antisense transcription, enhanced transcript annotation, and increased alignment efficiency. High coverage uniformity enhances the discovery of features such as alternative transcripts, gene fusions, and allele-specific expression. Cost-Efficient Stranded information identifies from which of the 2 DNA strands a given RNA transcript was derived. This information provides increased confidence in transcript annotation, particularly for nonhuman samples. Identifying strand origin increases the percentage of reads that align, reducing sequencing costs per sample. NeoPrep System enhances TruSeq Stranded mRNA performance The NeoPrep System enhances TruSeq Stranded mRNA performance by providing high-quality reproducIBLe results, even with low input amounts of RNA. Digital microfluidics technology precisely manipulates droplets that perform the library prep workflow, within the tightly controlled environment of the NeoPrep library card. A simple, intuitive workflow delivers 16 libraries, eliminating most manual steps, and reducing hands-on time from ~4.5 hours to just 30 minutes. In addition, digital microfluidics requires less RNA input, enabling excellent performance from as little as 25 ng of total RNA. Specifications: Assay Time ~10.5 hours Hands-On Time ~30 minutes Input Quantity 25 to 100 ng total RNA from species with polyA tails Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails Multiplexing Up to 24-plex pooling with additional NeoPrep runs Sample Throughput Up to 16 samples per NeoPrep library card System Compatibility Genome Analyzer IIx,HiSeq 2000,MiSeq,NextSeq 550,HiSeq 3000,HiSeq 1000,NeoPrep,HiSeq 1500,NextSeq 500,HiSeq 2500,HiSeq 4000 Species Category Other,Mammalian,Bovine,Mouse,Human,Rat Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Novel Transcripts,Transcript Variants Technology Sequencing Method mRNA Sequencing Automation CapABIlity NeoPrep Digital Microfluidics | 880.00 |
| Illumina/TruSeq Targeted RNA Index Kit A (96 indexes, 384 samples)/RT-402-1001/1 Ea | RT-402-1001 | Illumina | 產(chǎn)品編號(hào)： RT-402-1001美 元 價(jià)： $1019.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Targeted RNA Expression Kits enable highly customizable mid- to high-plex gene expression profiling studies. You can define panels of 12-1,000 assays to target individual exons, isoforms, splice junctions, coding SNPS (cSNPs), gene fusions, and non-coding RNA transcripts, plus multiplex up to 384 samples. Generate the data equivalent of up to 25,000 individual RT-PCR assays in a single run.* Assays include convenient online panel design and ordering, a rapid and simple workflow starting with as little as 50 ng of RNA, and automated, on-instrument data analysis. Types of Study Designs Custom panels—select up to 1000 targets from a database of over 400,000 predesigned assays. Add-on (supplemental) content—add a second oligo pool of up to 1000 targets to a previously designed TruSeq Targeted RNA Expression custom panel. Start a Custom Project Order custom panels using DesignStudio, a free, user-friendly, web-based tool. Simply select the assays you need and add them to your order, with no design time. Log in to DesignStudio Browse TruSeq Targeted RNA Sample Data Human Brain Reference RNA (HBRR), Universal Human Reference RNA (UHRR), and human liver RNA samples were prepared using the TruSeq Targeted RNA Expression Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 51 bp read length configuration. The total yield was 2.04 Gb with 96.5% of bases at or above Q30. Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub View TruSeq Targeted RNA Project Data (secondary analysis with BaseSpace Apps) *Refers to instruments with catalog number SY-410-1001 and upgrade, or catalog number SY-410-1003 Specifications: Assay Time 1 day Hands-On Time 4 hours Input Quantity 50 ng RNA,50 ng high-quality total RNA,≥ 200 ng FFPE total RNA; Recommended quantity may vary with expression level, target plexity, and sample quality Content Specifications Choose from 400,000+ pre-designed targeted RNA-Seq assays. Or add content to a fixed panel or previously designed custom panel. Multiplexing Up to 384 samples per sequencing run Mechanism of Action Amplification Method Targeted RNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Transcript Variants Specialized Sample Types FFPE | 1,019.00 |
| Illumina/TruSeq Small RNA Library Prep Kit -Set C (24 rxns) (Set C: indexes 25-36)/RS-200-0036/1 Ea | RS-200-0036 | Illumina | 產(chǎn)品編號(hào)： RS-200-0036美 元 價(jià)： $2450.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Small RNA Library Preparation Kits provide reagents to generate small RNA libraries directly from total RNA. MicroRNAs (miRNAs) generated by Dicer processing are efficiently targeted by the included modified adapters. These kits enable multiplexed sequencing with the introduction of 48 unique indexes, allowing miRNA and small RNA discovery and profiling throughput to match the unparalleled output of Illumina sequencing. Indexes are added in a universal amplification reaction, greatly reducing ligation bias and ensuring accurate measurement of miRNA expression. Workflow improvements enable streamlined sample preparation, allowing economical studies covering all small RNA transcripts in any species. CompatIBLe applications include finding novel miRNAs, characterizing variation such as isomers with single-base resolution, and analyzing differential expression without prior assumptions. TruSeq Small RNA Sample Datasets The Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples were prepared using the TruSeq Small RNA Library Prep Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 36 bp read length configuration. The total yield was 0.91 Gb with 97% of bases at or above Q30. Browse the Data In BaseSpace Sequence Hub: View Run (primary analysis and metrics) View Project (secondary analysis with BaseSpace Apps) Specifications: Assay Time ~10.5 hours Hands-On Time ~30 minutes Input Quantity 25 to 100 ng total RNA from species with polyA tails Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails Multiplexing Up to 24-plex pooling with additional NeoPrep runs Sample Throughput Up to 16 samples per NeoPrep library card Species Category Drosophila,Any Species,Mouse,Zebrafish,Human,Rat,Plant,Nematode System Compatibility MiSeq,NextSeq 550,MiniSeq,NextSeq 500 Specialized Sample Types FFPE,Low Input Technology Sequencing Automation CapABIlity Liquid Handling Robots Variant Class Novel Transcripts,Transcript Variants Method miRNA and Small RNA Sequencing | 2,450.00 |
| Illumina/TruSeq Small RNA Library Prep Kit -Set A (24 rxns) (Set A: indexes 1-12)/RS-200-0012/1 Ea | RS-200-0012 | Illumina | 產(chǎn)品編號(hào)： RS-200-0012美 元 價(jià)： $2450.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Small RNA Library Preparation Kits provide reagents to generate small RNA libraries directly from total RNA. MicroRNAs (miRNAs) generated by Dicer processing are efficiently targeted by the included modified adapters. These kits enable multiplexed sequencing with the introduction of 48 unique indexes, allowing miRNA and small RNA discovery and profiling throughput to match the unparalleled output of Illumina sequencing. Indexes are added in a universal amplification reaction, greatly reducing ligation bias and ensuring accurate measurement of miRNA expression. Workflow improvements enable streamlined sample preparation, allowing economical studies covering all small RNA transcripts in any species. CompatIBLe applications include finding novel miRNAs, characterizing variation such as isomers with single-base resolution, and analyzing differential expression without prior assumptions. TruSeq Small RNA Sample Datasets The Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples were prepared using the TruSeq Small RNA Library Prep Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 36 bp read length configuration. The total yield was 0.91 Gb with 97% of bases at or above Q30. Browse the Data In BaseSpace Sequence Hub: View Run (primary analysis and metrics) View Project (secondary analysis with BaseSpace Apps) Specifications: Assay Time ~10.5 hours Hands-On Time ~30 minutes Input Quantity 25 to 100 ng total RNA from species with polyA tails Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails Multiplexing Up to 24-plex pooling with additional NeoPrep runs Sample Throughput Up to 16 samples per NeoPrep library card Species Category Drosophila,Any Species,Mouse,Zebrafish,Human,Rat,Plant,Nematode System Compatibility MiSeq,NextSeq 550,MiniSeq,NextSeq 500 Specialized Sample Types FFPE,Low Input Technology Sequencing Automation CapABIlity Liquid Handling Robots Variant Class Novel Transcripts,Transcript Variants Method miRNA and Small RNA Sequencing | 2,450.00 |
| Illumina/TruSeq Targeted RNA Index Kit C (96 indexes, 384 samples)/RT-402-1003/1 Ea | RT-402-1003 | Illumina | 產(chǎn)品編號(hào)： RT-402-1003美 元 價(jià)： $1019.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Targeted RNA Expression Kits enable highly customizable mid- to high-plex gene expression profiling studies. You can define panels of 12-1,000 assays to target individual exons, isoforms, splice junctions, coding SNPS (cSNPs), gene fusions, and non-coding RNA transcripts, plus multiplex up to 384 samples. Generate the data equivalent of up to 25,000 individual RT-PCR assays in a single run.* Assays include convenient online panel design and ordering, a rapid and simple workflow starting with as little as 50 ng of RNA, and automated, on-instrument data analysis. Types of Study Designs Custom panels—select up to 1000 targets from a database of over 400,000 predesigned assays. Add-on (supplemental) content—add a second oligo pool of up to 1000 targets to a previously designed TruSeq Targeted RNA Expression custom panel. Start a Custom Project Order custom panels using DesignStudio, a free, user-friendly, web-based tool. Simply select the assays you need and add them to your order, with no design time. Log in to DesignStudio Browse TruSeq Targeted RNA Sample Data Human Brain Reference RNA (HBRR), Universal Human Reference RNA (UHRR), and human liver RNA samples were prepared using the TruSeq Targeted RNA Expression Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 51 bp read length configuration. The total yield was 2.04 Gb with 96.5% of bases at or above Q30. Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub View TruSeq Targeted RNA Project Data (secondary analysis with BaseSpace Apps) *Refers to instruments with catalog number SY-410-1001 and upgrade, or catalog number SY-410-1003 Specifications: Assay Time 1 day Hands-On Time 4 hours Input Quantity 50 ng RNA,50 ng high-quality total RNA,≥ 200 ng FFPE total RNA; Recommended quantity may vary with expression level, target plexity, and sample quality Content Specifications Choose from 400,000+ pre-designed targeted RNA-Seq assays. Or add content to a fixed panel or previously designed custom panel. Multiplexing Up to 384 samples per sequencing run Mechanism of Action Amplification Method Targeted RNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Transcript Variants Specialized Sample Types FFPE | 1,019.00 |
| Illumina/TruSeq DNA Methylation Kit (96 reactions)/EGMK91396/1 Ea | EGMK91396 | Illumina | 產(chǎn)品編號(hào)： EGMK91396美 元 價(jià)： $5567.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: Unlock small samples (50–100 ng DNA input) CpG, CHH, & CHG regions included for comprehensive, whole-genome results Fast protocol – five-hour method Capture full sample diversity Sequence the entire sample–no loss of information The process of bisulfite treatment denatures genomic DNA into single stranded DNA. TruSeq DNA Methylation converts single stranded DNA into an Illumina sequencing library. All ssDNA fragments are captured into an Illumina sequencing library, therefore eliminating the loss of diversity associated with other methods. Supported analysis in the cloud TruSeq DNA Methylation libraries can be aligned to the human genome and compared for differential methylation with Illumina BaseSpace Apps MethylSeq and MethylKit. These applications are fully supported and were developed specifically for TruSeq DNA Methylation library preparation. Example data sets for TruSeq DNA Methylation libraries, also available in BaseSpace Sequence Hub Data Central (use the “Methyl Seq” category filter), demonstrate unparalleled quality and seamless analysis. Deep coverage of critical genomic regions Depth of coverage is enhanced in genomic areas with BIOLOGical utility. TruSeq DNA Methylation captures full sample diversity of critical areas, including: Coding region start and end for exons from the canonical transcript of protein coding genes for genes known to be involved in cancer, taken from SOMA and CRUK panels (as well as literature-derived cancer genes) Genes defined by the American College of Medical Genetics as being medically relevant (ACMG genes) Exonic coding regions from Ensemble 70 List of 100 promoters defined by the Broad Institute as being of high interest and difficult to sequence | 5,567.00 |
| Illumina/TruSeq Targeted RNA Index Kit (48 indexes, 48 samples)/RT-401-1001/1 Ea | RT-401-1001 | Illumina | 產(chǎn)品編號(hào)： RT-401-1001美 元 價(jià)： $698.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Targeted RNA Expression Kits enable highly customizable mid- to high-plex gene expression profiling studies. You can define panels of 12-1,000 assays to target individual exons, isoforms, splice junctions, coding SNPS (cSNPs), gene fusions, and non-coding RNA transcripts, plus multiplex up to 384 samples. Generate the data equivalent of up to 25,000 individual RT-PCR assays in a single run.* Assays include convenient online panel design and ordering, a rapid and simple workflow starting with as little as 50 ng of RNA, and automated, on-instrument data analysis. Types of Study Designs Custom panels—select up to 1000 targets from a database of over 400,000 predesigned assays. Add-on (supplemental) content—add a second oligo pool of up to 1000 targets to a previously designed TruSeq Targeted RNA Expression custom panel. Start a Custom Project Order custom panels using DesignStudio, a free, user-friendly, web-based tool. Simply select the assays you need and add them to your order, with no design time. Log in to DesignStudio Browse TruSeq Targeted RNA Sample Data Human Brain Reference RNA (HBRR), Universal Human Reference RNA (UHRR), and human liver RNA samples were prepared using the TruSeq Targeted RNA Expression Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 51 bp read length configuration. The total yield was 2.04 Gb with 96.5% of bases at or above Q30. Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub View TruSeq Targeted RNA Project Data (secondary analysis with BaseSpace Apps) *Refers to instruments with catalog number SY-410-1001 and upgrade, or catalog number SY-410-1003 Specifications: Assay Time 1 day Hands-On Time 4 hours Input Quantity 50 ng RNA,50 ng high-quality total RNA,≥ 200 ng FFPE total RNA; Recommended quantity may vary with expression level, target plexity, and sample quality Content Specifications Choose from 400,000+ pre-designed targeted RNA-Seq assays. Or add content to a fixed panel or previously designed custom panel. Multiplexing Up to 384 samples per sequencing run Mechanism of Action Amplification Method Targeted RNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Transcript Variants Specialized Sample Types FFPE | 698.00 |
| Illumina/TruSeq DNA Methylation Kit (24 reactions)/EGMK91324/1 Ea | EGMK91324 | Illumina | 產(chǎn)品編號(hào)： EGMK91324美 元 價(jià)： $1787.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: Unlock small samples (50–100 ng DNA input) CpG, CHH, & CHG regions included for comprehensive, whole-genome results Fast protocol – five-hour method Capture full sample diversity Sequence the entire sample–no loss of information The process of bisulfite treatment denatures genomic DNA into single stranded DNA. TruSeq DNA Methylation converts single stranded DNA into an Illumina sequencing library. All ssDNA fragments are captured into an Illumina sequencing library, therefore eliminating the loss of diversity associated with other methods. Supported analysis in the cloud TruSeq DNA Methylation libraries can be aligned to the human genome and compared for differential methylation with Illumina BaseSpace Apps MethylSeq and MethylKit. These applications are fully supported and were developed specifically for TruSeq DNA Methylation library preparation. Example data sets for TruSeq DNA Methylation libraries, also available in BaseSpace Sequence Hub Data Central (use the “Methyl Seq” category filter), demonstrate unparalleled quality and seamless analysis. Deep coverage of critical genomic regions Depth of coverage is enhanced in genomic areas with BIOLOGical utility. TruSeq DNA Methylation captures full sample diversity of critical areas, including: Coding region start and end for exons from the canonical transcript of protein coding genes for genes known to be involved in cancer, taken from SOMA and CRUK panels (as well as literature-derived cancer genes) Genes defined by the American College of Medical Genetics as being medically relevant (ACMG genes) Exonic coding regions from Ensemble 70 List of 100 promoters defined by the Broad Institute as being of high interest and difficult to sequence | 1,787.00 |
| Illumina/TruSeq Small RNA Set D MiniSeq Kit (1 library prep and 2 MiniSeq reagents)/20005616/1 Ea | 20005616 | Illumina | 產(chǎn)品編號(hào)： 20005616美 元 價(jià)： $3200.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Small RNA Library Preparation Kits provide reagents to generate small RNA libraries directly from total RNA. MicroRNAs (miRNAs) generated by Dicer processing are efficiently targeted by the included modified adapters. These kits enable multiplexed sequencing with the introduction of 48 unique indexes, allowing miRNA and small RNA discovery and profiling throughput to match the unparalleled output of Illumina sequencing. Indexes are added in a universal amplification reaction, greatly reducing ligation bias and ensuring accurate measurement of miRNA expression. Workflow improvements enable streamlined sample preparation, allowing economical studies covering all small RNA transcripts in any species. CompatIBLe applications include finding novel miRNAs, characterizing variation such as isomers with single-base resolution, and analyzing differential expression without prior assumptions. TruSeq Small RNA Sample Datasets The Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples were prepared using the TruSeq Small RNA Library Prep Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 36 bp read length configuration. The total yield was 0.91 Gb with 97% of bases at or above Q30. Browse the Data In BaseSpace Sequence Hub: View Run (primary analysis and metrics) View Project (secondary analysis with BaseSpace Apps) Specifications: Assay Time ~10.5 hours Hands-On Time ~30 minutes Input Quantity 25 to 100 ng total RNA from species with polyA tails Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails Multiplexing Up to 24-plex pooling with additional NeoPrep runs Sample Throughput Up to 16 samples per NeoPrep library card Species Category Drosophila,Any Species,Mouse,Zebrafish,Human,Rat,Plant,Nematode System Compatibility MiSeq,NextSeq 550,MiniSeq,NextSeq 500 Specialized Sample Types FFPE,Low Input Technology Sequencing Automation CapABIlity Liquid Handling Robots Variant Class Novel Transcripts,Transcript Variants Method miRNA and Small RNA Sequencing | 3,200.00 |
| Illumina/TruSeq DNA Methylation Index PCR Primers (10 reactions, 12 indexes)/EGIDX81312/1 Ea | EGIDX81312 | Illumina | 產(chǎn)品編號(hào)： EGIDX81312美 元 價(jià)： $78.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: Unlock small samples (50–100 ng DNA input) CpG, CHH, & CHG regions included for comprehensive, whole-genome results Fast protocol – five-hour method Capture full sample diversity Sequence the entire sample–no loss of information The process of bisulfite treatment denatures genomic DNA into single stranded DNA. TruSeq DNA Methylation converts single stranded DNA into an Illumina sequencing library. All ssDNA fragments are captured into an Illumina sequencing library, therefore eliminating the loss of diversity associated with other methods. Supported analysis in the cloud TruSeq DNA Methylation libraries can be aligned to the human genome and compared for differential methylation with Illumina BaseSpace Apps MethylSeq and MethylKit. These applications are fully supported and were developed specifically for TruSeq DNA Methylation library preparation. Example data sets for TruSeq DNA Methylation libraries, also available in BaseSpace Sequence Hub Data Central (use the “Methyl Seq” category filter), demonstrate unparalleled quality and seamless analysis. Deep coverage of critical genomic regions Depth of coverage is enhanced in genomic areas with BIOLOGical utility. TruSeq DNA Methylation captures full sample diversity of critical areas, including: Coding region start and end for exons from the canonical transcript of protein coding genes for genes known to be involved in cancer, taken from SOMA and CRUK panels (as well as literature-derived cancer genes) Genes defined by the American College of Medical Genetics as being medically relevant (ACMG genes) Exonic coding regions from Ensemble 70 List of 100 promoters defined by the Broad Institute as being of high interest and difficult to sequence | 78.00 |
| Illumina/TruSeq Bovine Parentage Kit (96 indexes, 96 samples)/20004795/1 Ea | 20004795 | Illumina | 產(chǎn)品編號(hào)： 20004795美 元 價(jià)： $960.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: This solution for parentage testing of multiple beef and dairy cattle breeds has added genotyping of relevant traits. By offering more information in a single assay than from parentage testing alone, service labs can use the TruSeq Bovine Parentage Sequencing Panel to make more informed herd management recommendations. Includes all International Society of Animal Genetics (ISAG) recommended content, plus disease-associated and economically relevant traits Content design, high accuracy, and reliABIlity eliminate need for multiple or repeat testing Analysis software converts sequencing results to genotype calls without the need for bioinformatics expertise The TruSeq Bovine Parentage Sequencing Panel uses proven Illumina next-generation sequencing (NGS) technology to deliver accurate genotyping results for SNP-based parentage determination in cattle. The high accuracy and reliABIlity of Illumina sequencing reduces the amount of required testing and shortens the time to answer, leADIng to efficiency gains and cost savings. It features a streamlined workflow that goes from DNA to report in 1.5 days with minimal hands-on time. Have confidence that the typing result is accurate, the first time. TruSeq Bovine Parentage has been tested with multiple breeds, DNA inputs, and extraction methods. It provides deep sequencing coverage across SNPs. Specifications: Input Quantity ≤ 1 ng genomic DNA, or 2 ul crude lysates, or 1.2 mm FTA card punch Hands-On Time ~1 hour Assay Time 9 hours Mechanism of Action PCR Multiplexing Maximum of 32 casework samples or 96 database or reference samples System Compatibility MiSeq Variant Class Single Nucleotide Polymorphisms (SNPs) Species Category Bovine Technology Sequencing Method Genotyping by Sequencing,Amplicon Sequencing,Targeted DNA Sequencing | 960.00 |
| Illumina/TruSeq Ribo Profile for Mammalian (12 reactions, 12 indexes)/RPHMR12126/1 Ea | RPHMR12126 | Illumina | 產(chǎn)品編號(hào)： RPHMR12126美 元 價(jià)： $1575.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: Study active mRNA translation with sequencing Sequence ribosome-protected mRNA Predict protein abundance Investigate translational control Measure gene expression Rapid, scalable spin-column method No ultracentrifuge required CompatIBLe with yeast and mammalian samples Sequence actively translated transcripts Ribosome profiling is a technique for investigating translational control that provides a snapshot of all the ribosomes active in a cell at a specific time. TruSeq Ribo Profile generates RNA-Seq libraries from ribosome-protected fragments of mRNAs that are actively being translated. Use TruSeq Ribo Profile to sequence mRNA fragments undergoing translation by ribosomes. These mRNA fragments are called "footprinted" or ribosome-protected mRNA fragments. You can also identify proteins being actively translated from samples prepared with TruSeq Ribo Profile. Samples collected at different times often show changes in translation. Samples treated with different drugs often show different translation patterns. Specifications: Input Quantity 0.1 – 1 ug high-quality purified total RNA from blood Content Specifications Captures coding RNA plus multiple forms of non-coding RNA Mechanism of Action Bead-based rRNA depletion, CDNA synthesis, and PCR Multiplexing Low-throughput kits: Pool up to 12 samples. Or pool up to 24 samples with sets A and B together,High-throughput kit version: Prepare 96 uniquely indexed samples System Compatibility NovaSeq 5000,Genome Analyzer IIx,HiSeq 2000,NextSeq 500,HiSeq 2500 Automation CapABIlity Liquid Handling Robots Variant Class Transcript Variants Species Category Rat | 1,575.00 |
| Illumina/TruSeq Small RNA Library Prep Kit -Set D (24 rxns) (Set D: indices 37-48)/RS-200-0048/1 Ea | RS-200-0048 | Illumina | 產(chǎn)品編號(hào)： RS-200-0048美 元 價(jià)： $2450.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Small RNA Library Preparation Kits provide reagents to generate small RNA libraries directly from total RNA. MicroRNAs (miRNAs) generated by Dicer processing are efficiently targeted by the included modified adapters. These kits enable multiplexed sequencing with the introduction of 48 unique indexes, allowing miRNA and small RNA discovery and profiling throughput to match the unparalleled output of Illumina sequencing. Indexes are added in a universal amplification reaction, greatly reducing ligation bias and ensuring accurate measurement of miRNA expression. Workflow improvements enable streamlined sample preparation, allowing economical studies covering all small RNA transcripts in any species. CompatIBLe applications include finding novel miRNAs, characterizing variation such as isomers with single-base resolution, and analyzing differential expression without prior assumptions. TruSeq Small RNA Sample Datasets The Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples were prepared using the TruSeq Small RNA Library Prep Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 36 bp read length configuration. The total yield was 0.91 Gb with 97% of bases at or above Q30. Browse the Data In BaseSpace Sequence Hub: View Run (primary analysis and metrics) View Project (secondary analysis with BaseSpace Apps) Specifications: Assay Time ~10.5 hours Hands-On Time ~30 minutes Input Quantity 25 to 100 ng total RNA from species with polyA tails Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails Multiplexing Up to 24-plex pooling with additional NeoPrep runs Sample Throughput Up to 16 samples per NeoPrep library card Species Category Drosophila,Any Species,Mouse,Zebrafish,Human,Rat,Plant,Nematode System Compatibility MiSeq,NextSeq 550,MiniSeq,NextSeq 500 Specialized Sample Types FFPE,Low Input Technology Sequencing Automation CapABIlity Liquid Handling Robots Variant Class Novel Transcripts,Transcript Variants Method miRNA and Small RNA Sequencing | 2,450.00 |
| Illumina/TruSeq Ribo Profile for Yeast (12 reactions, 12 indexes)/RPYSC12116/1 Ea | RPYSC12116 | Illumina | 產(chǎn)品編號(hào)： RPYSC12116美 元 價(jià)： $1575.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: Study active mRNA translation with sequencing Sequence ribosome-protected mRNA Predict protein abundance Investigate translational control Measure gene expression Rapid, scalable spin-column method No ultracentrifuge required CompatIBLe with yeast and mammalian samples Sequence actively translated transcripts Ribosome profiling is a technique for investigating translational control that provides a snapshot of all the ribosomes active in a cell at a specific time. TruSeq Ribo Profile generates RNA-Seq libraries from ribosome-protected fragments of mRNAs that are actively being translated. Use TruSeq Ribo Profile to sequence mRNA fragments undergoing translation by ribosomes. These mRNA fragments are called "footprinted" or ribosome-protected mRNA fragments. You can also identify proteins being actively translated from samples prepared with TruSeq Ribo Profile. Samples collected at different times often show changes in translation. Samples treated with different drugs often show different translation patterns. Specifications: Input Quantity 0.1 – 1 ug high-quality purified total RNA from blood Content Specifications Captures coding RNA plus multiple forms of non-coding RNA Mechanism of Action Bead-based rRNA depletion, CDNA synthesis, and PCR Multiplexing Low-throughput kits: Pool up to 12 samples. Or pool up to 24 samples with sets A and B together,High-throughput kit version: Prepare 96 uniquely indexed samples System Compatibility NovaSeq 5000,Genome Analyzer IIx,HiSeq 2000,NextSeq 500,HiSeq 2500 Automation CapABIlity Liquid Handling Robots Variant Class Transcript Variants Species Category Rat | 1,575.00 |
| Illumina/TruSeq Targeted RNA Index Kit B (96 indexes, 384 samples)/RT-402-1002/1 Ea | RT-402-1002 | Illumina | 產(chǎn)品編號(hào)： RT-402-1002美 元 價(jià)： $1019.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Targeted RNA Expression Kits enable highly customizable mid- to high-plex gene expression profiling studies. You can define panels of 12-1,000 assays to target individual exons, isoforms, splice junctions, coding SNPS (cSNPs), gene fusions, and non-coding RNA transcripts, plus multiplex up to 384 samples. Generate the data equivalent of up to 25,000 individual RT-PCR assays in a single run.* Assays include convenient online panel design and ordering, a rapid and simple workflow starting with as little as 50 ng of RNA, and automated, on-instrument data analysis. Types of Study Designs Custom panels—select up to 1000 targets from a database of over 400,000 predesigned assays. Add-on (supplemental) content—add a second oligo pool of up to 1000 targets to a previously designed TruSeq Targeted RNA Expression custom panel. Start a Custom Project Order custom panels using DesignStudio, a free, user-friendly, web-based tool. Simply select the assays you need and add them to your order, with no design time. Log in to DesignStudio Browse TruSeq Targeted RNA Sample Data Human Brain Reference RNA (HBRR), Universal Human Reference RNA (UHRR), and human liver RNA samples were prepared using the TruSeq Targeted RNA Expression Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 51 bp read length configuration. The total yield was 2.04 Gb with 96.5% of bases at or above Q30. Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub View TruSeq Targeted RNA Project Data (secondary analysis with BaseSpace Apps) *Refers to instruments with catalog number SY-410-1001 and upgrade, or catalog number SY-410-1003 Specifications: Assay Time 1 day Hands-On Time 4 hours Input Quantity 50 ng RNA,50 ng high-quality total RNA,≥ 200 ng FFPE total RNA; Recommended quantity may vary with expression level, target plexity, and sample quality Content Specifications Choose from 400,000+ pre-designed targeted RNA-Seq assays. Or add content to a fixed panel or previously designed custom panel. Multiplexing Up to 384 samples per sequencing run Mechanism of Action Amplification Method Targeted RNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Transcript Variants Specialized Sample Types FFPE | 1,019.00 |
| Illumina/HiSeq Rapid Duo cBot Sample Loading Kit/CT-403-2001/1 Ea | CT-403-2001 | Illumina | 產(chǎn)品編號(hào)： CT-403-2001美 元 價(jià)： $440.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.簇生成和測(cè)序試劑公司分類： Cluster Generation & Sequencing Reagents | Product Highlights: The HiSeq Rapid Duo cBot Sample LoADIng Kit allows maximum indexing freedom in rapid run mode by enabling individually addressable lanes. This kit is an optional accessory for HiSeq Rapid Cluster kits (which require a cBot instrument), and is designed for use in the rapid run workflow of HiSeq 2500 and 1500 sequencers. Load each flow cell lane independently Maximize indexing possibilities Separate precious samples physically Load different samples in each lane The HiSeq Rapid Duo cBot Sample LoADIng Kit allows each rapid flow cell lane to be loaded with a unique sample template pool. The duo kit accomplishes individual lane loADIng by allowing a cBot instrument to be used for the template hybridization and first extension steps of the cluster generation process. To use the cBot to load 2 libraries onto a rapid flow cell, 1 HiSeq Rapid Duo cBot Sample LoADIng Kit is required. Each kit contains sufficient reagents for loADIng 1 flow cell. A specifically designed duo manifold directs each of the 2 samples into the 2 separate rapid flow cell lanes. The cBot portion takes about an hour, after which the flow cell is moved to the HiSeq 2500 or 1500 for further cluster generation steps using a HiSeq Rapid Cluster Kit. | 440.00 |
| Illumina/PhiX Control v3/FC-110-3001/1 Ea | FC-110-3001 | Illumina | 產(chǎn)品編號(hào)： FC-110-3001美 元 價(jià)： $160.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.簇生成和測(cè)序試劑公司分類： Cluster Generation & Sequencing Reagents Size: 1 Ea | Product Highlights: PhiX Control v3 is a reliable, adapter-ligated library used as a control for Illumina sequencing runs. The library is derived from the small, well-characterized PhiX genome, offering several benefits for sequencing and alignment. The versatile PhiX Control v3 is provided as a ready-to-use library, and can be utilized in diverse applications to add value to your workflow and increase confidence in your results. The PhiX library provides a quality control for cluster generation, sequencing, and alignment, and a calibration control for cross-talk matrix generation, phasing, and prephasing. It can be rapidly aligned to estimate relevant sequencing by synthesis (SBS) metrics such as phasing and error rate. Depending on the application, PhiX Control v3 may also be utilized: As a high-concentration spike-in control for unbalanced samples (genomes with AT or GC content of less than 40% or greater than 60%) As a low-concentration spike-in control for alignment calculations and quantification efficiency As a dedicated control lane alongside low-diversity samples As a control for troubleshooting cluster generation problems, to help determine whether an error is related to library preparation Specifications: System Compatibility MiSeq,Genome Analyzer IIx,HiSeq 2000,HiSeq X Ten,HiScanSQ,NextSeq 550,HiSeq 3000,HiSeq X Five,HiSeq 1000,MiSeqDx in Research Mode,MiniSeq,HiSeq 1500,NextSeq 500,MiSeq FGx in Research Mode,HiSeq 2500,NovaSeq 6000,HiSeq 4000 Reagent Type Sequencing Control Technology Sequencing | 160.00 |
| Illumina/TruSeq Small RNA Set A MiniSeq Kit (1 library prep and 2 MiniSeq reagents)/20005613/1 Ea | 20005613 | Illumina | 產(chǎn)品編號(hào)： 20005613美 元 價(jià)： $3200.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: TruSeq Small RNA Library Preparation Kits provide reagents to generate small RNA libraries directly from total RNA. MicroRNAs (miRNAs) generated by Dicer processing are efficiently targeted by the included modified adapters. These kits enable multiplexed sequencing with the introduction of 48 unique indexes, allowing miRNA and small RNA discovery and profiling throughput to match the unparalleled output of Illumina sequencing. Indexes are added in a universal amplification reaction, greatly reducing ligation bias and ensuring accurate measurement of miRNA expression. Workflow improvements enable streamlined sample preparation, allowing economical studies covering all small RNA transcripts in any species. CompatIBLe applications include finding novel miRNAs, characterizing variation such as isomers with single-base resolution, and analyzing differential expression without prior assumptions. TruSeq Small RNA Sample Datasets The Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples were prepared using the TruSeq Small RNA Library Prep Kit. These libraries were sequenced on the MiniSeq System using the MiniSeq High Output Reagent Kit at a 1 x 36 bp read length configuration. The total yield was 0.91 Gb with 97% of bases at or above Q30. Browse the Data In BaseSpace Sequence Hub: View Run (primary analysis and metrics) View Project (secondary analysis with BaseSpace Apps) Specifications: Assay Time ~10.5 hours Hands-On Time ~30 minutes Input Quantity 25 to 100 ng total RNA from species with polyA tails Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails Multiplexing Up to 24-plex pooling with additional NeoPrep runs Sample Throughput Up to 16 samples per NeoPrep library card Species Category Drosophila,Any Species,Mouse,Zebrafish,Human,Rat,Plant,Nematode System Compatibility MiSeq,NextSeq 550,MiniSeq,NextSeq 500 Specialized Sample Types FFPE,Low Input Technology Sequencing Automation CapABIlity Liquid Handling Robots Variant Class Novel Transcripts,Transcript Variants Method miRNA and Small RNA Sequencing | 3,200.00 |
| Illumina | |||||
| Illumina/Infinium Accessory Starter Kit - Mid Throughput (110V)/WG-15-306/1 Ea | WG-15-306 | Illumina | 產(chǎn)品編號(hào)： WG-15-306美 元 價(jià)： $78000.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The Infinium iSelect offers the ABIlity to interrogate virtually any target (e.g. SNP, CNV, INDEL) across any species. Take advantage of the proven Infinium assay technology to create a fully-customized design that is tailored to your unique study needs. Design a custom genotyping panel that supports up to 700k custom targets (SNPs, indels, and CNVs). The Infinium iSelect can be deployed on either the 24-sample HD (3072 to 90,000 BeadTypes) or 24-sample HTS (90,001 to 700,000 BeadTypes). Creation of these custom assays enables focused, high-throughput genotyping applications tailored to specific project needs. Keep up-to-date with new discoveries by revising custom content through the Infinium iSelect + (add-on content) option. The Infinium iSelect+ option allows researchers to combine existing Marker sets with new, unique content to create a single BeadChip, thereby increasing the efficiency and cost-effectiveness of custom studies. Begin custom design and order process Specifications: Number of Markers iSelect HD: 3072 to 90,000 custom Markers,iSelect HTS: 90,000 to 700,000 custom Markers Sample Throughput Up to 5760 samples per week Input Quantity 200 ng Species Category Any Species Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 78,000.00 |
| Illumina/Infinium Multi-Ethnic AMR/AFR-8 v1.0 Kit (48 samples)/20001091/1 Ea | 20001091 | Illumina | 產(chǎn)品編號(hào)： 20001091美 元 價(jià)： $5232.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Infinium Multi-Ethnic AMR | Product Highlights: The Infinium Multi-Ethnic AMR/AFR-8 Kit provides a multi-purpose, multi-ethnic genotyping array focused on Hispanic and African American populations. With > 1.4 million expertly selected Markers, it enables identification of genetic associations with common and rare traits, providing insight to epidemiologists, health care researchers, population geneticists, and genomic researchers. Expert-selected content This kit combines expertly selected Markers and content from the most popular Illumina commercial arrays with the most current genomic information. Researchers can detect both common and rare variants across Hispanic and African American populations and impute variants in a vast number of subpopulations. Maximized imputation accuracy Consortium partners developed content for this multi-ethnic AMR/AFR genotyping array using tagging strategies with the power to perform more effective association studies in Hispanic and African American populations. The novel algorithm selects population-specific and transethnic tag SNPs that maximize imputation accuracy, as imputation has become a standard practice in the interpretation of genotyping data and allows for more accurate statistical inference of genotypes not directly genotyped. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 1,430,141u003cbru003eCustom Marker add-on capacity: Up to 245,000 Sample Throughput ~1067 samples per week Input Quantity 200 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 5,232.00 |
| Illumina/BovineLD v2.0 BeadChip (48 samples)/WG-451-2001/1 Ea | WG-451-2001 | Illumina | 產(chǎn)品編號(hào)： WG-451-2001美 元 價(jià)： $1200.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The BovineLD BeadChip microarray kit enables accurate genotyping to understand the impact of genetics on milk production, reproduction, health, and more. Delivering superior, scalable content at an economical price, it allows you to extend genomic selection to the entire herd. This array offers: A robust imputation tool to estimate genomic breeding value accurately High call rates, with demonstrated imputation efficiency of > 98% Expertly selected content that can be enhanced with up to 80,000 custom Markers Contains all 200 SNPs on the ISAG panel for bovine parentage (100 core SNPs and 100 additional SNPs) The ABIlity to interrogate up to 24 samples in parallel Cost-Effective Genotyping of Herd Animals The BovineLD v2.0 BeadChip, together with the Infinium BovineSNP50, Infinium BovineHD, and iSelect Custom BeadChips, creates a broad genotyping portfolio that breeders can rely on to characterize genetic variation and accurately estimate genomic breeding value. While the BovineHD and BovineSNP50 BeadChips provide superior power to interrogate genetic variation in high-value animals and support genome-wide studies, the BovineLD v2.0 BeadChip enables the cost-effective genotyping of lower-value animals. High Imputation Accuracy The BeadChip’s strategically selected SNPs possess demonstrated reliABIlity, high average minor allele frequency (MAF), uniform distribution across the bovine genome, and excellent imputation performance for a range of global dairy breeds. The 7,931 SNPs on the BovineLD v2.0 BeadChip were subjected to rigorous functional testing on multiple breeds to ensure strong performance. Illumina ensures that every BovineLD BeadChip offers > 99% average call rate across common dairy and beef cattle breeds. Superior, Scalable Content Illumina developed the BovineLD v2.0 BeadChip as part of a BovineLD Consortium in collaboration with global bovine agricultural thought leaders. Illumina scientists and collaborators referenced historical data generated with the BovineSNP50 BeadChip to identify the best SNP content for imputation efficiency among global dairy breeds.1 In silico testing determined that the highest imputation efficiency could be achieved by optimizing MAF among targeted breeds and evenly spacing SNPs across the entire bovine genome with higher Marker densities at the chromosomal ends. Content includes coverage of all chromosomes, including X, known Y haplotypes, and mitochondrial DNA. High-Throughput Format The Infinium Assay powers this multi-sample genotyping panel, delivering the industry’s highest call rates and reproducibility. The assay’s PCR-free single-tube sample preparation significantly reduces labor and potential sample handling errors.2,3 A multi-sample format further reduces experimental variABIlity and overall project cost by allowing breeders to interrogate up to 24 samples in parallel. Learn More About Plant and Animal Genotyping Specifications: Input Quantity 200 ng DNA (at 50 ng/ul) Number of Markers Fixed Markers: 7931 evenly spaced SNPs across the genomeu003cbru003eCustom Marker add-on capacity: Up to 80,000 (with + kit versions) Technology Microarray Species Category Bovine Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 1,200.00 |
| Illumina/Infinium® XT Upgrade Kit (24 Beadchips)/20011101/1 Ea | 20011101 | Illumina | 產(chǎn)品編號(hào)： 20011101美 元 價(jià)： $27531.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: Comprehensive Production-Scale Screening Solution This solution enables large-scale genetic improvement programs in agrigenomics and supports large-scale screening for biobanks and personalized medicine initiatives. It uses a high-efficiency, flexIBLe workflow. Production Scale: Optimized assay and 96-sample BeadChip enables processing of 100,000 to upwards of 1,000,000 samples/year per lab FlexIBLe Content: Targeted single or multispecies assays of 100s to 50,000 SNPs with at least 95% conversion rate guaranteed for custom panels High Efficiency Workflow: Total assay turnaround time reduced from 3 days to 2 days with less hands-on time Infinium XT simplifies the custom assay design process, reduces overall hands-on time, and enhances automation robot performance and utilization. The workflow offers an option to reduce the overall turnaround time, if the time to answer is more important than maximum weekly output. Streamlined Sample Preparation and Data Analysis A high-throughput solution like Infinium XT needs integrated systems that streamline sample preparation and analysis. The Illumina Automation Control software for the Tecan liquid handling robot has been updated to increase sample processing efficiency. An enhanced data analysis software solution offers real-time data generation and on-demand QC report functionality so production issues can be identified and corrected earlier in the process. Updated software for GenomeStudio speeds up genotype cluster generation, reducing overall analysis turnaround time. Also, a genotyping module for agricultural and other applications involving polyploid species is now included. After a cluster file is created, production-level analysis can be transitioned to Beeline Software. This software significantly reduces the time needed to observe quality performance specifications, generate genotyping reports, and analyze polyploid data, without removing the flexibility for manual intervention. Specifications: Sample Throughput 100,000 to u003e 1,000,000 samples/year Number of Markers 100s to 50,000 Markers of interest Species Category Any Species Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Insertions-Deletions (indels) Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 27,531.00 |
| Illumina/Infinium® Omni5Exome-4 v1.3 Kit (16 samples)/20005140/1 Ea | 20005140 | Illumina | 產(chǎn)品編號(hào)： 20005140美 元 價(jià)： $4448.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: Infinium Omni5Exome-4 BeadChip delivers comprehensive coverage of the genome, providing functional exonic content for whole-genome genotyping and copy number variation (CNV) analysis. The BeadChips include optimized tag SNPs targeting genetic variation down to 1% minor allele frequency (MAF). Using the proven iScan array scanner and integrated analysis software, these BeadChips offer optimized tag SNPs, exonic content, and fully supported CNV analysis. Combined with convenient packaging and a streamlined PCR-free protocol, these kits provide a comprehensive DNA analysis solution. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 4,548,474 Sample Throughput ~460 samples per week Input Quantity 400 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 4,448.00 |
| Illumina/Infinium ImmunoArray-24 v2 BeadChip Kit (1152 samples)/WG-357-1003/1 Ea | WG-357-1003 | Illumina | 產(chǎn)品編號(hào)： WG-357-1003美 元 價(jià)： $49536.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The Infinium ImmunoArray-24 v2 BeadChip is the next-generation genotyping array for detecting genetic variation in the human immune system. This BeadChip includes the most valuable content from the HumanImmuno v1 BeadChip, supplemented with newly selected content produced by the immunology research community. This new content includes the majority of the loci currently published in the GWAS catalog for major autoimmune and inflammatory disorders1 as well as published ancestry informative Markers. Valuable Content Infinium ImmunoArray-24 v2 BeadChip content highlights: Over 250,000 immune specific Markers Over 85,000 new Markers Includes most valuable content from HumanImmuno v1 BeadChip Focused on 17 major autoimmune disorders FlexIBLe Format The Infinium ImmunoArray-24 v2 can be tailored to incorporate up to ~390,000 custom beadtypes. This BeadChip is available as a standalone version as well as an add-on to several standard Illumina genotyping BeadChips. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: ~253,702,Custom Marker add-on capacity: Up to 390,000 (with + kit versions) Sample Throughput ~5760 samples per week Input Quantity 200 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Method Targeted Genotyping Array Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 49,536.00 |
| Illumina/Infinium OmniZhongHua-8 v1.3 Kit (96 samples)/20004339/1 Ea | 20004339 | Illumina | 產(chǎn)品編號(hào)： 20004339美 元 價(jià)： $10560.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The Infinium OmniZhongHua-8 BeadChip delivers exceptional coverage of common, intermediate, and rare variation found within Chinese populations for genome-wide association studies (GWAS). Optimized tag SNP content from all three HapMap phases and the 1000 Genomes Project (1kGP) has been strategically selected to create a population-focused array for the discovery of novel disease and trait associations in Chinese populations. The Infinium OmniZhongHua-8 BeadChip allows profiling of > 890,000 Markers per sample. The assay is deployed with proprietary BeadArray technology, delivering exceptionally high data quality with regards to call rates (average > 99%), reproducibility (> 99.9%), and low sample repeat rates. High signal-to-noise ratios and low overall noise levels allow for precise, reliable calls and copy number analyses. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 878,291,Custom Marker add-on capacity: None Sample Throughput ~960 samples per week Input Quantity 200 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 10,560.00 |
| Illumina/Infinium® Omni5Exome-4 v1.3 Kit (48 samples)/20005141/1 Ea | 20005141 | Illumina | 產(chǎn)品編號(hào)： 20005141美 元 價(jià)： $13344.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: Infinium Omni5Exome-4 BeadChip delivers comprehensive coverage of the genome, providing functional exonic content for whole-genome genotyping and copy number variation (CNV) analysis. The BeadChips include optimized tag SNPs targeting genetic variation down to 1% minor allele frequency (MAF). Using the proven iScan array scanner and integrated analysis software, these BeadChips offer optimized tag SNPs, exonic content, and fully supported CNV analysis. Combined with convenient packaging and a streamlined PCR-free protocol, these kits provide a comprehensive DNA analysis solution. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 4,548,474 Sample Throughput ~460 samples per week Input Quantity 400 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 13,344.00 |
| Illumina/Infinium® Omni5-4 v1.2 Kit (384 samples)/20005153/1 Ea | 20005153 | Illumina | 產(chǎn)品編號(hào)： 20005153美 元 價(jià)： $104832.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The Infinium Omni5-4 BeadChip delivers comprehensive coverage of the genome, leveraging powerful tagSNPs selected from the International HapMap and 1000 Genomes Projects that target genetic variation down to 1% minor allele frequency (MAF). Using the proven iScan System, this four-sample BeadChip offers high-throughput sample processing, and optimized content for whole-genome genotyping and CNV applications. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 4,284,426 Sample Throughput u003e460 samples per week Input Quantity 400 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 104,832.00 |
| Illumina/Infinium Multi-Ethnic EUR/EAS/SAS-8 v1.0 Kit (96 samples)/20001102/1 Ea | 20001102 | Illumina | 產(chǎn)品編號(hào)： 20001102美 元 價(jià)： $10464.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Infinium Multi-Ethnic EUR | Product Highlights: The Infinium Multi-Ethnic EUR/EAS/SAS-8 Kit provides a multi-purpose, multi-ethnic genotyping array focused on European, East Asian, and South Asian populations. With > 1.4 million expertly selected Markers, it enables identification of genetic associations with common and rare traits, providing insight to epidemiologists, health care researchers, population geneticists, and genomic researchers. Expert-selected content This kit combines expertly selected Markers and content from the most popular Illumina commercial arrays with the most current genomic information. Researchers can detect both common and rare variants across European, East Asian, and South Asian populations and impute variants in a vast number of subpopulations. Maximized imputation accuracy Consortium partners developed content for this multi-ethnic EUR/EAS/SAS genotyping array using tagging strategies with the power to perform more effective association studies in European, East Asian, and South Asian populations. The novel algorithm selects population-specific and transethnic tag SNPs that maximize imputation accuracy, as imputation has become a standard practice in the interpretation of genotyping data and allows for more accurate statistical inference of genotypes not directly genotyped. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 1,475,140u003cbru003eCustom Marker add-on capacity: Up to 245,000 Sample Throughput ~1067 samples per week Input Quantity 200 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 10,464.00 |
| Illumina/Infinium Exome-24 v1.1 Kit (48 samples)/20015246/1 Ea | 20015246 | Illumina | 產(chǎn)品編號(hào)： 20015246美 元 價(jià)： $2256.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: Infinium Exome-24 BeadChip delivers exceptional coverage of putative functional exonic variants selected from over 12,000 individual exome and whole-genome sequences. Markers were identified through a close collaboration with leADIng geneticists with the goal of developing an extensive catalog of exome variants. The exonic content consists of >240,000 Markers representing diverse populations - including European, African, Chinese, and Hispanic individuals - and a range of common conditions, such as type 2 diabetes, cancer, metabolic, and psychiatric disorders. Infinium Exome-24 BeadChip delivers focused coverage of exonic regions, but does not include coverage outside of coding regions. For greater flexibility, the Infinium Exome-24+ version of the BeadChip can be customized to include up to 400,000 additional Markers. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 244,883,Custom Marker add-on capacity: Up to 400,000 (with + kit versions) Sample Throughput ~2304 samples per week Input Quantity 200 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 2,256.00 |
| Illumina/MaizeSNP50 BeadChip (288 samples)/WG-500-1002/1 Ea | WG-500-1002 | Illumina | 產(chǎn)品編號(hào)： WG-500-1002美 元 價(jià)： $14400.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The MaizeSNP50 DNA Analysis Kit enables the interrogation of genetic variation across maize lines. Illumina developed this BeadChip array in collaboration with TraitGenetics, the French National Institute for Agricultural Research (INRA), and Syngenta, with the SNP content selected from several public and private sources. This BeadChip contains more than 50,000 validated Markers derived from the B73 reference sequence. The highly polymorphic SNP content on the MaizeSNP50 BeadChip was subjected to rigorous functional testing across over 30 diverse maize lines to ensure strong performance. Importantly, this BeadChip presents an average of greater than 25 Markers per megabase (Mb), providing ample SNP density for robust whole-genome genotyping studies. In addition, the MaizeSNP50 Marker set increases the ABIlity to perform corn genetic mapping and Marker assisted breeding. The MaizeSNP50 BeadChip provides high call rates and allows for flexIBLe content deployment. The assay's single-tube sample preparation without PCR or ligation steps significantly reduces labor and potential sample handling errors The BeadChip further reduces experimental variABIlity by allowing researchers to interrogate up to 24 samples in parallel For a low-density option, see the MaizeLD BeadChip Kit. Learn More About Plant and Animal Genotyping Specifications: Input Quantity 200 ng at 50 ng/µl Number of Markers Fixed Markers: 56,110 evenly distributed SNPs across the genomeu003cbru003eCustom Marker add-on capacity: None Method Genome-Wide Genotyping Array Technology Microarray Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan Species Category Maize | 14,400.00 |
| Illumina/Infinium CoreExome-24 v1.2 Kit (1152 samples)/20015264/1 Ea | 20015264 | Illumina | 產(chǎn)品編號(hào)： 20015264美 元 價(jià)： $62208.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The customizable Infinium CoreExome-24 BeadChip offers an economical way to perform and support large genetic studies, especially large-scale genotyping studies. They can also be used to quickly and easily obtain baseline sample data sets for a variety of downstream applications, including common variant, sex confirmation, mtDNA, ancestry, loss-of-variant, indel, and CNV studies. Developed in collaboration with several leADIng research institutions, the Infinium CoreExome-24 BeadChip includes all the tag SNPs found on the Infinium Core-24 BeadChip, plus over 240,000 Markers from the Infinium Exome-24 BeadChip. For greater flexibility, the Infinium CoreExome-24+ version of the BeadChip can be customized to include up to 100,000 additional Markers. The Infinium CoreExome-24 BeadChips use the Infinium high-throughput screening (HTS) 24-sample format, enabling high content flexibility, throughput capacity, and genotyping accuracy. When combined with the proven iScan System, these BeadChips deliver affordable, high-quality, genome-wide information across diverse world populations. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 550,601,Custom Marker add-on capacity: Up to 100,000 (with + kit versions) Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 62,208.00 |
| Illumina/Infinium Core-24 Kit v1.1 (48 samples)/20015254/1 Ea | 20015254 | Illumina | 產(chǎn)品編號(hào)： 20015254美 元 價(jià)： $2352.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The customizable Infinium Core-24 BeadChip offers an economical way to perform and support large genetic studies. Developed in collaboration with several leADIng research institutions, the Infinium Core-24 BeadChip contains highly-informative genome-wide tag SNPs found across diverse world populations, additional high-value Markers (including indels and updated exome-focused content), and has capacity to include up to 300,000 semi-custom Markers. In addition to cost-effectively performing large-scale genotyping studies, this BeadChip can be used to quickly and easily obtain baseline sample datasets for a variety of downstream applications, including common variant, mtDNA, ancestry, sex confirmation, loss-of-variant, indel, and CNV detection studies. The Infinium Core-24 BeadChip is based upon the trusted Infinium assay. Using the proven iScan System, this 24-sample BeadChip combines affordABIlity with high-throughput sample processing to deliver high-quality, genome-wide information. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 307,342,Custom Marker add-on capacity: Up to 300,000 (with + kit versions) Sample Throughput 2304 samples per week Input Quantity 200 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 2,352.00 |
| Illumina/CanineHD BeadChip (1152 samples)/WG-440-1003/1 Ea | WG-440-1003 | Illumina | 產(chǎn)品編號(hào)： WG-440-1003美 元 價(jià)： $97920.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: Featuring highly polymorphic single-nucleotide polymorphism (SNP) content and providing uniform genomic coverage, the CanineHD BeadChip array enables the interrogation of genetic variation in any domestic dog breed. Importantly, this BeadChip presents an average of greater than 70 Markers per megabase (Mb), providing ample SNP density for robust within-breed association and copy number variation (CNV) studies. This BeadChip contains more than 170,000 Markers placed on the CanFam2.0 reference sequence. Illumina developed this array in collaboration with the LUPA Consortium, which includes 22 European universities and other partners such as the Broad Institute. Learn More About Animal and Plant Genotyping Specifications: Input Quantity 200 ng DNA (at 50 ng/ul) Number of Markers Fixed Markers: 172,115 evenly spaced SNPs across the genome Method Genome-Wide Genotyping Array Technology Microarray Specialized Sample Types FFPE Species Category Canine Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 97,920.00 |
| Illumina/Infinium OncoArray-500K BeadChip Kit (1152 samples) 500,000 loci. Each package contains 48 BeadChips, along wit | WG-355-1003 | Illumina | 產(chǎn)品編號(hào)： WG-355-1003美 元 價(jià)： $74880.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The Infinium OncoArray-500K contains 500,000 SNPs with a genome-wide backbone of 250,000 tag SNPs. Additional SNPs include genetic variants associated with breast, colorectal, lung, ovarian, and prostate cancers plus SNPs covering ancestry, quantitative traits, pharmacogenetics, and fine-mapping of common cancer susceptibility loci. To support additional research requirements, the Infinium OncoArray-500K can be tailored to incorporate up to 120,000 custom beadtypes.* The Infinium OncoArray-500K was developed in collaboration with leADIng experts from the OncoArray consortium†, and draws on many of the features of the successful Collaborative Oncological Gene-environment Study (iCOGS) array1. Designed with candidate SNPs identified by the consortium, the OncoArray provides a cost-effective means to assess candidate variants potentially associated with cancer risk. The Infinium OncoArray-500K uses a 24-sample high-throughput screening (HTS) BeadChip to enable maximum throughput, productivity, and genotyping accuracy. Using the proven iScan System, the Infinium OncoArray-500K is designed to combine affordABIlity with high-density content, providing insight into the relationship between gene variants and cancer predisposition in five of the most prevalent cancers. * For additional information about custom add-on content, contact your Illumina account manager or sales specialist. Learn More About Human Genotyping Specifications: Input Quantity 200 ng DNA Sample Throughput ~2,304 samples per week Number of Markers Fixed Markers: ~500,000u003cbru003e Custom Marker add-on capacity: Up to 120,000 (with + kit versions) Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 74,880.00 |
| Illumina/PorcineSNP60v2 BeadChip (1152 samples)/WG-410-2003/1 Ea | WG-410-2003 | Illumina | 產(chǎn)品編號(hào)： WG-410-2003美 元 價(jià)： $57600.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The PorcineSNP60 DNA Analysis Kit v2 features 65,000 evenly spaced probes, offering more than sufficient SNP density for whole-genome association studies, determination of genetic merit, identification of quantitative trait loci, and comparative genetic studies. This 24-sample BeadChip presents a solution for interrogating genetic variation in multiple porcine breeds, including Duroc, Landrace, Pietran, and Large White. A semi-custom version of the BeadChip, the PorcineSNP60+ DNA Analysis Kit v2, allows researchers to include up to 25,000 additional custom probes for targeted studies. The Porcine SNP Chip Consortium made the final selection of the highest quality Markers from more than 510,000 single nucleotide polymorphisms (SNPs), after combining novel discovered SNPs with several other existing databases and study results. The panel was optimized using multiple criteria for Marker selection, including minor allele frequency determined from representative sample sequencing, allele count, quality score, spacing, location, and validation status. Learn More About Plant and Animal Genotyping Specifications: Input Quantity 200 ng DNA Number of Markers Fixed Markers: 64,232u003cbru003eCustom Marker add-on capacity: Up to 25,000 (with + kit versions) Method Genome-Wide Genotyping Array Technology Microarray Specialized Sample Types FFPE Species Category Porcine Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 57,600.00 |
| Illumina/Infinium® Omni5Exome-4 v1.3 Kit (96 samples)/20005142/1 Ea | 20005142 | Illumina | 產(chǎn)品編號(hào)： 20005142美 元 價(jià)： $26688.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: Infinium Omni5Exome-4 BeadChip delivers comprehensive coverage of the genome, providing functional exonic content for whole-genome genotyping and copy number variation (CNV) analysis. The BeadChips include optimized tag SNPs targeting genetic variation down to 1% minor allele frequency (MAF). Using the proven iScan array scanner and integrated analysis software, these BeadChips offer optimized tag SNPs, exonic content, and fully supported CNV analysis. Combined with convenient packaging and a streamlined PCR-free protocol, these kits provide a comprehensive DNA analysis solution. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 4,548,474 Sample Throughput ~460 samples per week Input Quantity 400 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 26,688.00 |
| Illumina/Infinium Exome-24 v1.1 Kit (288 samples)/20015247/1 Ea | 20015247 | Illumina | 產(chǎn)品編號(hào)： 20015247美 元 價(jià)： $13536.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: Infinium Exome-24 BeadChip delivers exceptional coverage of putative functional exonic variants selected from over 12,000 individual exome and whole-genome sequences. Markers were identified through a close collaboration with leADIng geneticists with the goal of developing an extensive catalog of exome variants. The exonic content consists of >240,000 Markers representing diverse populations - including European, African, Chinese, and Hispanic individuals - and a range of common conditions, such as type 2 diabetes, cancer, metabolic, and psychiatric disorders. Infinium Exome-24 BeadChip delivers focused coverage of exonic regions, but does not include coverage outside of coding regions. For greater flexibility, the Infinium Exome-24+ version of the BeadChip can be customized to include up to 400,000 additional Markers. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 244,883,Custom Marker add-on capacity: Up to 400,000 (with + kit versions) Sample Throughput ~2304 samples per week Input Quantity 200 ng DNA Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 13,536.00 |
| Illumina/Infinium CoreExome-24 v1.2 Kit (288 samples)/20015263/1 Ea | 20015263 | Illumina | 產(chǎn)品編號(hào)： 20015263美 元 價(jià)： $15552.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Microarray Kits | Product Highlights: The customizable Infinium CoreExome-24 BeadChip offers an economical way to perform and support large genetic studies, especially large-scale genotyping studies. They can also be used to quickly and easily obtain baseline sample data sets for a variety of downstream applications, including common variant, sex confirmation, mtDNA, ancestry, loss-of-variant, indel, and CNV studies. Developed in collaboration with several leADIng research institutions, the Infinium CoreExome-24 BeadChip includes all the tag SNPs found on the Infinium Core-24 BeadChip, plus over 240,000 Markers from the Infinium Exome-24 BeadChip. For greater flexibility, the Infinium CoreExome-24+ version of the BeadChip can be customized to include up to 100,000 additional Markers. The Infinium CoreExome-24 BeadChips use the Infinium high-throughput screening (HTS) 24-sample format, enabling high content flexibility, throughput capacity, and genotyping accuracy. When combined with the proven iScan System, these BeadChips deliver affordable, high-quality, genome-wide information across diverse world populations. Learn More About Human Genotyping Specifications: Number of Markers Fixed Markers: 550,601,Custom Marker add-on capacity: Up to 100,000 (with + kit versions) Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE Species Category Human Automation CapABIlity Liquid Handling Robots,Autoloader 2.x Array Loader System Compatibility iScan | 15,552.00 |
| Illumina/BaseSpace Sequence Hub Enterprise Annual Subscription/SW-411-1003/1 Ea | SW-411-1003 | Illumina | 產(chǎn)品編號(hào)： SW-411-1003美 元 價(jià)： $29995.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Informatics Products | Product Highlights: As a key component of the BaseSpace Suite, BaseSpace Sequence Hub is a direct extension of your Illumina instruments. Data flows directly from the instrument into BaseSpace Sequence Hub, which enables you to manage and analyze data using a curated set of analysis apps. BaseSpace Sequence Hub: Enables you to set up and monitor instrument runs in real-time Promotes efficiency by converting sequencing data to a standard format and directly streaming them to the cloud Provides a more economical solution than assembling infrastructures and tools in-house Increases productivity with easy access and execution of a multitude of genomic analysis apps (provided by you, Illumina, or third-parties). As a result, specialized staff members, such as bioinformaticians are free to work on more complicated analyses Fosters collaboration and innovation with simplified data sharing Provides multiple layers of security and supports Health Insurance PortABIlity and AccountABIlity Act (HIPAA) compliance using robust Amazon Web Services cloud infrastructure Scales to accommodate the need for more storage and computing with a tiered pricing structure See All BaseSpace Data Analysis Apps Visit the BaseSpace Suite Blog | 29,995.00 |
| Illumina/SureRef Reference Female DNA (128 μl)/PR-40-415204-00/1 Ea | PR-40-415204-00 | Illumina | 產(chǎn)品編號(hào)： PR-40-415204-00美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The SureRef Pack contains both SureRef Reference Male DNA and SureRef Reference Female DNA, each sufficient for 16 reference labeling reactions. The individual DNAs are also available separately. SureRef DNA products are matched, in terms of quality and size of DNA fragment to a single cell or a few cells. Extracted DNA should be amplified with the SurePlex DNA Amplification System and used as part of 24sure laboratory product protocols. | 0.00 |
| Illumina/VeriSeq™ PGS Kit - MiSeq®/RH-101-1001/1 Ea | RH-101-1001 | Illumina | 產(chǎn)品編號(hào)： RH-101-1001美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The VeriSeq PGS Kit takes advantage of next-generation sequencing (NGS) technology to provide comprehensive, accurate screening of all 24 chromosomes for selection of embryos most likely to be euploid. Preimplantation genetic screening (PGS) results generated using VeriSeq PGS are comparable to those achieved with the widely used array-based 24sure technology. In addition, NGS offers the opportunity for improved assay workflow, higher throughput, and enhanced performance.1 Industry-leADIng data quality: More than 90% of the world’s sequencing data is generated by Illumina sequencing by synthesis (SBS) chemistry* Fast, streamlined workflow: Sample to answer in approximately 12 hours High-throughput analysis: Screen up to 24 samples per run Ultra-Low Input NGS offers a highly sensitive method for screening embryos, requiring as little as 1 ng of DNA from a SurePlex DNA amplification reaction. DNA can be obtained from a blastomere biopsy, from a day 3 embryo, or from a trophectodermal (TE) biopsy from a blastocyst. *Data calculations on file. Illumina, Inc., 2015. Specifications: Assay Time 11 hours Hands-On Time 4 hours Input Quantity 30 to 300 ng depending on QC results System Compatibility MiSeq,MiSeqDx in Research Mode Method PGS Sequencing Technology Sequencing Specialized Sample Types Single Cells Species Category Human Variant Class Chromosomal Abnormalities,Structural Variants,Copy Number Variants (CNVs) | 0.00 |
| Illumina/Infinium CytoSNP-850K v1.1 BeadChip Kit (48 samples)/WG-322-1103/1 Ea | WG-322-1103 | Illumina | 產(chǎn)品編號(hào)： WG-322-1103美 元 價(jià)： $12000.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The Infinium CytoSNP-850K v1.1 BeadChip is the first SNP-based human microarray to leverage the latest input from the international community for cytogenomics studies. The gene list was defined based on content from the International Collaboration for Clinical Genomics (ICCG)1 and the Cancer Genomics Consortium (CGC)2, providing a comprehensive view of cytogenomic activity.* This enhanced SNP coverage enables copy number calls as small as 10 kb in regions associated with genetic disease. Thorough Coverage for Constitutional and Cancer Applications The Infinium CytoSNP-850K v1.1 BeadChip provides comprehensive coverage of cytogenetically relevant genes on a proven platform, helping researchers find valuable information that may be missed by other technologies. It contains approximately 850,000 empirically selected single nucleotide polymorphisms (SNPs) spanning the entire genome with enriched coverage for 3,262 genes of known cytogenetics relevance in both constitutional and cancer applications. High Detection Sensitivity for Low-level Mosaics A unique attribute of the Infinium array technology is the use of long 50-mer probes that have high specificity to the SNP target. This increases sensitivity for low-level mosaics3 and offers high resolution for copy-neutral loss of heterozygosity (LOH). In addition, each SNP is represented in at least 15x redundancy to increase the signal-to-noise ratio for making accurate copy number variation (CNV) and absence of heterozygosity (AOH) calls across the genome. As few as 10 consecutive probes are necessary to make accurate CNV calls, demonstrating the high performance level of the Infinium assay. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,6 hours 15 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) Specialized Sample Types FFPE System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 12,000.00 |
| Illumina/Infinium CytoSNP-850K v1.1 BeadChip Kit (96 samples)/WG-322-1104/1 Ea | WG-322-1104 | Illumina | 產(chǎn)品編號(hào)： WG-322-1104美 元 價(jià)： $24000.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The Infinium CytoSNP-850K v1.1 BeadChip is the first SNP-based human microarray to leverage the latest input from the international community for cytogenomics studies. The gene list was defined based on content from the International Collaboration for Clinical Genomics (ICCG)1 and the Cancer Genomics Consortium (CGC)2, providing a comprehensive view of cytogenomic activity.* This enhanced SNP coverage enables copy number calls as small as 10 kb in regions associated with genetic disease. Thorough Coverage for Constitutional and Cancer Applications The Infinium CytoSNP-850K v1.1 BeadChip provides comprehensive coverage of cytogenetically relevant genes on a proven platform, helping researchers find valuable information that may be missed by other technologies. It contains approximately 850,000 empirically selected single nucleotide polymorphisms (SNPs) spanning the entire genome with enriched coverage for 3,262 genes of known cytogenetics relevance in both constitutional and cancer applications. High Detection Sensitivity for Low-level Mosaics A unique attribute of the Infinium array technology is the use of long 50-mer probes that have high specificity to the SNP target. This increases sensitivity for low-level mosaics3 and offers high resolution for copy-neutral loss of heterozygosity (LOH). In addition, each SNP is represented in at least 15x redundancy to increase the signal-to-noise ratio for making accurate copy number variation (CNV) and absence of heterozygosity (AOH) calls across the genome. As few as 10 consecutive probes are necessary to make accurate CNV calls, demonstrating the high performance level of the Infinium assay. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,6 hours 15 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) Specialized Sample Types FFPE System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 24,000.00 |
| Illumina/24sure Microarray Pack (16 hybridizations, up to 32 samples)/PR-10-408702-PK/1 Ea | PR-10-408702-PK | Illumina | 產(chǎn)品編號(hào)： PR-10-408702-PK美 元 價(jià)： $3530.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Preimplantation genetic screening (PGS) with 24sure microarrays provides a comprehensive and accurate assessment of all 24 chromosomes from an embryo biopsy. The arrays can be used to screen for aneuploidy in first and second polar bodies, blastomere biopsies, and trophectoderm biopsies. The 24sure assay is objective, ensuring a high degree of confidence in the results and subsequent selection of embryos least likely to have aneuploidy for transfer. Widely used, proven PGS – Method of choice for many of the world’s reference laboratories Fast, reliable results – Comprehensive, accurate assessment of all 24 chromosomes in 12 hours Straightforward workflow – Optimized protocols include minimal tube transfers, documented quality control (QC) stages, and flexIBLe stopping points Straightforward Workflow Is Complete in 12 Hours The straightforward 24sure protocol used standard laboratory techniques, providing a fast, accurate method for chromosome screening with minimal sensitivity to technical errors and designed to fit into existing workflows. Screening can be completed in 12 hours, and therefore does not interfere with tight schedules of a fresh IVF cycle. Specifications: Assay Time ~12 hours Hands-On Time ~2.5 hours Input Quantity Single cell or multi-cell samples Technology Microarray Specialized Sample Types Single Cells Species Category Human Variant Class Chromosomal Abnormalities,Structural Variants,Copy Number Variants (CNVs) Method PGS Array Significantly Higher Rate of Pregnancy May Be PossIBLe with PGS: The pregnancy rate shown for embryos analyzed using preimplantation genetic screening and morphology is 69.1%, much higher than the 41.7% achieved using morphology screening alone.1 Pilot study of young, good prognosis patients (age < 35, first-time IVF, no history of prior miscarriage, n = 103). PGS with 24sure Arrays Reduces the Effect of Maternal Age on Implantation and Pregnancy Rates: Although aneuploidy risk increases with maternal age, PGS using 24sure arrays on either day 3 or day 5 embryos diminishes the effect of maternal age on implantation and pregnancy rates.2 24Sure Laboratory Workflow: The 24sure laboratory workflow is a straightforward procedure that is completed in <12 hours. BlueFuse Multi Software Delivers a Complete Data Analysis and Information Management System: BlueFuse Multi Software provides a complete solution for analyzing, storing, and reporting 24sure results. A. Sample database displays experimental information. B. Array images imported directly from the scanner. C. Profiles for sample and reference chromosomes. D. Automated cycle reports. | 3,530.00 |
| Illumina/HumanCytoSNP FFPE-12 v2.1 DNA Analysis BeadChip Kit (24 samples) 250,000 loci. Each package contains 2 BeadChip | WG-321-1003 | Illumina | 產(chǎn)品編號(hào)： WG-321-1003美 元 價(jià)： $3720.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The HumanCytoSNP FFPE-12 BeadChip interrogates >262,000 genomic Markers. The content consists of intelligently selected tag SNPs that provide comprehensive genomic coverage. With dense and even Marker spacing, the BeadChip content can also be used to precisely detect structural aberrations, allowing researchers to accurately identify structural differences between paired-normal and tumor samples. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,2 hours 10 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) Specialized Sample Types FFPE System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 3,720.00 |
| Illumina/24sure+ Pack (16 samples)/PR-10-408602-PK/1 Ea | PR-10-408602-PK | Illumina | 產(chǎn)品編號(hào)： PR-10-408602-PK美 元 價(jià)： $4460.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The 24sure+ microarray is designed to improve the success of in vitro fertilization (IVF) by detecting subchromosomal imbalances in embryos of reciprocal translocation carriers. 24sure+ includes increased coverage of pericentromeric and subtelomeric regions to ensure the identification and reporting of small derived chromosome fragments from single cells. 24sure+ microarrays offer several key advantages: 24sure+ can more accurately determine balanced or euploid embryos for selection compared to trADItional fluorescent in situ hybridization (FISH) methods1 Rapid workflow enables sample results and reporting within 12 hours Every 24sure+ purchase includes BlueFuse Multi software for the fully automated analysis, interpretation, and reporting of 24sure+ investigations 24sure+ analysis is ideally offered to couples undergoing IVF due to recurrent miscarriages sUSPected to be caused by the presence of a balanced translocation in either parent. Balanced translocation carriers may not present with a phenotype. However, segregation of the translocated chromosomes during gamete formation can produce a range of normal, balanced, and unbalanced gametes, with unbalanced products expected to represent 50% of gametes.2 Resulting embryos with large structural imbalances are likely to be non-viable. As a result, the balanced carrier may present with infertility or a history of recurrent miscarriage/spontaneous abortion.3 Couples presenting with recurrent miscarriage can be karyotyped, which is a low-resolution analysis that may determine whether the problems they are experiencing are due to a balanced rearrangement. If this is the case, such carriers of balanced translocations may seek 24sure+ analysis of embryos. Specifications: Assay Time ~12 hours Hands-On Time ~3.5 hours Input Quantity SurePlex whole-genome-amplified single cells from embryo biopsies Technology Microarray Method PGD Array Specialized Sample Types Single Cells Species Category Human Variant Class Chromosomal Abnormalities | 4,460.00 |
| Illumina/HumanCytoSNP-12 v2.1 BeadChip Kit (12 samples)/WG-320-2101/1 Ea | WG-320-2101 | Illumina | 產(chǎn)品編號(hào)： WG-320-2101美 元 價(jià)： $1860.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The 12-sample HumanCytoSNP-12 BeadChip is a powerful, whole-genome scanning panel designed for efficient, high-throughput analysis of genetic and structural variations that are most relevant to human disease. This scalable, proven solution offers substantially better resolution to detect smaller regions than fluorescence in situ hybridization (FISH) or comparative genomic hybridization (CGH).1 Complete panel of genome-wide tag single nucleotide polymorphisms (SNPs) and Markers targeting all regions of known cytogenetic importance, incorporating ~300,000 “best of the best” SNPs with the highest tagging power Average SNP call rates and reproducibility of > 99.9%, and low noise for copy number measurements Detect many types and sizes of structural variation in the human genome that affect phenotypes, including duplications, deletions, amplifications, copy-neutral loss of heterozygosity (LOH), and mosaicism Process up to 12 samples in parallel, increasing sample throughput and decreasing experimental variABIlity Process samples using the single-tube, PCR-free Infinium HD Assay that requires only 200ng DNA per sample Comprehensive data analysis with intuitive BlueFuse Multi Software streamlines copy number assessment and results reporting The HumanCytoSNP-12 BeadChip is optimized to detect cytogenetic abnormalities most relevant to human disease.1-2 Content includes ~300,000 SNPs targeting regions shown to be important for cytogenetic analysis. The result is dense coverage of ~250 disease regions, including subtelomeric regions, pericentromeric regions, and sex chromosomes, commonly screened in cytogenetics labs. Sufficient SNP coverage is provided to determine dosage sensitivity of > 800 genes. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,6 hours 15 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 1,860.00 |
| Illumina/Infinium CytoSNP-850K v1.1 BeadChip Kit (8 samples)/WG-322-1101/1 Ea | WG-322-1101 | Illumina | 產(chǎn)品編號(hào)： WG-322-1101美 元 價(jià)： $2000.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The Infinium CytoSNP-850K v1.1 BeadChip is the first SNP-based human microarray to leverage the latest input from the international community for cytogenomics studies. The gene list was defined based on content from the International Collaboration for Clinical Genomics (ICCG)1 and the Cancer Genomics Consortium (CGC)2, providing a comprehensive view of cytogenomic activity.* This enhanced SNP coverage enables copy number calls as small as 10 kb in regions associated with genetic disease. Thorough Coverage for Constitutional and Cancer Applications The Infinium CytoSNP-850K v1.1 BeadChip provides comprehensive coverage of cytogenetically relevant genes on a proven platform, helping researchers find valuable information that may be missed by other technologies. It contains approximately 850,000 empirically selected single nucleotide polymorphisms (SNPs) spanning the entire genome with enriched coverage for 3,262 genes of known cytogenetics relevance in both constitutional and cancer applications. High Detection Sensitivity for Low-level Mosaics A unique attribute of the Infinium array technology is the use of long 50-mer probes that have high specificity to the SNP target. This increases sensitivity for low-level mosaics3 and offers high resolution for copy-neutral loss of heterozygosity (LOH). In addition, each SNP is represented in at least 15x redundancy to increase the signal-to-noise ratio for making accurate copy number variation (CNV) and absence of heterozygosity (AOH) calls across the genome. As few as 10 consecutive probes are necessary to make accurate CNV calls, demonstrating the high performance level of the Infinium assay. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,6 hours 15 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) Specialized Sample Types FFPE System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 2,000.00 |
| Illumina/Infinium CytoSNP-850K v1.1 BeadChip Kit (16 samples)/WG-322-1102/1 Ea | WG-322-1102 | Illumina | 產(chǎn)品編號(hào)： WG-322-1102美 元 價(jià)： $4000.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The Infinium CytoSNP-850K v1.1 BeadChip is the first SNP-based human microarray to leverage the latest input from the international community for cytogenomics studies. The gene list was defined based on content from the International Collaboration for Clinical Genomics (ICCG)1 and the Cancer Genomics Consortium (CGC)2, providing a comprehensive view of cytogenomic activity.* This enhanced SNP coverage enables copy number calls as small as 10 kb in regions associated with genetic disease. Thorough Coverage for Constitutional and Cancer Applications The Infinium CytoSNP-850K v1.1 BeadChip provides comprehensive coverage of cytogenetically relevant genes on a proven platform, helping researchers find valuable information that may be missed by other technologies. It contains approximately 850,000 empirically selected single nucleotide polymorphisms (SNPs) spanning the entire genome with enriched coverage for 3,262 genes of known cytogenetics relevance in both constitutional and cancer applications. High Detection Sensitivity for Low-level Mosaics A unique attribute of the Infinium array technology is the use of long 50-mer probes that have high specificity to the SNP target. This increases sensitivity for low-level mosaics3 and offers high resolution for copy-neutral loss of heterozygosity (LOH). In addition, each SNP is represented in at least 15x redundancy to increase the signal-to-noise ratio for making accurate copy number variation (CNV) and absence of heterozygosity (AOH) calls across the genome. As few as 10 consecutive probes are necessary to make accurate CNV calls, demonstrating the high performance level of the Infinium assay. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,6 hours 15 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) Specialized Sample Types FFPE System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 4,000.00 |
| Illumina/HumanCytoSNP FFPE-12 v2.1 DNA Analysis BeadChip Kit (48 samples) 250,000 loci. Each package contains 4 BeadChip | WG-321-1004 | Illumina | 產(chǎn)品編號(hào)： WG-321-1004美 元 價(jià)： $6960.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The HumanCytoSNP FFPE-12 BeadChip interrogates >262,000 genomic Markers. The content consists of intelligently selected tag SNPs that provide comprehensive genomic coverage. With dense and even Marker spacing, the BeadChip content can also be used to precisely detect structural aberrations, allowing researchers to accurately identify structural differences between paired-normal and tumor samples. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,2 hours 10 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) Specialized Sample Types FFPE System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 6,960.00 |
| Illumina/HumanKaryomap-12 DNA Analysis Kit (24 samples)/RH-103-1001/1 Ea | RH-103-1001 | Illumina | 產(chǎn)品編號(hào)： RH-103-1001美 元 價(jià)： $3758.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The HumanKaryomap-12 DNA Analysis Kit is a comprehensive genome-wide test available at the single-cell level. It provides insight into the inheritance of single-gene defects. This BeadChip array targets ~300,000 of the most informative Markers in the genome for efficient genome-wide coverage. Karyomapping uses bioMarkers within the genome to assess the likelihood of an embryo carrying a gene variant involved in a single-gene disorder. Preimplantation genetic diagnosis (PGD) with karyomapping enables screening of embryos for the likelihood of carrying the defective gene prior to transfer to the uterus. This method uses SNP (single nucleotide polymorphisms) array technology to confirm the presence or absence of a specific allele. Specifications: Assay Time ~2 days (shortened Infinium protocol) Hands-on Time ~4 hours Input Quantity 400 ng genomic DNA from parent and reference samples + SureMDA whole-genome-amplified single cells from embryo biopsy samples Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs) System Compatibility NextSeq 550,iScan Method PGD Array Specialized Sample Types Single Cells Species Category Human | 3,758.00 |
| Illumina/SureRef Reference Male DNA (128 ?l)/PR-40-415203-00/1 Ea | PR-40-415203-00 | Illumina | 產(chǎn)品編號(hào)： PR-40-415203-00美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The SureRef Pack contains both SureRef Reference Male DNA and SureRef Reference Female DNA, each sufficient for 16 reference labeling reactions. The individual DNAs are also available separately. SureRef DNA products are matched, in terms of quality and size of DNA fragment to a single cell or a few cells. Extracted DNA should be amplified with the SurePlex DNA Amplification System and used as part of 24sure laboratory product protocols. | 0.00 |
| Illumina/SurePlex DNA Amplification System (50 reactions)/PR-40-415101-00/1 Ea | PR-40-415101-00 | Illumina | 產(chǎn)品編號(hào)： PR-40-415101-00美 元 價(jià)： $1380.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Preimplantation genetic screening (PGS) with 24sure microarrays provides a comprehensive and accurate assessment of all 24 chromosomes from an embryo biopsy. The arrays can be used to screen for aneuploidy in first and second polar bodies, blastomere biopsies, and trophectoderm biopsies. The 24sure assay is objective, ensuring a high degree of confidence in the results and subsequent selection of embryos least likely to have aneuploidy for transfer. Widely used, proven PGS – Method of choice for many of the world’s reference laboratories Fast, reliable results – Comprehensive, accurate assessment of all 24 chromosomes in 12 hours Straightforward workflow – Optimized protocols include minimal tube transfers, documented quality control (QC) stages, and flexIBLe stopping points Straightforward Workflow Is Complete in 12 Hours The straightforward 24sure protocol used standard laboratory techniques, providing a fast, accurate method for chromosome screening with minimal sensitivity to technical errors and designed to fit into existing workflows. Screening can be completed in 12 hours, and therefore does not interfere with tight schedules of a fresh IVF cycle. Specifications: Assay Time ~12 hours Hands-On Time ~2.5 hours Input Quantity Single cell or multi-cell samples Technology Microarray Specialized Sample Types Single Cells Species Category Human Variant Class Chromosomal Abnormalities,Structural Variants,Copy Number Variants (CNVs) Method PGS Array Significantly Higher Rate of Pregnancy May Be PossIBLe with PGS: The pregnancy rate shown for embryos analyzed using preimplantation genetic screening and morphology is 69.1%, much higher than the 41.7% achieved using morphology screening alone.1 Pilot study of young, good prognosis patients (age < 35, first-time IVF, no history of prior miscarriage, n = 103). PGS with 24sure Arrays Reduces the Effect of Maternal Age on Implantation and Pregnancy Rates: Although aneuploidy risk increases with maternal age, PGS using 24sure arrays on either day 3 or day 5 embryos diminishes the effect of maternal age on implantation and pregnancy rates.2 24Sure Laboratory Workflow: The 24sure laboratory workflow is a straightforward procedure that is completed in <12 hours. BlueFuse Multi Software Delivers a Complete Data Analysis and Information Management System: BlueFuse Multi Software provides a complete solution for analyzing, storing, and reporting 24sure results. A. Sample database displays experimental information. B. Array images imported directly from the scanner. C. Profiles for sample and reference chromosomes. D. Automated cycle reports. | 1,380.00 |
| Illumina/HumanCytoSNP-12 v2.1 BeadChip Kit (288 samples)/WG-320-2104/1 Ea | WG-320-2104 | Illumina | 產(chǎn)品編號(hào)： WG-320-2104美 元 價(jià)： $41760.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The 12-sample HumanCytoSNP-12 BeadChip is a powerful, whole-genome scanning panel designed for efficient, high-throughput analysis of genetic and structural variations that are most relevant to human disease. This scalable, proven solution offers substantially better resolution to detect smaller regions than fluorescence in situ hybridization (FISH) or comparative genomic hybridization (CGH).1 Complete panel of genome-wide tag single nucleotide polymorphisms (SNPs) and Markers targeting all regions of known cytogenetic importance, incorporating ~300,000 “best of the best” SNPs with the highest tagging power Average SNP call rates and reproducibility of > 99.9%, and low noise for copy number measurements Detect many types and sizes of structural variation in the human genome that affect phenotypes, including duplications, deletions, amplifications, copy-neutral loss of heterozygosity (LOH), and mosaicism Process up to 12 samples in parallel, increasing sample throughput and decreasing experimental variABIlity Process samples using the single-tube, PCR-free Infinium HD Assay that requires only 200ng DNA per sample Comprehensive data analysis with intuitive BlueFuse Multi Software streamlines copy number assessment and results reporting The HumanCytoSNP-12 BeadChip is optimized to detect cytogenetic abnormalities most relevant to human disease.1-2 Content includes ~300,000 SNPs targeting regions shown to be important for cytogenetic analysis. The result is dense coverage of ~250 disease regions, including subtelomeric regions, pericentromeric regions, and sex chromosomes, commonly screened in cytogenetics labs. Sufficient SNP coverage is provided to determine dosage sensitivity of > 800 genes. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,6 hours 15 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 41,760.00 |
| Illumina/SureMDA DNA Amplification System (96 reactions)/PR-40-405102-00/1 Ea | PR-40-405102-00 | Illumina | 產(chǎn)品編號(hào)： PR-40-405102-00美 元 價(jià)： $2920.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The HumanKaryomap-12 DNA Analysis Kit is a comprehensive genome-wide test available at the single-cell level. It provides insight into the inheritance of single-gene defects. This BeadChip array targets ~300,000 of the most informative Markers in the genome for efficient genome-wide coverage. Karyomapping uses bioMarkers within the genome to assess the likelihood of an embryo carrying a gene variant involved in a single-gene disorder. Preimplantation genetic diagnosis (PGD) with karyomapping enables screening of embryos for the likelihood of carrying the defective gene prior to transfer to the uterus. This method uses SNP (single nucleotide polymorphisms) array technology to confirm the presence or absence of a specific allele. Specifications: Assay Time ~2 days (shortened Infinium protocol) Hands-on Time ~4 hours Input Quantity 400 ng genomic DNA from parent and reference samples + SureMDA whole-genome-amplified single cells from embryo biopsy samples Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs) System Compatibility NextSeq 550,iScan Method PGD Array Specialized Sample Types Single Cells Species Category Human | 2,920.00 |
| Illumina/HumanCytoSNP-12 v2.1 BeadChip Kit (24 samples)/WG-320-2102/1 Ea | WG-320-2102 | Illumina | 產(chǎn)品編號(hào)： WG-320-2102美 元 價(jià)： $3720.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The 12-sample HumanCytoSNP-12 BeadChip is a powerful, whole-genome scanning panel designed for efficient, high-throughput analysis of genetic and structural variations that are most relevant to human disease. This scalable, proven solution offers substantially better resolution to detect smaller regions than fluorescence in situ hybridization (FISH) or comparative genomic hybridization (CGH).1 Complete panel of genome-wide tag single nucleotide polymorphisms (SNPs) and Markers targeting all regions of known cytogenetic importance, incorporating ~300,000 “best of the best” SNPs with the highest tagging power Average SNP call rates and reproducibility of > 99.9%, and low noise for copy number measurements Detect many types and sizes of structural variation in the human genome that affect phenotypes, including duplications, deletions, amplifications, copy-neutral loss of heterozygosity (LOH), and mosaicism Process up to 12 samples in parallel, increasing sample throughput and decreasing experimental variABIlity Process samples using the single-tube, PCR-free Infinium HD Assay that requires only 200ng DNA per sample Comprehensive data analysis with intuitive BlueFuse Multi Software streamlines copy number assessment and results reporting The HumanCytoSNP-12 BeadChip is optimized to detect cytogenetic abnormalities most relevant to human disease.1-2 Content includes ~300,000 SNPs targeting regions shown to be important for cytogenetic analysis. The result is dense coverage of ~250 disease regions, including subtelomeric regions, pericentromeric regions, and sex chromosomes, commonly screened in cytogenetics labs. Sufficient SNP coverage is provided to determine dosage sensitivity of > 800 genes. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,6 hours 15 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 3,720.00 |
| Illumina/TruSight Cardio Sequencing Kit for NextSeq (48 indexes, 48 samples, 4 enrichments)/FC-141-1011/1 Ea | FC-141-1011 | Illumina | 產(chǎn)品編號(hào)： FC-141-1011美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Expertly defined genes selected in collaboration with the Imperial College of London 99% of the targeted regions covered at a depth of at least 20×* Cost to sequence is ~ $1 US per gene; fully supported on Illumina sequencing and informatics platforms The TruSight Cardio Kit uses next-generation sequencing (NGS) to provide comprehensive coverage of 174 genes with known associations to 17 ICCs, including cardiomyopathies, arrhythmias, aortopathies, and more. Genes were expertly selected with researchers at the National Heart and Lung Institute at the Imperial College of London. Content includes genes known to be associated with hereditary heart disease and emerging genes found in the literature.1 Specifications: Input Quantity 50 ng DNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants Specialized Sample Types Low Input Technology Sequencing Species Category Human Method Targeted DNA Sequencing | 0.00 |
| Illumina/MiSeq® Reagent Kit v3 - PGS/RH-102-1001/1 Ea | RH-102-1001 | Illumina | 產(chǎn)品編號(hào)： RH-102-1001美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The VeriSeq PGS Kit takes advantage of next-generation sequencing (NGS) technology to provide comprehensive, accurate screening of all 24 chromosomes for selection of embryos most likely to be euploid. Preimplantation genetic screening (PGS) results generated using VeriSeq PGS are comparable to those achieved with the widely used array-based 24sure technology. In addition, NGS offers the opportunity for improved assay workflow, higher throughput, and enhanced performance.1 Industry-leADIng data quality: More than 90% of the world’s sequencing data is generated by Illumina sequencing by synthesis (SBS) chemistry* Fast, streamlined workflow: Sample to answer in approximately 12 hours High-throughput analysis: Screen up to 24 samples per run Ultra-Low Input NGS offers a highly sensitive method for screening embryos, requiring as little as 1 ng of DNA from a SurePlex DNA amplification reaction. DNA can be obtained from a blastomere biopsy, from a day 3 embryo, or from a trophectodermal (TE) biopsy from a blastocyst. *Data calculations on file. Illumina, Inc., 2015. Specifications: Assay Time 11 hours Hands-On Time 4 hours Input Quantity 30 to 300 ng depending on QC results System Compatibility MiSeq,MiSeqDx in Research Mode Method PGS Sequencing Technology Sequencing Specialized Sample Types Single Cells Species Category Human Variant Class Chromosomal Abnormalities,Structural Variants,Copy Number Variants (CNVs) | 0.00 |
| Illumina/TruSight Cardio Sequencing Kit for MiSeq and MiSeqDx (12 indexes, 12 samples, 1 enrichment)/FC-141-1010/1 Ea | FC-141-1010 | Illumina | 產(chǎn)品編號(hào)： FC-141-1010美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Expertly defined genes selected in collaboration with the Imperial College of London 99% of the targeted regions covered at a depth of at least 20×* Cost to sequence is ~ $1 US per gene; fully supported on Illumina sequencing and informatics platforms The TruSight Cardio Kit uses next-generation sequencing (NGS) to provide comprehensive coverage of 174 genes with known associations to 17 ICCs, including cardiomyopathies, arrhythmias, aortopathies, and more. Genes were expertly selected with researchers at the National Heart and Lung Institute at the Imperial College of London. Content includes genes known to be associated with hereditary heart disease and emerging genes found in the literature.1 Specifications: Input Quantity 50 ng DNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants Specialized Sample Types Low Input Technology Sequencing Species Category Human Method Targeted DNA Sequencing | 0.00 |
| Illumina/SureRef Pack (16 reference hybridizations)/PR-40-415205-PK/1 Ea | PR-40-415205-PK | Illumina | 產(chǎn)品編號(hào)： PR-40-415205-PK美 元 價(jià)： $349.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Preimplantation genetic screening (PGS) with 24sure microarrays provides a comprehensive and accurate assessment of all 24 chromosomes from an embryo biopsy. The arrays can be used to screen for aneuploidy in first and second polar bodies, blastomere biopsies, and trophectoderm biopsies. The 24sure assay is objective, ensuring a high degree of confidence in the results and subsequent selection of embryos least likely to have aneuploidy for transfer. Widely used, proven PGS – Method of choice for many of the world’s reference laboratories Fast, reliable results – Comprehensive, accurate assessment of all 24 chromosomes in 12 hours Straightforward workflow – Optimized protocols include minimal tube transfers, documented quality control (QC) stages, and flexIBLe stopping points Straightforward Workflow Is Complete in 12 Hours The straightforward 24sure protocol used standard laboratory techniques, providing a fast, accurate method for chromosome screening with minimal sensitivity to technical errors and designed to fit into existing workflows. Screening can be completed in 12 hours, and therefore does not interfere with tight schedules of a fresh IVF cycle. Specifications: Assay Time ~12 hours Hands-On Time ~2.5 hours Input Quantity Single cell or multi-cell samples Technology Microarray Specialized Sample Types Single Cells Species Category Human Variant Class Chromosomal Abnormalities,Structural Variants,Copy Number Variants (CNVs) Method PGS Array Significantly Higher Rate of Pregnancy May Be PossIBLe with PGS: The pregnancy rate shown for embryos analyzed using preimplantation genetic screening and morphology is 69.1%, much higher than the 41.7% achieved using morphology screening alone.1 Pilot study of young, good prognosis patients (age < 35, first-time IVF, no history of prior miscarriage, n = 103). PGS with 24sure Arrays Reduces the Effect of Maternal Age on Implantation and Pregnancy Rates: Although aneuploidy risk increases with maternal age, PGS using 24sure arrays on either day 3 or day 5 embryos diminishes the effect of maternal age on implantation and pregnancy rates.2 24Sure Laboratory Workflow: The 24sure laboratory workflow is a straightforward procedure that is completed in <12 hours. BlueFuse Multi Software Delivers a Complete Data Analysis and Information Management System: BlueFuse Multi Software provides a complete solution for analyzing, storing, and reporting 24sure results. A. Sample database displays experimental information. B. Array images imported directly from the scanner. C. Profiles for sample and reference chromosomes. D. Automated cycle reports. | 349.00 |
| Illumina/HumanCytoSNP-12 v2.1 BeadChip Kit (48 samples)/WG-320-2103/1 Ea | WG-320-2103 | Illumina | 產(chǎn)品編號(hào)： WG-320-2103美 元 價(jià)： $6960.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The 12-sample HumanCytoSNP-12 BeadChip is a powerful, whole-genome scanning panel designed for efficient, high-throughput analysis of genetic and structural variations that are most relevant to human disease. This scalable, proven solution offers substantially better resolution to detect smaller regions than fluorescence in situ hybridization (FISH) or comparative genomic hybridization (CGH).1 Complete panel of genome-wide tag single nucleotide polymorphisms (SNPs) and Markers targeting all regions of known cytogenetic importance, incorporating ~300,000 “best of the best” SNPs with the highest tagging power Average SNP call rates and reproducibility of > 99.9%, and low noise for copy number measurements Detect many types and sizes of structural variation in the human genome that affect phenotypes, including duplications, deletions, amplifications, copy-neutral loss of heterozygosity (LOH), and mosaicism Process up to 12 samples in parallel, increasing sample throughput and decreasing experimental variABIlity Process samples using the single-tube, PCR-free Infinium HD Assay that requires only 200ng DNA per sample Comprehensive data analysis with intuitive BlueFuse Multi Software streamlines copy number assessment and results reporting The HumanCytoSNP-12 BeadChip is optimized to detect cytogenetic abnormalities most relevant to human disease.1-2 Content includes ~300,000 SNPs targeting regions shown to be important for cytogenetic analysis. The result is dense coverage of ~250 disease regions, including subtelomeric regions, pericentromeric regions, and sex chromosomes, commonly screened in cytogenetics labs. Sufficient SNP coverage is provided to determine dosage sensitivity of > 800 genes. Specifications: Assay Time 3 days Hands-On Time 1 hour 5 min. for automated 8-beadchip workflow,6 hours 15 min. for manual 8-beadchip workflow Input Quantity 200 ng DNA Method Genome-Wide Genotyping Array,Cytogenomic Array Technology Microarray Variant Class Single Nucleotide Polymorphisms (SNPs),Loss of Heterozygosity (LOH),Chromosomal Abnormalities,Copy Number Variants (CNVs) System Compatibility NextSeq 550,iScan Species Category Human Cancer Type Hematological,Solid Tumor | 6,960.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (Bacteria) 24 reactions 99% of rRNA from Gram-negative and Gram-positive bacterial R | MRZB12424 | Illumina | 產(chǎn)品編號(hào)： MRZB12424美 元 價(jià)： $2066.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Removes ribosomal RNA (rRNA) from intact and partially degraded mixtures of Gram (+) and Gram (–) bacteria in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for small sample quantities – only 1 μg of total RNA required Virtually all rRNA is depleted from intact and partially degraded samples in 2 hours. Sequencing is an important discovery tool for research into disease, development, and more. The sequencing data from samples treated with the Ribo-Zero rRNA Removal Kit (Bacteria) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants and isoforms. This kit offers informative sequencing results by removing unwanted cytoplasmic (nuclear-encoded) rRNA from bacterial mixtures prior to sequencing. | 2,066.00 |
| Illumina/Globin-Zero Gold rRNA Removal Kit 6 reactions 99% of rRNA and >99% of globin mRNA from 1 µg - 5 µg of blood to | GZG1206 | Illumina | 產(chǎn)品編號(hào)： GZG1206美 元 價(jià)： $567.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Remove globin mRNA and ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small sample quantities – only 1 μg of total RNA required Blood is an important sample for research into thousands of rare diseases and other disorders. The sequencing data from samples treated with Globin-Zero are focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. Globin-Zero removes unwanted globin mRNA, as well as cytoplasmic and mitochondrial rRNA, from mammalian blood RNA samples before sequencing library construction. Alternative kits ScriptSeq Complete Gold Kit (Blood): Recommended for sequencing low input samples (e.g. 100 ng of total RNA) Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs Globin-Zero Gold removes globin mRNA, as well as rRNA from nuclear and mitochondrial regions: Globin-Zero Gold depletes unwanted globin mRNA and ribosomal RNA from total RNA extracted from blood. Removal of these unwanted subunits produces sequencing results that are heavily focused on BIOLOGically informative genomic regions. Globin-Zero Gold efficiently removes both globin mRNA and rRNA: Removal of these unwanted subunits allows generation of sequencing libraries that produce data heavily focused on BIOLOGically informative genetic regions. | 567.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (Gram-Positive Bacteria) 6 reactions 99% of rRNA from 1-5 µg of Gram-positive bacter | MRZGP126 | Illumina | 產(chǎn)品編號(hào)： MRZGP126美 元 價(jià)： $582.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Removes ribosomal RNA (rRNA) from intact and partially degraded Gram (+) bacteria Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for small sample quantities – only 1 μg of total RNA required Nuclear rRNA removed: 23S, 16S, 5S Sequencing is an important discovery tool for research into disease, development, and more. The sequencing data from samples treated with the Ribo-Zero rRNA Removal Kit (Gram-Positive Bacteria) are focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. The Ribo-Zero rRNA Removal Kit (Gram-Positive Bacteria) offers informative sequencing results by removing unwanted rRNA prior to sequencing. The kit removes rRNA from both intact and partially degraded samples. Removes all major rRNA subunits The Ribo-Zero rRNA Removal Kit (Gram-Positive Bacteria) depletes unwanted rRNA from total RNA. Removal of these unwanted subunits produces sequencing results that are heavily focused on BIOLOGically informative genomic regions. | 582.00 |
| Illumina/Ribo-Zero Gold rRNA Removal Kit (Epidemiology) 6 reactions/MRZE706/1 Ea | MRZE706 | Illumina | 產(chǎn)品編號(hào)： MRZE706美 元 價(jià)： $582.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Removes cytoplasmic and mitochondrial ribosomal RNA (rRNA) from samples composed of human/mouse/rat, Gram-positive and Gram-negative bacterial RNA (see table) Requires 500 ng to 2.5 μg total RNA per sample rRNA removal from both intact and partially degraded RNA Single-pass, 90- to 120-minute process Recovers all fragments of human and bacterial non-ribosomal RNAs Applicable to a broad spectrum of bacteria The Ribo-Zero Gold rRNA Removal Kit (Epidemiology) combines Ribo-Zero Gold (Human/Mouse/Rat) and Ribo-Zero (Bacteria) rRNA removal reagents into a single solution that effectively removes rRNA, including human mitochondrial RNA, from samples composed of both human/mouse/rat and bacterial RNA. Hypothesis-free NGS is more sensitive to diversity than 16S profiling Ribo-Zero Gold rRNA Removal Kit (Epidemiology) has increased sensitivity to BIOLOGical diversity because it captures all metatranscriptomic information (instead of directed capture with 16S profiling). Overview of the Ribo-Zero process Virtually all rRNA is depleted in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Related Information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs Specifications: Technology Sequencing Species Category Human,Mouse,Rat,Bacteria Specialized Sample Types FFPE System Compatibility Genome Analyzer IIx,HiSeq 2000,MiSeq,NextSeq 550,HiSeq 3000,HiSeq 1000,HiSeq 1500,NextSeq 500,HiSeq 2500,HiSeq 4000 | 582.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (Plant Leaf) 6 reactions/MRZPL116/1 Ea | MRZPL116 | Illumina | 產(chǎn)品編號(hào)： MRZPL116美 元 價(jià)： $582.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Removes cytoplasmic, mitochondrial, and chloroplast ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small sample quantities – only 1 μg of total RNA required Virtually all rRNA is depleted from intact and partially degraded samples in 2 hours. Sequencing is an important discovery tool for plant research. The sequencing data from samples treated with Ribo-Zero (Plant Leaf) and Ribo-Zero (Plant Seed/Root) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. Ribo-Zero (Plant Leaf) and Ribo-Zero (Plant Seed/Root) offer informative sequencing results by removing unwanted cytoplasmic, mitochondrial, and chloroplast rRNA prior to sequencing. In order to achieve maximum depletion of rRNA, the Ribo-Zero (Plant Leaf) kit contains a higher percentage of probes to deplete chloroplast rRNA compared to Ribo-Zero (Plant Seed/Root). Overview of the Ribo-Zero process Virtually all rRNA is depleted in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Alternative kits ScriptSeq Complete Kit (Plant): Recommended for low input plant samples (e.g. 100 ng of total RNA). Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs | 582.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (Gram-Negative Bacteria) 6 reactions 99% of rRNA from 1- 5 µg of Gram-negative bacte | MRZGN126 | Illumina | 產(chǎn)品編號(hào)： MRZGN126美 元 價(jià)： $582.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Remove ribosomal RNA (rRNA) from intact and partially degraded Gram (-) bacteria Sequencing data contain complete transcriptome of coding and noncoding RNA species Good for small sample quantities – only 1 μg of total RNA required Nuclear rRNA removed: 23S, 16S, 5S Sequencing is an important discovery tool for research into disease, development, and more. The sequencing data from samples treated with the Ribo-Zero rRNA Removal Kit (Gram-Negative Bacteria) are focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. The Ribo-Zero rRNA Removal Kit (Gram-Negative Bacteria) offers informative sequencing results by removing unwanted rRNA prior to sequencing. The kit removes rRNA from intact and partially degraded samples. Removes all major rRNA subunits The Ribo-Zero rRNA Removal Kit (Gram-Negative Bacteria) depletes unwanted rRNA from total RNA. Removal of these unwanted subunits produces sequencing results that are heavily focused on BIOLOGically informative genomic regions. | 582.00 |
| Illumina/Globin-Zero Gold rRNA Removal Kit 24 reactions 99% of rRNA and >99% of globin mRNA from 1 µg - 5 µg of blood t | GZG1224 | Illumina | 產(chǎn)品編號(hào)： GZG1224美 元 價(jià)： $2016.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Remove globin mRNA and ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small sample quantities – only 1 μg of total RNA required Blood is an important sample for research into thousands of rare diseases and other disorders. The sequencing data from samples treated with Globin-Zero are focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. Globin-Zero removes unwanted globin mRNA, as well as cytoplasmic and mitochondrial rRNA, from mammalian blood RNA samples before sequencing library construction. Alternative kits ScriptSeq Complete Gold Kit (Blood): Recommended for sequencing low input samples (e.g. 100 ng of total RNA) Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs Globin-Zero Gold removes globin mRNA, as well as rRNA from nuclear and mitochondrial regions: Globin-Zero Gold depletes unwanted globin mRNA and ribosomal RNA from total RNA extracted from blood. Removal of these unwanted subunits produces sequencing results that are heavily focused on BIOLOGically informative genomic regions. Globin-Zero Gold efficiently removes both globin mRNA and rRNA: Removal of these unwanted subunits allows generation of sequencing libraries that produce data heavily focused on BIOLOGically informative genetic regions. | 2,016.00 |
| Illumina/Ribo-Zero Gold rRNA Removal Kit (Yeast) 24 reactions/MRZY1324/1 Ea | MRZY1324 | Illumina | 產(chǎn)品編號(hào)： MRZY1324美 元 價(jià)： $2016.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Depletes ribosomal RNA (rRNA) Sequencing results contain entire transcriptome of coding and noncoding RNA species Good for intact and partially degraded small samples – only 1 μg of total RNA required The yeast transcriptome is more complex than previously thought. RNA-Seq of yeast is a valuable approach for mapping the transcriptome to characterize novel and low abundance transcripts. The Ribo-Zero Gold rRNA Removal Kit (Yeast) offers informative sequencing results by removing unwanted rRNA before sequencing. Gene coverage is enhanced following depletion by Ribo-Zero Gold (Yeast). Subsequent library construction and sequencing produces reads focused on informative genomic regions. | 2,016.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (Plant Leaf) 24 reactions 99% of nuclear-encoded and chloroplast rRNA from 1-5 µg of | MRZPL1224 | Illumina | 產(chǎn)品編號(hào)： MRZPL1224美 元 價(jià)： $2066.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Removes cytoplasmic, mitochondrial, and chloroplast ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small sample quantities – only 1 μg of total RNA required Virtually all rRNA is depleted from intact and partially degraded samples in 2 hours. Sequencing is an important discovery tool for plant research. The sequencing data from samples treated with Ribo-Zero (Plant Leaf) and Ribo-Zero (Plant Seed/Root) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. Ribo-Zero (Plant Leaf) and Ribo-Zero (Plant Seed/Root) offer informative sequencing results by removing unwanted cytoplasmic, mitochondrial, and chloroplast rRNA prior to sequencing. In order to achieve maximum depletion of rRNA, the Ribo-Zero (Plant Leaf) kit contains a higher percentage of probes to deplete chloroplast rRNA compared to Ribo-Zero (Plant Seed/Root). Overview of the Ribo-Zero process Virtually all rRNA is depleted in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Alternative kits ScriptSeq Complete Kit (Plant): Recommended for low input plant samples (e.g. 100 ng of total RNA). Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs | 2,066.00 |
| Illumina/rRNA Removal Kit (Epidemiology) 24 reactions/MRZE724/1 Ea | MRZE724 | Illumina | 產(chǎn)品編號(hào)： MRZE724美 元 價(jià)： $2066.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Removes cytoplasmic and mitochondrial ribosomal RNA (rRNA) from samples composed of human/mouse/rat, Gram-positive and Gram-negative bacterial RNA (see table) Requires 500 ng to 2.5 μg total RNA per sample rRNA removal from both intact and partially degraded RNA Single-pass, 90- to 120-minute process Recovers all fragments of human and bacterial non-ribosomal RNAs Applicable to a broad spectrum of bacteria The Ribo-Zero Gold rRNA Removal Kit (Epidemiology) combines Ribo-Zero Gold (Human/Mouse/Rat) and Ribo-Zero (Bacteria) rRNA removal reagents into a single solution that effectively removes rRNA, including human mitochondrial RNA, from samples composed of both human/mouse/rat and bacterial RNA. Hypothesis-free NGS is more sensitive to diversity than 16S profiling Ribo-Zero Gold rRNA Removal Kit (Epidemiology) has increased sensitivity to BIOLOGical diversity because it captures all metatranscriptomic information (instead of directed capture with 16S profiling). Overview of the Ribo-Zero process Virtually all rRNA is depleted in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Related Information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs Specifications: Technology Sequencing Species Category Human,Mouse,Rat,Bacteria Specialized Sample Types FFPE System Compatibility Genome Analyzer IIx,HiSeq 2000,MiSeq,NextSeq 550,HiSeq 3000,HiSeq 1000,HiSeq 1500,NextSeq 500,HiSeq 2500,HiSeq 4000 | 2,066.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (H/M/R) 6 reactions/MRZH116/1 Ea | MRZH116 | Illumina | 產(chǎn)品編號(hào)： MRZH116美 元 價(jià)： $582.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Ribo-Zero rRNA Removal Kit (Human | Product Highlights: Removes ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small samples – only 1 μg of total RNA required Sequencing is an important discovery tool for research into disease, development, and more. The sequencing data from samples treated with Ribo-Zero (Human/Mouse/Rat) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants and isoforms. Ribo-Zero (Human/Mouse/Rat) offers informative sequencing results by removing unwanted rRNA prior to sequencing. This kit removes cytoplasmic (nuclear-encoded) rRNAs. Ribo-Zero retains the complete transcriptome Ribo-Zero removes rRNA in order to retain the regulatory regions of noncoding RNA, even from low-quality samples. Other methods, such as Poly(A) depletion, do not retain noncoding, regulatory information. Overview of the Ribo-Zero process Virtually all rRNA is depleted from intact, degraded, and badly degraded (FFPE) samples in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Alternative kit versions The Ribo-Zero Gold (Human/Mouse/Rat) rRNA Removal Kit removes both cytoplasmic and mitochondrial rRNAs, and is compatIBLe with low input samples (e.g. 100 ng of total RNA). Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs | 582.00 |
| Illumina/Ribo-Zero Gold rRNA Removal Kit (H/M/R) (24 reactions) 99% of cytoplasmic and mitochondrial rRNA from human, mo | MRZG12324 | Illumina | 產(chǎn)品編號(hào)： MRZG12324美 元 價(jià)： $2066.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Ribo-Zero Gold rRNA Removal Kit (Human | Product Highlights: Removes ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small sample quantities – only 1 μg of total RNA required Sequencing is an important discovery tool for research into disease, development, and more. The sequencing data from samples treated with Ribo-Zero Gold (Human/Mouse/Rat) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. Ribo-Zero Gold (Human/Mouse/Rat) offers informative sequencing results by removing unwanted rRNA prior to sequencing. This kit removes both cytoplasmic (nuclear-encoded) and mitochondrial rRNAs. Ribo-Zero retains the complete transcriptome Ribo-Zero removes rRNA in order to retain the regulatory regions of noncoding RNA, even from low-quality samples. Other methods, such as Poly(A) depletion, do not retain noncoding, regulatory information. Overview of the Ribo-Zero process Virtually all rRNA is depleted from intact, degraded, and badly degraded (FFPE) samples in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Alternative kits Ribo-Zero rRNA Removal Kit (Human/Mouse/Rat): Removes cytoplasmic rRNA only. Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs | 2,066.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (Plant Seed/Root) 6 reactions/MRZSR116/1 Ea | MRZSR116 | Illumina | 產(chǎn)品編號(hào)： MRZSR116美 元 價(jià)： $582.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Removes cytoplasmic, mitochondrial, and chloroplast ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small sample quantities – only 1 μg of total RNA required Virtually all rRNA is depleted from intact and partially degraded samples in 2 hours. Sequencing is an important discovery tool for plant research. The sequencing data from samples treated with Ribo-Zero (Plant Leaf) and Ribo-Zero (Plant Seed/Root) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. Ribo-Zero (Plant Leaf) and Ribo-Zero (Plant Seed/Root) offer informative sequencing results by removing unwanted cytoplasmic, mitochondrial, and chloroplast rRNA prior to sequencing. In order to achieve maximum depletion of rRNA, the Ribo-Zero (Plant Leaf) kit contains a higher percentage of probes to deplete chloroplast rRNA compared to Ribo-Zero (Plant Seed/Root). Overview of the Ribo-Zero process Virtually all rRNA is depleted in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Alternative kits ScriptSeq Complete Kit (Plant): Recommended for low input plant samples (e.g. 100 ng of total RNA). Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs | 582.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (H/M/R) 24 reactions/MRZH11124/1 Ea | MRZH11124 | Illumina | 產(chǎn)品編號(hào)： MRZH11124美 元 價(jià)： $2066.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Ribo-Zero rRNA Removal Kit (Human | Product Highlights: Removes ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small samples – only 1 μg of total RNA required Sequencing is an important discovery tool for research into disease, development, and more. The sequencing data from samples treated with Ribo-Zero (Human/Mouse/Rat) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants and isoforms. Ribo-Zero (Human/Mouse/Rat) offers informative sequencing results by removing unwanted rRNA prior to sequencing. This kit removes cytoplasmic (nuclear-encoded) rRNAs. Ribo-Zero retains the complete transcriptome Ribo-Zero removes rRNA in order to retain the regulatory regions of noncoding RNA, even from low-quality samples. Other methods, such as Poly(A) depletion, do not retain noncoding, regulatory information. Overview of the Ribo-Zero process Virtually all rRNA is depleted from intact, degraded, and badly degraded (FFPE) samples in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Alternative kit versions The Ribo-Zero Gold (Human/Mouse/Rat) rRNA Removal Kit removes both cytoplasmic and mitochondrial rRNAs, and is compatIBLe with low input samples (e.g. 100 ng of total RNA). Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs | 2,066.00 |
| Illumina/Ribo-Zero Gold rRNA Removal Kit (H/M/R) (6 reactions)/MRZG126/1 Ea | MRZG126 | Illumina | 產(chǎn)品編號(hào)： MRZG126美 元 價(jià)： $582.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Ribo-Zero Gold rRNA Removal Kit (Human | Product Highlights: Removes ribosomal RNA (rRNA) in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for intact and partially degraded small sample quantities – only 1 μg of total RNA required Sequencing is an important discovery tool for research into disease, development, and more. The sequencing data from samples treated with Ribo-Zero Gold (Human/Mouse/Rat) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants, and isoforms. Ribo-Zero Gold (Human/Mouse/Rat) offers informative sequencing results by removing unwanted rRNA prior to sequencing. This kit removes both cytoplasmic (nuclear-encoded) and mitochondrial rRNAs. Ribo-Zero retains the complete transcriptome Ribo-Zero removes rRNA in order to retain the regulatory regions of noncoding RNA, even from low-quality samples. Other methods, such as Poly(A) depletion, do not retain noncoding, regulatory information. Overview of the Ribo-Zero process Virtually all rRNA is depleted from intact, degraded, and badly degraded (FFPE) samples in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Alternative kits Ribo-Zero rRNA Removal Kit (Human/Mouse/Rat): Removes cytoplasmic rRNA only. Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs Specifications: Technology Sequencing Specialized Sample Types FFPE Species Category Human,Mouse,Rat System Compatibility MiSeq,Genome Analyzer IIx,HiSeq 2000,NextSeq 550,HiSeq 3000,HiSeq 1000,HiSeq 1500,NextSeq 500,HiSeq 2500,HiSeq 4000 | 582.00 |
| Illumina/Ribo-Zero rRNA Removal Kit (Bacteria) 6 reactions/MRZMB126/1 Ea | MRZMB126 | Illumina | 產(chǎn)品編號(hào)： MRZMB126美 元 價(jià)： $582.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Removes ribosomal RNA (rRNA) from intact and partially degraded mixtures of Gram (+) and Gram (–) bacteria in a single pass Sequencing data contains complete transcriptome of coding and noncoding RNA species Good for small sample quantities – only 1 μg of total RNA required Virtually all rRNA is depleted from intact and partially degraded samples in 2 hours. Sequencing is an important discovery tool for research into disease, development, and more. The sequencing data from samples treated with the Ribo-Zero rRNA Removal Kit (Bacteria) is focused on valuable RNA species, to facilitate discovery of relevant genes, splice variants and isoforms. This kit offers informative sequencing results by removing unwanted cytoplasmic (nuclear-encoded) rRNA from bacterial mixtures prior to sequencing. Overview of the Ribo-Zero process Virtually all rRNA is depleted in 2 hours. Step 1: Wash the magnetic beads Step 2: Treat samples with rRNA Removal Solution Step 3: Remove rRNA Step 4: Purify rRNA-depleted samples, and proceed with library preparation Alternative kits ScriptSeq Complete Kit (Bacteria): Recommended for sequencing low input samples (e.g. 100 ng of total RNA). Related information rRNA Removal Kit Selection Guide Ribo-Zero Kit Species Compatibility Ribo-Zero Kit FAQs | 582.00 |
| Illumina/Ribo-Zero Gold rRNA Removal Kit (Yeast) 6 reactions/MRZY1306/1 Ea | MRZY1306 | Illumina | 產(chǎn)品編號(hào)： MRZY1306美 元 價(jià)： $567.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 分子類>核酸提取純化>RNA提取純化試劑公司分類： Molecular Biology Reagents | Product Highlights: Depletes ribosomal RNA (rRNA) Sequencing results contain entire transcriptome of coding and noncoding RNA species Good for intact and partially degraded small samples – only 1 μg of total RNA required The yeast transcriptome is more complex than previously thought. RNA-Seq of yeast is a valuable approach for mapping the transcriptome to characterize novel and low abundance transcripts. The Ribo-Zero Gold rRNA Removal Kit (Yeast) offers informative sequencing results by removing unwanted rRNA before sequencing. Gene coverage is enhanced following depletion by Ribo-Zero Gold (Yeast). Subsequent library construction and sequencing produces reads focused on informative genomic regions. | 567.00 |
| Illumina | |||||
| Illumina/Tip Depth Gauge/A1-99-102/1 Ea | A1-99-102 | Illumina | 產(chǎn)品編號(hào)： A1-99-102美 元 價(jià)： $150.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: The Tip Depth Gauge calibrates the probe depth for the Tecan Genesis Freedom EVO or Freedom EVO-2 liquid-handling robot used during automation of array-based assays such as the Infinium Assay. | 150.00 |
| Illumina/Infinium Te-Flow Thermometer Assembly/A1-99-109/1 Ea | A1-99-109 | Illumina | 產(chǎn)品編號(hào)： A1-99-109美 元 價(jià)： $680.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: The Infinium TeFlow Thermometer Assembly, which includes the Thermometer and a temperature probe, reads the temperature in the TeFlow rack during Infinium Whole-Genome Genotyping Assays and Infinium HD Assays. | 680.00 |
| Illumina/Infinium Multi-Sample Alignment Fixture (1)/WG-15-310/1 Ea | WG-15-310 | Illumina | 產(chǎn)品編號(hào)： WG-15-310美 元 價(jià)： $650.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: The Infinium Alignment Fixture allows correct assembly of the TeFlow Chamber, HD or LCG BeadChip array, and spacer to ensure optimal processing during the Infinium Assay. | 650.00 |
| 以下是已發(fā)布的 上面都是未發(fā)到化工網(wǎng) 綠圖 黑圖 桔圖 | Illumina | ||||
| Illumina/cBot 2 Barcoded Strip Tubes (8 well)/20005160/1 Ea | 20005160 | Illumina | 產(chǎn)品編號(hào)： 20005160美 元 價(jià)： $500.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: The cBot 2 barcoded 8-well strip tube enables sample tracking though the sequencing workflow. The keyed strip tube minimizes sample mix-ups by single orientation loADIng and a unique barcode that is read by an onboard barcode scanner on the cBot 2 System. Each strip tube has two barcodes enabling sample tracking on liquid handling robots and the cBot 2 System. Each strip tube box contains 100 strip tubes. This item is an accessory for the cBot 2 System, which automates cluster generation on HiSeq sequencing systems. Specifications: Technology Sequencing System Compatibility HiSeq 4000,HiSeq X Ten,HiScanSQ,HiSeq 3000,HiSeq X Five,HiSeq 2500 | 500.00 |
| Illumina/Infinium MIDI Heatblock Insert/BD-60-601/1 Ea | BD-60-601 | Illumina | 產(chǎn)品編號(hào)： BD-60-601美 元 價(jià)： $160.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | 160.00 | |
| Illumina/Infinium BeadChip Glass Tray (1)/BD-60-460/1 Ea | BD-60-460 | Illumina | 產(chǎn)品編號(hào)： BD-60-460美 元 價(jià)： $62.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: The BeadChip Wash Rack and Glass Tray (purchased separately) are used to handle BeadChip arrays following hybridization during Direct Hybridization and Infinium Assays. | 62.00 |
| Illumina/Infinium Hybridization Chamber Inserts (8)/WG-15-301/1 Ea | WG-15-301 | Illumina | 產(chǎn)品編號(hào)： WG-15-301美 元 價(jià)： $1200.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | 1,200.00 | |
| Illumina/Infinium Hybridization Chamber Inserts (8)/WG-15-301/1 Ea | WG-15-301 | Illumina | 產(chǎn)品編號(hào)： WG-15-301美 元 價(jià)： $1200.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: The Infinium Hybridization Chambers are used for BeadChip array hybridization during Infinium Assays. Each Infinium Hybridization Chamber processes four Infinium BeadChip arrays per day. A gasket fits inside the chamber to ensure proper BeadChip retention and optimal exposure to reagents. One gasket is included in the package, and replacement gaskets are available for purchase separately. | 1,200.00 |
| Illumina/Replacement Infinium Hybridization Chamber Gasket (1)/BD-60-403/1 Ea | BD-60-403 | Illumina | 產(chǎn)品編號(hào)： BD-60-403美 元 價(jià)： $7.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: The Infinium Hybridization Chambers are used for BeadChip array hybridization during Infinium Assays. Each Infinium Hybridization Chamber processes four Infinium BeadChip arrays per day. A gasket fits inside the chamber to ensure proper BeadChip retention and optimal exposure to reagents. One gasket is included in the package, and replacement gaskets are available for purchase separately. | 7.00 |
| Illumina/Infinium Hybridization Chamber (1)/BD-60-402/1 Ea | BD-60-402 | Illumina | 產(chǎn)品編號(hào)： BD-60-402美 元 價(jià)： $840.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: The Infinium Hybridization Chambers are used for BeadChip array hybridization during Infinium Assays. Each Infinium Hybridization Chamber processes four Infinium BeadChip arrays per day. A gasket fits inside the chamber to ensure proper BeadChip retention and optimal exposure to reagents. One gasket is included in the package, and replacement gaskets are available for purchase separately. | 840.00 |
| Illumina/Infinium BeadChip Boxes (10)/BD-60-500/1 Ea | BD-60-500 | Illumina | 產(chǎn)品編號(hào)： BD-60-500美 元 價(jià)： $40.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: Store BeadChips used in Illumina array-based assays. Each BeadChip storage box holds 25 BeadChips. | 40.00 |
| Illumina/Infinium BeadChip Expansion Package/WG-10-201/1 Ea | WG-10-201 | Illumina | 產(chǎn)品編號(hào)： WG-10-201美 元 價(jià)： $7000.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: Store BeadChips used in Illumina array-based assays. Each BeadChip storage box holds 25 BeadChips. | 7,000.00 |
| Illumina/Teflon-coated replacement probes for Tecan Robot (1)/A1-99-101/1 Ea | A1-99-101 | Illumina | 產(chǎn)品編號(hào)： A1-99-101美 元 價(jià)： $70.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>配件>常用設(shè)備公司分類： Accessory Products | Product Highlights: Store BeadChips used in Illumina array-based assays. Each BeadChip storage box holds 25 BeadChips. | 70.00 |
| Illumina | |||||
| Illumina/MiSeqDx Cystic Fibrosis 139-Variant Assay (20 runs, 960 samples)/DX-102-1003/1 Ea | DX-102-1003 | Illumina | 產(chǎn)品編號(hào)： DX-102-1003美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>臨床研究公司分類： In Vitro Diagnostic (IVD) Products | Product Highlights: Compared to the current ACMG recommended cystic fibrosis variant panel, the MiSeqDx Cystic Fibrosis 139-Variant Assay offers: Improved Detection Rates of Cystic Fibrosis-Causing Variants Detection of couples at risk increased from 72% to ~91%1 Reduced Additional Testing Highly accurate and reproducIBLe sequencing technology delivers dependable results The MiSeqDx Cystic Fibrosis 139-Variant Assay is an FDA-cleared in vitro diagnostic (IVD) next-generation sequencing test designed to detect 139 CFTR variants as defined in the CFTR2 database. Other methods test only for those variants most commonly found in Caucasians, potentially missing CF-causing variants across broader ethnic groups. The MiSeqDx Cystic Fibrosis 139-Variant Assay offers the largest CF variant panel to overcome this bias and provide comprehensive detection across diverse demographics.2 Widely adopted next-generation sequencing The MiSeqDx Cystic Fibrosis 139-Variant Assay provides a fully integrated molecular CF testing solution on the MiSeqDx instrument. Simply prepare libraries from 250 ng gDNA, load on to the MiSeqDx for sequencing using Illumina sequencing by synthesis (SBS) chemistry, and analyze with the user-friendly software. The automated workflow is quick and easy to perform, potentially minimizing human error. A complete kit for library preparation and sequencing The MiSeqDx Cystic Fibrosis 139-Variant Assay includes all index primers and reagents needed for library preparation, sample multiplexing, and sequencing in a single kit. MiSeqDx sequencing reagents are packaged in a convenient ready-to-use format, minimizing hands-on time and increasing uniformity in all tests. To accommodate a broad spectrum of testing needs, from small to large volumes, the assay is available in two kit configurations (2 or 20 runs). Specifications: Assay Time 2.5 days Hands-On Time 3.5 hours Input Quantity 250 ng genomic DNA System Compatibility MiSeqDx Technology Sequencing | 0.00 |
| Illumina/MiSeqDx Universal Kit (2 runs, up to 96 samples)/DX-103-1001/1 Ea | DX-103-1001 | Illumina | 產(chǎn)品編號(hào)： DX-103-1001美 元 價(jià)： $12410.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>臨床研究公司分類： In Vitro Diagnostic (IVD) Products | Product Highlights: FlexIBLe Assay Design - Develop assays to meet the specific needs of your customers Validated Kit – Verified performance standards for supplied library preparation and sequencing reagents Fast Results - Go from genomic DNA to fully analyzed data in < 2 days High Assay Reproducibility - Consistent results between multiple operators and systems The MiSeqDx Universal Kit is a validated, FDA-cleared amplicon sequencing solution that enables clinical laboratories to develop their own next-generation sequencing (NGS) assays for use on the FDA-cleared MiSeqDx instrument. Together, the MiSeqDx Universal Kit and instrument offer molecular diagnostics labs the accuracy and reliABIlity needed to bring NGS capABIlities into their facilities. Customized assay design With the MiSeqDx Universal Kit, molecular diagnostics labs develop assays using oligonucleotide probes they have designed on their own. This provides users with the flexibility to target specific regions of interest and better meet the needs of their customers. Streamlined workflow Prepare libraries, load on to the MiSeqDx for sequencing using the Illumina sequencing by synthesis (SBS) chemistry, and analyze with the user-friendly software. The automated workflow is quick and easy to perform, potentially minimizing human error. Specifications: Assay Time 1 day Hands-On Time 2.5 hours Input Quantity 250 ng genomic DNA System Compatibility MiSeqDx Technology Sequencing | 12,410.00 |
| Illumina/MiSeqDx Cystic Fibrosis Clinical Sequencing Assay (6 runs, 48 samples)/DX-102-1001/1 Ea | DX-102-1001 | Illumina | 產(chǎn)品編號(hào)： DX-102-1001美 元 價(jià)： $9504.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>臨床研究公司分類： In Vitro Diagnostic (IVD) Products | Product Highlights: Complete View of the CFTR Gene Capture all variants in the protein coding regions and intron/exon boundaries of the CFTR gene Accurate Results Deep coverage (> 3,000×) allows detection accuracy with a Positive Agreement (PA) of 99.66%* No Demographic Bias Sequencing the CFTR gene removes the bias inherent in existing genotyping panels1 * PA includes polyTG/polyT variants The MiSeqDx Cystic Fibrosis Clinical Sequencing Assay is the first FDA-cleared in vitro diagnostic (IVD) next-generation sequencing (NGS) test designed to sequence all protein coding regions and intron/exon boundaries of the CFTR gene, including two large deletions, two deep intronic mutations, and indels in homopolymeric regions such as the 2184delA deletion. The assay also automatically detects polyTG/polyT variants. Viewing the CFTR sequence eliminates any bias inherent in existing cystic fibrosis (CF) panels. As a result, the MiSeqDx Cystic Fibrosis Clinical Sequencing Assay can uncover rare mutations not accounted for in standard tests. Widely adopted next-generation sequencing The MiSeqDx Cystic Fibrosis Clinical Sequencing Assay provides a fully integrated molecular CF testing solution on the MiSeqDx instrument. Amplify 27 CFTR gene target regions in a single PCR step, and multiplex samples to streamline your workflow. Simply prepare libraries from 250 ng gDNA, load on to the MiSeqDx for sequencing using the Illumina sequencing by synthesis (SBS) chemistry, and analyze with the user-friendly software. A complete kit for library preparation and sequencing The MiSeqDx Cystic Fibrosis Clinical Sequencing Assay includes all index primers and reagents needed for library preparation, sample multiplexing, and sequencing in a single kit. MiSeqDx sequencing reagents are packaged in a convenient ready-to-use format, minimizing hands-on time, and increasing uniformity in all tests. Specifications: Assay Time 2.5 days Hands-On Time 3.5 hours Input Quantity 250 ng genomic DNA System Compatibility MiSeqDx Technology Sequencing | |
| Illumina/MiSeqDx Cystic Fibrosis 139-Variant Assay (2 runs, 96 samples)/DX-102-1004/1 Ea | DX-102-1004 | Illumina | 產(chǎn)品編號(hào)： DX-102-1004美 元 價(jià)： $5760.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>臨床研究公司分類： In Vitro Diagnostic (IVD) Products | Product Highlights: Compared to the current ACMG recommended cystic fibrosis variant panel, the MiSeqDx Cystic Fibrosis 139-Variant Assay offers: Improved Detection Rates of Cystic Fibrosis-Causing Variants Detection of couples at risk increased from 72% to ~91%1 Reduced Additional Testing Highly accurate and reproducIBLe sequencing technology delivers dependable results The MiSeqDx Cystic Fibrosis 139-Variant Assay is an FDA-cleared in vitro diagnostic (IVD) next-generation sequencing test designed to detect 139 CFTR variants as defined in the CFTR2 database. Other methods test only for those variants most commonly found in Caucasians, potentially missing CF-causing variants across broader ethnic groups. The MiSeqDx Cystic Fibrosis 139-Variant Assay offers the largest CF variant panel to overcome this bias and provide comprehensive detection across diverse demographics.2 Widely adopted next-generation sequencing The MiSeqDx Cystic Fibrosis 139-Variant Assay provides a fully integrated molecular CF testing solution on the MiSeqDx instrument. Simply prepare libraries from 250 ng gDNA, load on to the MiSeqDx for sequencing using Illumina sequencing by synthesis (SBS) chemistry, and analyze with the user-friendly software. The automated workflow is quick and easy to perform, potentially minimizing human error. A complete kit for library preparation and sequencing The MiSeqDx Cystic Fibrosis 139-Variant Assay includes all index primers and reagents needed for library preparation, sample multiplexing, and sequencing in a single kit. MiSeqDx sequencing reagents are packaged in a convenient ready-to-use format, minimizing hands-on time and increasing uniformity in all tests. To accommodate a broad spectrum of testing needs, from small to large volumes, the assay is available in two kit configurations (2 or 20 runs). Specifications: Assay Time 2.5 days Hands-On Time 3.5 hours Input Quantity 250 ng genomic DNA System Compatibility MiSeqDx Technology Sequencing | 5,760.00 |
| 以下未發(fā)布 | Illumina | ||||
| Illumina/TruSight RNA Fusion Panel Set A (48 samples)/RS-304-1002/1 Ea | RS-304-1002 | Illumina | 產(chǎn)品編號(hào)： RS-304-1002美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: This targeted RNA sequencing panel is a cost-effective solution to detect gene fusions in multiple cancer types, regardless of origin. Covering 507 fusion-associated genes, a single assay enables researchers to assess most known cancer-related fusions in blood, bone marrow, and FFPE samples, with the power to identify novel fusion gene partners. Industry-validated content for a comprehensive view of cancer-related fusion genes, detecting common and novel fusions From RNA to results in 4 days including on-instrument software that displays fusion calls Compatibility with desktop sequencers to maximize lab budgets Optimized RNA sequencing for all sample types, including FFPE tissues Simple Fusion Report for Customers New to NGS On-instrument fusion calling provides NGS-based fusion detection to labs without additional bioinformatics support. The analysis provides a list of detected fusions, relevant disease associations (as identified by the Mitelman database), and evidence of fusion-supporting reads. Robust, ReproducIBLe, and Low-Input Fusion Assay This assay accommodates as little input as 20 ng FFPE RNA or 10 ng fresh-frozen total RNA. The TruSight RNA Fusion Panel provides a sensitive, reproducIBLe, and economical solution for studies of gene fusions in cancer research. Specifications: Assay Time 2.5 days Hands-On Time 11 hours Input Quantity 10 ng total RNA, 20–100 ng FFPE RNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Method Targeted RNA Sequencing,Sequencing for Cytogenomics Variant Class Gene Fusions Specialized Sample Types FFPE,Low Input Technology Sequencing Species Category Human Cancer Type Pan-Cancer | 0.00 |
| Illumina/TruSight Rapid Capture (4 indexes, 16 samples, 4 enrichments)/FC-140-1103/1 Ea | FC-140-1103 | Illumina | 產(chǎn)品編號(hào)： FC-140-1103美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Targeting genes previously linked to a predisposition towards cancer. Developed in collaboration with Professor Nazneen Rahman and team at the Institute of Cancer Research (ICR), London Targets 94 genes and 284 SNPs associated with a predisposition towards cancer TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources. The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatIBLe with TruSight Rapid Capture. TruSight Cancer Sample Datasets 6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project * Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 1.5 days Input Quantity 50 ng System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Specialized Sample Types Low Input Technology Sequencing Species Category Human Variant Class Germline Variants Cancer Type Pan-Cancer Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight HLA v2 Sequencing Panel (24 samples, automated)/20005170/1 Ea | 20005170 | Illumina | 產(chǎn)品編號(hào)： 20005170美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The TruSight HLA v2 Sequencing Panel provides clinical researchers with a broad-coverage, ultra-high–resolution human leukocyte antigen (HLA) typing solution for simple, rapid assessment of the HLA region in a single assay. It features: High-resolution sequencing of 11 HLA loci Workflow with library preparation, sequencing and data analysis/reporting Accurate and high-resolution HLA typing for unambiguous results Capture Full HLA Gene Sequences TruSight HLA v2 covers all commonly typed HLA loci, plus those with emerging relevance. This panel enables sequencing of Class I HLA-A, B, and C; Class II HLA-DRB1/3/4/5, HLA-DQA1, HLA-DQB1, HLA-DPA1, and HLA-DPB1. This expands coverage beyond the classic loci, with full gene coverage, enabling discovery of new alleles without the need to design new primers. Sample-to-Report Workflow with Optimized Data Analysis The comprehensive solution includes reagents and software optimized for HLA analysis. A simplified workflow enables turnaround time of less than 48 hours and increased efficiency with less than 4.5 hours of hands-on time. On-instrument software analyzes sequence data; TruSight HLA Assign Software provides flexIBLe options for post-analysis reporting of results. High-Accuracy HLA Typing The expanded coverage of TruSight HLA v2 provides high resolution, eliminating the need for follow-up testing to obtain a confident typing result. View HLA Loci. How TruSight HLA v2 Works TruSight HLA v2 amplifies HLA loci with long-range PCR. After amplification, Nextera tagmentation fragments the DNA and leaves behind a sequence tag. An additional PCR then adds sequence adapters and indexing primers to generate sequencing-ready DNA libraries. Prepared libraries are then loaded directly onto a MiniSeq, MiSeq or NextSeq System for sequencing. Analysis Software Highlights The Assign 2.0 TruSight HLA analysis software assists with the assignment of a human leukocyte antigen (HLA) type. The software is designed to analyze data from libraries prepared with Illumina TruSight HLA Sequencing Panels and then sequenced on an Illumina sequencer. Use Assign 2.0 to import sequence data, perform base calling, edit sequences, and compare a sample consensus sequence with the IMGT/HLA database of alleles. Specifications: Assay Time 48 hours Hands-On Time 4.5 hours Input Quantity 400 ng DNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Variant Class Single Nucleotide Polymorphisms (SNPs) Technology Sequencing Species Category Human Method HLA Sequencing | 0.00 |
| Illumina/TruSight Tumor 170 Kit plus Watson for Genomics/20018622/1 Ea | 20018622 | Illumina | 產(chǎn)品編號(hào)： 20018622美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight Tumor 170, a next-generation sequencing assay designed to cover 170 genes associated with common solid tumors, is an enrichment-based targeted panel that simultaneously analyzes DNA and RNA, covering a wide range of genes and variant types. The comprehensive nature provides laboratories with a deep view into the genetics of cancer. Comprehensive Coverage of Cancer-Related Variants Assessment of fusions, splice variants, insertions/deletions and single-nucleotide variants (SNVs), and amplifications in one assay using DNA and RNA creates efficiencies in sample usage, time, and cost. Accurate Results from Low-Quality Samples1 Variant detection with as little as 40 ng DNA and RNA input, and as low as 5% mutant allele frequency, maximizes the results from precious formalin-fixed paraffin-embedded (FFPE) samples. Integrated, Streamlined Workflow DNA and RNA are prepared in parallel with an integrated workflow following DNA shearing/CDNA synthesis. Specifications: Assay Time ~2 days (Library Prep) Hands-On Time ~10.5 hours Input Quantity 40 ng DNA and/or RNA Method Targeted RNA Sequencing,Targeted DNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Somatic Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE,Low Input System Compatibility NextSeq 550,NextSeq 500,HiSeq 2500 Technology Sequencing Species Category Human Cancer Type Solid Tumor Scientific Posters: AACR 2017: TruSight Tumor 170 and Tumor Mutational Burden Results of analysis indicate that TruSight Tumor 170, with comprehensive coverage of cancer-related genes, shows high concordance with whole exome sequencing for accurate assessment of tumor mutational burden. Learn More AACR 2017: TruSight Tumor 170 and Solid Tumor Profiling Analytical Performance with FFPE Samples Standard extractions from FFPE embedded samples provide sufficient material (40ng) in >95% of samples that were extracted by Illumina. This data shows that the TruSight Tumor 170 panel is a robust assay that generates passing sample QC data in >85% of samples with varying quality, and in >95% of samples that have quality metrics that fall within the recommendations for the kit. Learn More AACR 2017: TruSight Tumor 170 for Small Nucleotide Variations and Gene Amplifications in FFPE DNA Samples TruSight Tumor 170 can achieve high sensitivity and specificity for the detection of somatic variants (small variants and CNVs) from DNA extracted from FFPE tissues. Learn More AACR 2017: TruSight Tumor 170 for Fusions and Splice Variants in FFPE RNA Tumor Samples Through examining limit of detection in the context of RNA expression, this study shows that TruSight Tumor 170 provides high sensitivity and specificity in RNA variant calling down to 5 copies of transcript per ng of input. Learn More | 0.00 |
| Illumina/TruSight Rapid Capture (24 indexes, 48 samples, 4 enrichments)/FC-140-1104/1 Ea | FC-140-1104 | Illumina | 產(chǎn)品編號(hào)： FC-140-1104美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Targeting genes previously linked to a predisposition towards cancer. Developed in collaboration with Professor Nazneen Rahman and team at the Institute of Cancer Research (ICR), London Targets 94 genes and 284 SNPs associated with a predisposition towards cancer TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources. The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatIBLe with TruSight Rapid Capture. TruSight Cancer Sample Datasets 6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project * Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 1.5 days Input Quantity 50 ng System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Specialized Sample Types Low Input Technology Sequencing Species Category Human Variant Class Germline Variants Cancer Type Pan-Cancer Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight One Expanded Sequencing Panel (36 samples)/FC-141-2007/1 Ea | FC-141-2007 | Illumina | 產(chǎn)品編號(hào)： FC-141-2007美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight One Sequencing Panels enable labs to expand and streamline their sequencing portfolio, while managing costs. Two panels offer options to target up to 6700 genes associated with human disease, with high coverage Single assay includes multiple genes of interest, replacing iterative testing Easy, flexIBLe gene filtering and annotation options simplify BIOLOGical interpretation and reporting These panels provide clinical research labs with an affordable solution for managing a diverse assay portfolio. The TruSight One Sequencing Panel provides comprehensive coverage of > 4800 disease-associated genes, while the TruSight One Expanded Sequencing Panel targets ~1900 additional genes with recent disease associations in the scientific literature. Investigators can choose to analyze all of the genes on the panel or focus on a specific subset. With a single assay, labs can expand existing menus, streamline workflows, or create an entire portfolio of sequencing options. Specifications: Input Quantity 50 ng Content Specifications ~12 Mb genomic content for TruSight One; ~16.5 Mb genomic content for TruSight One Expanded Multiplexing Up to 96-plex System Compatibility MiSeq,NextSeq 550,HiSeq 3000,MiSeqDx in Research Mode,MiniSeq,NextSeq 500,HiSeq 2500,NovaSeq 6000,HiSeq 4000 Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants Specialized Sample Types Low Input Technology Sequencing Species Category Human Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight Rapid Capture (24 indexes, 96 samples, 8 enrichments)/FC-140-1105/1 Ea | FC-140-1105 | Illumina | 產(chǎn)品編號(hào)： FC-140-1105美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Targeting genes previously linked to a predisposition towards cancer. Developed in collaboration with Professor Nazneen Rahman and team at the Institute of Cancer Research (ICR), London Targets 94 genes and 284 SNPs associated with a predisposition towards cancer TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources. The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatIBLe with TruSight Rapid Capture. TruSight Cancer Sample Datasets 6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project * Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 1.5 days Input Quantity 50 ng System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Specialized Sample Types Low Input Technology Sequencing Species Category Human Variant Class Germline Variants Cancer Type Pan-Cancer Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight RNA Pan-Cancer Panel Set B/RS-303-1003/1 Ea | RS-303-1003 | Illumina | 產(chǎn)品編號(hào)： RS-303-1003美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The TruSight RNA Pan-Cancer panel provides a comprehensive analysis of the cancer transcriptome. It offers: Gene expression information, variant calling, and fusion detection with known and novel gene fusion partners Optimized, low-input protocol for a wide range of sample types including FFPE A comprehensive view of cancer pathways Economical RNA sequencing (RNA-Seq) on a desktop sequencer Highly Sensitive and Economical Targeted Sequencing The TruSight RNA Pan-Cancer panel enables the quantitative measurement of gene expression as well as the detection of gene fusions with both known and novel gene fusion partners. The panel accommodates as little as 10 ng of total RNA input (or 20 ng from FFPE samples). The focus on a subset of relevant genes enables RNA-Seq with high sensitivity at 8 samples per run on a desktop sequencer, allowing cost-effective access to NGS for any lab. Intuitive Cloud-based Data Analysis Analysis can be performed using the RNA-Seq Alignment BaseSpace App. This intuitive tool performs fusion calling andvariant detection, and provides gene expression profiles, offering a comprehensive solution to all cancer researchers. TruSight RNA Pan-Cancer Sample Datasets MiSeq Data 10 ng of human reference RNA (UHR), human reference brain RNA (Brain), cell line RNA (MCF7), and 20 ng of breast tumor FFPE RNA (BT) were prepared using the TruSight RNA Pan-Cancer Panel and sequenced on the MiSeq System. Read mapping and fusion calling were performed using the RNA-Seq Alignment App with STAR aligner on BaseSpace Sequence Hub. View Project MiniSeq Data Human reference RNA (HBRR and UHRR), cell line RNA (MCF7), and breast tumor RNA samples were prepared using the TruSight RNA Pan-Cancer panel, and 8 samples were sequenced on the MiniSeq System at a 2x76bp read length with single indexing. The total yield was 4.2 Gb with 96.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project Access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 2.5 days Hands-On Time 11 hours Input Quantity 10 ng total RNA,20 - 100 ng FFPE RNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Method Targeted RNA Sequencing,Sequencing for Cytogenomics Variant Class Gene Fusions,Somatic Variants,Novel Transcripts,Transcript Variants Specialized Sample Types FFPE,Low Input Technology Sequencing Species Category Human Cancer Type Pan-Cancer | 0.00 |
| Illumina/TruSight HLA v2 Sequencing Panel (24 samples)/20000215/1 Ea | 20000215 | Illumina | 產(chǎn)品編號(hào)： 20000215美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The TruSight HLA v2 Sequencing Panel provides clinical researchers with a broad-coverage, ultra-high–resolution human leukocyte antigen (HLA) typing solution for simple, rapid assessment of the HLA region in a single assay. It features: High-resolution sequencing of 11 HLA loci Workflow with library preparation, sequencing and data analysis/reporting Accurate and high-resolution HLA typing for unambiguous results Capture Full HLA Gene Sequences TruSight HLA v2 covers all commonly typed HLA loci, plus those with emerging relevance. This panel enables sequencing of Class I HLA-A, B, and C; Class II HLA-DRB1/3/4/5, HLA-DQA1, HLA-DQB1, HLA-DPA1, and HLA-DPB1. This expands coverage beyond the classic loci, with full gene coverage, enabling discovery of new alleles without the need to design new primers. Sample-to-Report Workflow with Optimized Data Analysis The comprehensive solution includes reagents and software optimized for HLA analysis. A simplified workflow enables turnaround time of less than 48 hours and increased efficiency with less than 4.5 hours of hands-on time. On-instrument software analyzes sequence data; TruSight HLA Assign Software provides flexIBLe options for post-analysis reporting of results. High-Accuracy HLA Typing The expanded coverage of TruSight HLA v2 provides high resolution, eliminating the need for follow-up testing to obtain a confident typing result. View HLA Loci. How TruSight HLA v2 Works TruSight HLA v2 amplifies HLA loci with long-range PCR. After amplification, Nextera tagmentation fragments the DNA and leaves behind a sequence tag. An additional PCR then adds sequence adapters and indexing primers to generate sequencing-ready DNA libraries. Prepared libraries are then loaded directly onto a MiniSeq, MiSeq or NextSeq System for sequencing. Analysis Software Highlights The Assign 2.0 TruSight HLA analysis software assists with the assignment of a human leukocyte antigen (HLA) type. The software is designed to analyze data from libraries prepared with Illumina TruSight HLA Sequencing Panels and then sequenced on an Illumina sequencer. Use Assign 2.0 to import sequence data, perform base calling, edit sequences, and compare a sample consensus sequence with the IMGT/HLA database of alleles. Specifications: Assay Time 48 hours Hands-On Time 4.5 hours Input Quantity 400 ng DNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Variant Class Single Nucleotide Polymorphisms (SNPs) Technology Sequencing Species Category Human Method HLA Sequencing | 0.00 |
| Illumina/TruSight Tumor 15 MiniSeq Kit/20005610/1 Ea | 20005610 | Illumina | 產(chǎn)品編號(hào)： 20005610美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight Tumor 15 uses next-generation sequencing (NGS) technology to provide a comprehensive assessment of 15 genes that are commonly mutated in solid tumors. It accurately detects low-frequency variants from 20 ng of starting DNA and is optimized for formalin-fixed, paraffin-embedded (FFPE) tumor tissue. View the Gene List Featuring a rapid workflow that can be easily integrated into lab procedures, this panel offers a single assay for accurate, economical, and rapid analysis of solid tumors. This TruSight Tumor panel offers: Comprehensive workflow: Assess 15 genes with one simple workflow instead of single, iterative gene testing with polymerase chain reaction (PCR) Efficient: Rapid turnaround with only 3.5 hours of hands-on time, going from DNA to data in approximately 36 hours Relevant gene content for solid tumors: Somatic variants selected from relevant industry guidelines1,2, key opinion leaders3,4, and pharmaceutical research Sensitive variant detection from low DNA input: Accurate somatic variant detection of 5% allele frequency using 20 ng DNA from FFPE tissue samples TruSight Tumor 15 Sample Datasets 3 human reference samples and 5 FFPE-exacted DNA samples from lung, colon, melanoma, and breast tumors were prepared using TruSight Tumor 15. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 150 bp read length configuration with dual indexing. The total yield was 7.6 Gb with 94.9% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project Access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 7 hours Hands-On Time 3.5 hours Input Quantity 20 ng System Compatibility MiSeq,MiSeqDx in Research Mode,MiniSeq Specialized Sample Types FFPE,Low Input Technology Sequencing Variant Class Somatic Variants,Insertions-Deletions (indels) Species Category Human Cancer Type Solid Tumor Method Amplicon Sequencing,Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight RNA Pan-Cancer Set A MiniSeq Kit/20005611/1 Ea | 20005611 | Illumina | 產(chǎn)品編號(hào)： 20005611美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The TruSight RNA Pan-Cancer panel provides a comprehensive analysis of the cancer transcriptome. It offers: Gene expression information, variant calling, and fusion detection with known and novel gene fusion partners Optimized, low-input protocol for a wide range of sample types including FFPE A comprehensive view of cancer pathways Economical RNA sequencing (RNA-Seq) on a desktop sequencer Highly Sensitive and Economical Targeted Sequencing The TruSight RNA Pan-Cancer panel enables the quantitative measurement of gene expression as well as the detection of gene fusions with both known and novel gene fusion partners. The panel accommodates as little as 10 ng of total RNA input (or 20 ng from FFPE samples). The focus on a subset of relevant genes enables RNA-Seq with high sensitivity at 8 samples per run on a desktop sequencer, allowing cost-effective access to NGS for any lab. Intuitive Cloud-based Data Analysis Analysis can be performed using the RNA-Seq Alignment BaseSpace App. This intuitive tool performs fusion calling andvariant detection, and provides gene expression profiles, offering a comprehensive solution to all cancer researchers. TruSight RNA Pan-Cancer Sample Datasets MiSeq Data 10 ng of human reference RNA (UHR), human reference brain RNA (Brain), cell line RNA (MCF7), and 20 ng of breast tumor FFPE RNA (BT) were prepared using the TruSight RNA Pan-Cancer Panel and sequenced on the MiSeq System. Read mapping and fusion calling were performed using the RNA-Seq Alignment App with STAR aligner on BaseSpace Sequence Hub. View Project MiniSeq Data Human reference RNA (HBRR and UHRR), cell line RNA (MCF7), and breast tumor RNA samples were prepared using the TruSight RNA Pan-Cancer panel, and 8 samples were sequenced on the MiniSeq System at a 2x76bp read length with single indexing. The total yield was 4.2 Gb with 96.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project Access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 2.5 days Hands-On Time 11 hours Input Quantity 10 ng total RNA,20 - 100 ng FFPE RNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Method Targeted RNA Sequencing,Sequencing for Cytogenomics Variant Class Gene Fusions,Somatic Variants,Novel Transcripts,Transcript Variants Specialized Sample Types FFPE,Low Input Technology Sequencing Species Category Human Cancer Type Pan-Cancer | 0.00 |
| Illumina/TG TruSight Inherited Disease Sequencing Panel (48 Samples)/TG-141-1005/1 Ea | TG-141-1005 | Illumina | 產(chǎn)品編號(hào)： TG-141-1005美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Developed in collaboration with Dr. Stephen Kingsmore and team during his tenure at Children's Mercy Hospital (CMH) for Pediatric Genomic Medicine, Dr. Carol Saunders at CMH, and Dr. Hilger Ropers at the Max Planck Institute Targets 552 genes, including coding exons, intron-exon boundaries, and regions known to harbor pathogenic mutations TruSight Inherited Disease was initially based on a 448 disease panel designed for preconception carrier testing for severe, recessive childhood diseases published by Dr. Kingsmore and team in Science Translational Medicine1. The original content was revised by Dr. Saunders, FACMG, at CMH (following ACMG guidelines for testing ultra-rare genetic diseases) to reflect the needs of medical geneticists with a primary focus on severe recessive diseases with childhood onset. Intellectual disABIlity genes were added by Dr. Ropers. The TruSight Inherited Disease sequencing panel set includes custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. Specifications: Input Quantity 50 ng DNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500,HiSeq 2500 Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants Specialized Sample Types Low Input Technology Sequencing Species Category Human Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSeq Index Plate Fixture Kit (2 fixtures)/FC-130-1005/1 Ea | FC-130-1005 | Illumina | 產(chǎn)品編號(hào)： FC-130-1005美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The TruSight HLA v2 Sequencing Panel provides clinical researchers with a broad-coverage, ultra-high–resolution human leukocyte antigen (HLA) typing solution for simple, rapid assessment of the HLA region in a single assay. It features: High-resolution sequencing of 11 HLA loci Workflow with library preparation, sequencing and data analysis/reporting Accurate and high-resolution HLA typing for unambiguous results Capture Full HLA Gene Sequences TruSight HLA v2 covers all commonly typed HLA loci, plus those with emerging relevance. This panel enables sequencing of Class I HLA-A, B, and C; Class II HLA-DRB1/3/4/5, HLA-DQA1, HLA-DQB1, HLA-DPA1, and HLA-DPB1. This expands coverage beyond the classic loci, with full gene coverage, enabling discovery of new alleles without the need to design new primers. Sample-to-Report Workflow with Optimized Data Analysis The comprehensive solution includes reagents and software optimized for HLA analysis. A simplified workflow enables turnaround time of less than 48 hours and increased efficiency with less than 4.5 hours of hands-on time. On-instrument software analyzes sequence data; TruSight HLA Assign Software provides flexIBLe options for post-analysis reporting of results. High-Accuracy HLA Typing The expanded coverage of TruSight HLA v2 provides high resolution, eliminating the need for follow-up testing to obtain a confident typing result. View HLA Loci. How TruSight HLA v2 Works TruSight HLA v2 amplifies HLA loci with long-range PCR. After amplification, Nextera tagmentation fragments the DNA and leaves behind a sequence tag. An additional PCR then adds sequence adapters and indexing primers to generate sequencing-ready DNA libraries. Prepared libraries are then loaded directly onto a MiniSeq, MiSeq or NextSeq System for sequencing. Analysis Software Highlights The Assign 2.0 TruSight HLA analysis software assists with the assignment of a human leukocyte antigen (HLA) type. The software is designed to analyze data from libraries prepared with Illumina TruSight HLA Sequencing Panels and then sequenced on an Illumina sequencer. Use Assign 2.0 to import sequence data, perform base calling, edit sequences, and compare a sample consensus sequence with the IMGT/HLA database of alleles. Specifications: Assay Time 48 hours Hands-On Time 4.5 hours Input Quantity 400 ng DNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Variant Class Single Nucleotide Polymorphisms (SNPs) Technology Sequencing Species Category Human Method HLA Sequencing | 0.00 |
| Illumina/TruSight Tumor 170 Kit (24 Samples)/OP-101-1004/1 Ea | OP-101-100 | Illumina | 產(chǎn)品編號(hào)： OP-101-1004美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight Tumor 170, a next-generation sequencing assay designed to cover 170 genes associated with common solid tumors, is an enrichment-based targeted panel that simultaneously analyzes DNA and RNA, covering a wide range of genes and variant types. The comprehensive nature provides laboratories with a deep view into the genetics of cancer. Comprehensive Coverage of Cancer-Related Variants Assessment of fusions, splice variants, insertions/deletions and single-nucleotide variants (SNVs), and amplifications in one assay using DNA and RNA creates efficiencies in sample usage, time, and cost. Accurate Results from Low-Quality Samples1 Variant detection with as little as 40 ng DNA and RNA input, and as low as 5% mutant allele frequency, maximizes the results from precious formalin-fixed paraffin-embedded (FFPE) samples. Integrated, Streamlined Workflow DNA and RNA are prepared in parallel with an integrated workflow following DNA shearing/CDNA synthesis. Specifications: Assay Time ~2 days (Library Prep) Hands-On Time ~10.5 hours Input Quantity 40 ng DNA and/or RNA Method Targeted RNA Sequencing,Targeted DNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Somatic Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE,Low Input System Compatibility NextSeq 550,NextSeq 500,HiSeq 2500 Technology Sequencing Species Category Human Cancer Type Solid Tumor Scientific Posters: AACR 2017: TruSight Tumor 170 and Tumor Mutational Burden Results of analysis indicate that TruSight Tumor 170, with comprehensive coverage of cancer-related genes, shows high concordance with whole exome sequencing for accurate assessment of tumor mutational burden. Learn More AACR 2017: TruSight Tumor 170 and Solid Tumor Profiling Analytical Performance with FFPE Samples Standard extractions from FFPE embedded samples provide sufficient material (40ng) in >95% of samples that were extracted by Illumina. This data shows that the TruSight Tumor 170 panel is a robust assay that generates passing sample QC data in >85% of samples with varying quality, and in >95% of samples that have quality metrics that fall within the recommendations for the kit. Learn More AACR 2017: TruSight Tumor 170 for Small Nucleotide Variations and Gene Amplifications in FFPE DNA Samples TruSight Tumor 170 can achieve high sensitivity and specificity for the detection of somatic variants (small variants and CNVs) from DNA extracted from FFPE tissues. Learn More AACR 2017: TruSight Tumor 170 for Fusions and Splice Variants in FFPE RNA Tumor Samples Through examining limit of detection in the context of RNA expression, this study shows that TruSight Tumor 170 provides high sensitivity and specificity in RNA variant calling down to 5 copies of transcript per ng of input. Learn More | 0.00 |
| Illumina/TruSight Rapid Capture (1 index, 8 samples, 8 enrichments)/FC-140-1101/1 Ea | FC-140-1101 | Illumina | 產(chǎn)品編號(hào)： FC-140-1101美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Targeting genes previously linked to a predisposition towards cancer. Developed in collaboration with Professor Nazneen Rahman and team at the Institute of Cancer Research (ICR), London Targets 94 genes and 284 SNPs associated with a predisposition towards cancer TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources. The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatIBLe with TruSight Rapid Capture. TruSight Cancer Sample Datasets 6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project * Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 1.5 days Input Quantity 50 ng System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Specialized Sample Types Low Input Technology Sequencing Species Category Human Variant Class Germline Variants Cancer Type Pan-Cancer Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight Tumor 26/FC-130-2001/1 Ea | FC-130-2001 | Illumina | 產(chǎn)品編號(hào)： FC-130-2001美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight Tumor 26 takes a deeper view of variation in solid tumors including lung, colon, melanoma, gastric and ovarian. This enables clinical researchers to identify low-frequency variation across 26 genes for a more comprehensive view of somatic variation. Highly accurate variant analysis at limit of detection below 5% variant allele frequency across 174 amplicons, with 1000x minimum coverage of each region Exceptional sample success rates with minimal DNA input for accurate base calling, even in degraded FFPE samples Coverage of complete exons for analysis of molecular heterogeneity in highly relevant content selected from CAP1 and NCCN2 guidelines, and late stage clinical trials3 This panel provides amplicon-based library preparation reagents, DNA QC, sample indexes, and oligos targeting identified regions of interest. Genes in TruSight Tumor 26 See which solid tumor-related genes are represented in TruSight Tumor 26. View Gene List Specifications: Assay Time 11 hours Hands-On Time 4 hours Input Quantity 30 to 300 ng depending on QC results System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Specialized Sample Types FFPE Technology Sequencing Variant Class Somatic Variants,Insertions-Deletions (indels) Species Category Human Cancer Type Solid Tumor Method Amplicon Sequencing,Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight Tumor 170 Kit, For Use with NextSeq (24 Samples)/OP-101-1003/1 Ea | OP-101-1003 | Illumina | 產(chǎn)品編號(hào)： OP-101-1003美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight Tumor 170, a next-generation sequencing assay designed to cover 170 genes associated with common solid tumors, is an enrichment-based targeted panel that simultaneously analyzes DNA and RNA, covering a wide range of genes and variant types. The comprehensive nature provides laboratories with a deep view into the genetics of cancer. Comprehensive Coverage of Cancer-Related Variants Assessment of fusions, splice variants, insertions/deletions and single-nucleotide variants (SNVs), and amplifications in one assay using DNA and RNA creates efficiencies in sample usage, time, and cost. Accurate Results from Low-Quality Samples1 Variant detection with as little as 40 ng DNA and RNA input, and as low as 5% mutant allele frequency, maximizes the results from precious formalin-fixed paraffin-embedded (FFPE) samples. Integrated, Streamlined Workflow DNA and RNA are prepared in parallel with an integrated workflow following DNA shearing/CDNA synthesis. Specifications: Assay Time ~2 days (Library Prep) Hands-On Time ~10.5 hours Input Quantity 40 ng DNA and/or RNA Method Targeted RNA Sequencing,Targeted DNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Somatic Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE,Low Input System Compatibility NextSeq 550,NextSeq 500,HiSeq 2500 Technology Sequencing Species Category Human Cancer Type Solid Tumor Scientific Posters: AACR 2017: TruSight Tumor 170 and Tumor Mutational Burden Results of analysis indicate that TruSight Tumor 170, with comprehensive coverage of cancer-related genes, shows high concordance with whole exome sequencing for accurate assessment of tumor mutational burden. Learn More AACR 2017: TruSight Tumor 170 and Solid Tumor Profiling Analytical Performance with FFPE Samples Standard extractions from FFPE embedded samples provide sufficient material (40ng) in >95% of samples that were extracted by Illumina. This data shows that the TruSight Tumor 170 panel is a robust assay that generates passing sample QC data in >85% of samples with varying quality, and in >95% of samples that have quality metrics that fall within the recommendations for the kit. Learn More AACR 2017: TruSight Tumor 170 for Small Nucleotide Variations and Gene Amplifications in FFPE DNA Samples TruSight Tumor 170 can achieve high sensitivity and specificity for the detection of somatic variants (small variants and CNVs) from DNA extracted from FFPE tissues. Learn More AACR 2017: TruSight Tumor 170 for Fusions and Splice Variants in FFPE RNA Tumor Samples Through examining limit of detection in the context of RNA expression, this study shows that TruSight Tumor 170 provides high sensitivity and specificity in RNA variant calling down to 5 copies of transcript per ng of input. Learn More | 0.00 |
| Illumina/TruSight Myeloid Sequencing Panel (96 samples)/FC-130-1010/1 Ea | FC-130-1010 | Illumina | 產(chǎn)品編號(hào)： FC-130-1010美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The TruSight Myeloid Sequencing Panel uses expert-defined content and proven next-generation sequencing (NGS) technology to identify somatic variants in myeloid malignancies. The panel content was designed by a consortium of recognized experts in blood cancer disorders and targets genes frequently mutated in: Acute myeloid leukemia (AML) Myelodysplastic syndrome (MDS) Myeloproliferative neoplasms (MPN) Chronic myelogenous leukemia (CML) Chronic myelomonocytic leukemia (CMML) Juvenile myelomonocytic leukemia (JMML) The TruSight Myeloid Sequencing Panel covers 15 full genes (exons only) and 39 additional genes where oncogenic hotspots are covered, providing a comprehensive assessment of the key genes known to be involved in myeloid malignancies in a single test. The result is an accurate, cost-effective solution that enables researchers to profile liquid tumors. View the gene list TruSight Myeloid libraries are ideally suited to run on a desktop sequencer and perform alignment and variant calling with the MiSeq Reporter or Local Run Manager Amplicon workflow with Somatic Variant Caller. Filtering and annotation can then be performed using the following Illumina annotation and filtering tools: BaseSpace Variant Interpreter or VariantStudio. Specifications: Assay Time 8 hours Hands-On Time 3 hours Input Quantity 50 ng System Compatibility MiSeq,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Technology Sequencing Variant Class Somatic Variants,Insertions-Deletions (indels) Species Category Human Cancer Type Hematological Method Amplicon Sequencing,Targeted DNA Sequencing | 0.00 |
| Illumina/TruSeq Amplicon - Cancer Panel (96 samples)/FC-130-1008/1 Ea | FC-130-1008 | Illumina | 產(chǎn)品編號(hào)： FC-130-1008美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The TruSeq Amplicon - Cancer Panel enables highly sensitive mutation detection studies of important cancer-related genes, including BRAF, KRAS, and EGFR. Mutations in these genes are linked to many cancers, including melanoma, colorectal, ovarian, and lung cancer. This cancer sequencing panel provides: A streamlined workflow including an integrated quality control assay for formalin-fixed, paraffin-embedded (FFPE) DNA Simple sample normalization Automated cluster generation and paired-end sequencing On-instrument data analysis The unique ABIlity of this assay to screen precious FFPE samples for these important variants will unlock a wealth of genomic information for many tumor types. Genes in the TruSeq Amplicon - Cancer Panel See which cancer-related genes are represented in this panel. View Gene List Specifications: Assay Time 8 hours Hands-On Time 3.5 hours Input Quantity 150 ng high-quality genomic DNA,250 ng FFPE genomic DNA System Compatibility MiSeq,MiSeqDx in Research Mode,MiniSeq Specialized Sample Types FFPE Technology Sequencing Variant Class Somatic Variants,Insertions-Deletions (indels) Species Category Human Cancer Type Pan-Cancer Method Amplicon Sequencing,Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight Rapid Capture (2 indexes, 8 samples, 4 enrichments)/FC-140-1102/1 Ea | FC-140-1102 | Illumina | 產(chǎn)品編號(hào)： FC-140-1102美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Targeting genes previously linked to a predisposition towards cancer. Developed in collaboration with Professor Nazneen Rahman and team at the Institute of Cancer Research (ICR), London Targets 94 genes and 284 SNPs associated with a predisposition towards cancer TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources. The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatIBLe with TruSight Rapid Capture. TruSight Cancer Sample Datasets 6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project * Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 1.5 days Input Quantity 50 ng System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Specialized Sample Types Low Input Technology Sequencing Species Category Human Variant Class Germline Variants Cancer Type Pan-Cancer Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight Tumor 170 Kit, For Use with NextSeq plus Watson for Genomics/20018621/1 Ea | 20018621 | Illumina | 產(chǎn)品編號(hào)： 20018621美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight Tumor 170, a next-generation sequencing assay designed to cover 170 genes associated with common solid tumors, is an enrichment-based targeted panel that simultaneously analyzes DNA and RNA, covering a wide range of genes and variant types. The comprehensive nature provides laboratories with a deep view into the genetics of cancer. Comprehensive Coverage of Cancer-Related Variants Assessment of fusions, splice variants, insertions/deletions and single-nucleotide variants (SNVs), and amplifications in one assay using DNA and RNA creates efficiencies in sample usage, time, and cost. Accurate Results from Low-Quality Samples1 Variant detection with as little as 40 ng DNA and RNA input, and as low as 5% mutant allele frequency, maximizes the results from precious formalin-fixed paraffin-embedded (FFPE) samples. Integrated, Streamlined Workflow DNA and RNA are prepared in parallel with an integrated workflow following DNA shearing/CDNA synthesis. Specifications: Assay Time ~2 days (Library Prep) Hands-On Time ~10.5 hours Input Quantity 40 ng DNA and/or RNA Method Targeted RNA Sequencing,Targeted DNA Sequencing Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Somatic Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs) Specialized Sample Types FFPE,Low Input System Compatibility NextSeq 550,NextSeq 500,HiSeq 2500 Technology Sequencing Species Category Human Cancer Type Solid Tumor Scientific Posters: AACR 2017: TruSight Tumor 170 and Tumor Mutational Burden Results of analysis indicate that TruSight Tumor 170, with comprehensive coverage of cancer-related genes, shows high concordance with whole exome sequencing for accurate assessment of tumor mutational burden. Learn More AACR 2017: TruSight Tumor 170 and Solid Tumor Profiling Analytical Performance with FFPE Samples Standard extractions from FFPE embedded samples provide sufficient material (40ng) in >95% of samples that were extracted by Illumina. This data shows that the TruSight Tumor 170 panel is a robust assay that generates passing sample QC data in >85% of samples with varying quality, and in >95% of samples that have quality metrics that fall within the recommendations for the kit. Learn More AACR 2017: TruSight Tumor 170 for Small Nucleotide Variations and Gene Amplifications in FFPE DNA Samples TruSight Tumor 170 can achieve high sensitivity and specificity for the detection of somatic variants (small variants and CNVs) from DNA extracted from FFPE tissues. Learn More AACR 2017: TruSight Tumor 170 for Fusions and Splice Variants in FFPE RNA Tumor Samples Through examining limit of detection in the context of RNA expression, this study shows that TruSight Tumor 170 provides high sensitivity and specificity in RNA variant calling down to 5 copies of transcript per ng of input. Learn More | 0.00 |
| Illumina/TruSight RNA Pan-Cancer Panel Set A/RS-303-1002/1 Ea | RS-303-1002 | Illumina | 產(chǎn)品編號(hào)： RS-303-1002美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: The TruSight RNA Pan-Cancer panel provides a comprehensive analysis of the cancer transcriptome. It offers: Gene expression information, variant calling, and fusion detection with known and novel gene fusion partners Optimized, low-input protocol for a wide range of sample types including FFPE A comprehensive view of cancer pathways Economical RNA sequencing (RNA-Seq) on a desktop sequencer Highly Sensitive and Economical Targeted Sequencing The TruSight RNA Pan-Cancer panel enables the quantitative measurement of gene expression as well as the detection of gene fusions with both known and novel gene fusion partners. The panel accommodates as little as 10 ng of total RNA input (or 20 ng from FFPE samples). The focus on a subset of relevant genes enables RNA-Seq with high sensitivity at 8 samples per run on a desktop sequencer, allowing cost-effective access to NGS for any lab. Intuitive Cloud-based Data Analysis Analysis can be performed using the RNA-Seq Alignment BaseSpace App. This intuitive tool performs fusion calling andvariant detection, and provides gene expression profiles, offering a comprehensive solution to all cancer researchers. TruSight RNA Pan-Cancer Sample Datasets MiSeq Data 10 ng of human reference RNA (UHR), human reference brain RNA (Brain), cell line RNA (MCF7), and 20 ng of breast tumor FFPE RNA (BT) were prepared using the TruSight RNA Pan-Cancer Panel and sequenced on the MiSeq System. Read mapping and fusion calling were performed using the RNA-Seq Alignment App with STAR aligner on BaseSpace Sequence Hub. View Project MiniSeq Data Human reference RNA (HBRR and UHRR), cell line RNA (MCF7), and breast tumor RNA samples were prepared using the TruSight RNA Pan-Cancer panel, and 8 samples were sequenced on the MiniSeq System at a 2x76bp read length with single indexing. The total yield was 4.2 Gb with 96.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project Access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 2.5 days Hands-On Time 11 hours Input Quantity 10 ng total RNA,20 - 100 ng FFPE RNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Method Targeted RNA Sequencing,Sequencing for Cytogenomics Variant Class Gene Fusions,Somatic Variants,Novel Transcripts,Transcript Variants Specialized Sample Types FFPE,Low Input Technology Sequencing Species Category Human Cancer Type Pan-Cancer | 0.00 |
| Illumina/TruSight Inherited Disease Sequencing Panel (48 samples)/FC-121-0205/1 Ea | FC-121-0205 | Illumina | 產(chǎn)品編號(hào)： FC-121-0205美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Developed in collaboration with Dr. Stephen Kingsmore and team during his tenure at Children's Mercy Hospital (CMH) for Pediatric Genomic Medicine, Dr. Carol Saunders at CMH, and Dr. Hilger Ropers at the Max Planck Institute Targets 552 genes, including coding exons, intron-exon boundaries, and regions known to harbor pathogenic mutations TruSight Inherited Disease was initially based on a 448 disease panel designed for preconception carrier testing for severe, recessive childhood diseases published by Dr. Kingsmore and team in Science Translational Medicine1. The original content was revised by Dr. Saunders, FACMG, at CMH (following ACMG guidelines for testing ultra-rare genetic diseases) to reflect the needs of medical geneticists with a primary focus on severe recessive diseases with childhood onset. Intellectual disABIlity genes were added by Dr. Ropers. The TruSight Inherited Disease sequencing panel set includes custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. Specifications: Input Quantity 50 ng DNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500,HiSeq 2500 Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants Specialized Sample Types Low Input Technology Sequencing Species Category Human Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight Tumor 15 (Library Prep Only)/OP-101-1002/1 Ea | OP-101-1002 | Illumina | 產(chǎn)品編號(hào)： OP-101-1002美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight Tumor 15 uses next-generation sequencing (NGS) technology to provide a comprehensive assessment of 15 genes that are commonly mutated in solid tumors. It accurately detects low-frequency variants from 20 ng of starting DNA and is optimized for formalin-fixed, paraffin-embedded (FFPE) tumor tissue. View the Gene List Featuring a rapid workflow that can be easily integrated into lab procedures, this panel offers a single assay for accurate, economical, and rapid analysis of solid tumors. This TruSight Tumor panel offers: Comprehensive workflow: Assess 15 genes with one simple workflow instead of single, iterative gene testing with polymerase chain reaction (PCR) Efficient: Rapid turnaround with only 3.5 hours of hands-on time, going from DNA to data in approximately 36 hours Relevant gene content for solid tumors: Somatic variants selected from relevant industry guidelines1,2, key opinion leaders3,4, and pharmaceutical research Sensitive variant detection from low DNA input: Accurate somatic variant detection of 5% allele frequency using 20 ng DNA from FFPE tissue samples TruSight Tumor 15 Sample Datasets 3 human reference samples and 5 FFPE-exacted DNA samples from lung, colon, melanoma, and breast tumors were prepared using TruSight Tumor 15. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 150 bp read length configuration with dual indexing. The total yield was 7.6 Gb with 94.9% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project Access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 7 hours Hands-On Time 3.5 hours Input Quantity 20 ng System Compatibility MiSeq,MiSeqDx in Research Mode,MiniSeq Specialized Sample Types FFPE,Low Input Technology Sequencing Variant Class Somatic Variants,Insertions-Deletions (indels) Species Category Human Cancer Type Solid Tumor Method Amplicon Sequencing,Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight RNA Fusion Panel Set B (48 samples)/RS-304-1003/1 Ea | RS-304-1003 | Illumina | 產(chǎn)品編號(hào)： RS-304-1003美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: This targeted RNA sequencing panel is a cost-effective solution to detect gene fusions in multiple cancer types, regardless of origin. Covering 507 fusion-associated genes, a single assay enables researchers to assess most known cancer-related fusions in blood, bone marrow, and FFPE samples, with the power to identify novel fusion gene partners. Industry-validated content for a comprehensive view of cancer-related fusion genes, detecting common and novel fusions From RNA to results in 4 days including on-instrument software that displays fusion calls Compatibility with desktop sequencers to maximize lab budgets Optimized RNA sequencing for all sample types, including FFPE tissues Simple Fusion Report for Customers New to NGS On-instrument fusion calling provides NGS-based fusion detection to labs without additional bioinformatics support. The analysis provides a list of detected fusions, relevant disease associations (as identified by the Mitelman database), and evidence of fusion-supporting reads. Robust, ReproducIBLe, and Low-Input Fusion Assay This assay accommodates as little input as 20 ng FFPE RNA or 10 ng fresh-frozen total RNA. The TruSight RNA Fusion Panel provides a sensitive, reproducIBLe, and economical solution for studies of gene fusions in cancer research. Specifications: Assay Time 2.5 days Hands-On Time 11 hours Input Quantity 10 ng total RNA, 20–100 ng FFPE RNA System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Method Targeted RNA Sequencing,Sequencing for Cytogenomics Variant Class Gene Fusions Specialized Sample Types FFPE,Low Input Technology Sequencing Species Category Human Cancer Type Pan-Cancer | 0.00 |
| Illumina/TruSight Tumor 15 MiSeq Kit/OP-101-1001/1 Ea | OP-101-1001 | Illumina | 產(chǎn)品編號(hào)： OP-101-1001美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight Tumor 15 uses next-generation sequencing (NGS) technology to provide a comprehensive assessment of 15 genes that are commonly mutated in solid tumors. It accurately detects low-frequency variants from 20 ng of starting DNA and is optimized for formalin-fixed, paraffin-embedded (FFPE) tumor tissue. View the Gene List Featuring a rapid workflow that can be easily integrated into lab procedures, this panel offers a single assay for accurate, economical, and rapid analysis of solid tumors. This TruSight Tumor panel offers: Comprehensive workflow: Assess 15 genes with one simple workflow instead of single, iterative gene testing with polymerase chain reaction (PCR) Efficient: Rapid turnaround with only 3.5 hours of hands-on time, going from DNA to data in approximately 36 hours Relevant gene content for solid tumors: Somatic variants selected from relevant industry guidelines1,2, key opinion leaders3,4, and pharmaceutical research Sensitive variant detection from low DNA input: Accurate somatic variant detection of 5% allele frequency using 20 ng DNA from FFPE tissue samples TruSight Tumor 15 Sample Datasets 3 human reference samples and 5 FFPE-exacted DNA samples from lung, colon, melanoma, and breast tumors were prepared using TruSight Tumor 15. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 150 bp read length configuration with dual indexing. The total yield was 7.6 Gb with 94.9% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project Access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 7 hours Hands-On Time 3.5 hours Input Quantity 20 ng System Compatibility MiSeq,MiSeqDx in Research Mode,MiniSeq Specialized Sample Types FFPE,Low Input Technology Sequencing Variant Class Somatic Variants,Insertions-Deletions (indels) Species Category Human Cancer Type Solid Tumor Method Amplicon Sequencing,Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight Cancer MiniSeq Kit/20005612/1 Ea | 20005612 | Illumina | 產(chǎn)品編號(hào)： 20005612美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Targeting genes previously linked to a predisposition towards cancer. Developed in collaboration with Professor Nazneen Rahman and team at the Institute of Cancer Research (ICR), London Targets 94 genes and 284 SNPs associated with a predisposition towards cancer TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources. The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatIBLe with TruSight Rapid Capture. TruSight Cancer Sample Datasets 6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project * Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 1.5 days Input Quantity 50 ng System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Specialized Sample Types Low Input Technology Sequencing Species Category Human Variant Class Germline Variants Cancer Type Pan-Cancer Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight Rapid Capture (96 indexes, 288 samples, 24 enrichments)/FC-140-1106/1 Ea | FC-140-1106 | Illumina | 產(chǎn)品編號(hào)： FC-140-1106美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: Targeting genes previously linked to a predisposition towards cancer. Developed in collaboration with Professor Nazneen Rahman and team at the Institute of Cancer Research (ICR), London Targets 94 genes and 284 SNPs associated with a predisposition towards cancer TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources. The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatIBLe with TruSight Rapid Capture. TruSight Cancer Sample Datasets 6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30. Browse the data in BaseSpace Sequence Hub: View Run View Project * Note that access to this data requires a BaseSpace Sequence Hub login. Register for BaseSpace Sequence Hub Specifications: Assay Time 1.5 days Input Quantity 50 ng System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500 Specialized Sample Types Low Input Technology Sequencing Species Category Human Variant Class Germline Variants Cancer Type Pan-Cancer Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight One Sequencing Kit (9 samples)/FC-141-1006/1 Ea | FC-141-1006 | Illumina | 產(chǎn)品編號(hào)： FC-141-1006美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight One Sequencing Panels enable labs to expand and streamline their sequencing portfolio, while managing costs. Two panels offer options to target up to 6700 genes associated with human disease, with high coverage Single assay includes multiple genes of interest, replacing iterative testing Easy, flexIBLe gene filtering and annotation options simplify BIOLOGical interpretation and reporting These panels provide clinical research labs with an affordable solution for managing a diverse assay portfolio. The TruSight One Sequencing Panel provides comprehensive coverage of > 4800 disease-associated genes, while the TruSight One Expanded Sequencing Panel targets ~1900 additional genes with recent disease associations in the scientific literature. Investigators can choose to analyze all of the genes on the panel or focus on a specific subset. With a single assay, labs can expand existing menus, streamline workflows, or create an entire portfolio of sequencing options. Specifications: Input Quantity 50 ng Content Specifications ~12 Mb genomic content for TruSight One; ~16.5 Mb genomic content for TruSight One Expanded Multiplexing Up to 96-plex System Compatibility MiSeq,NextSeq 550,HiSeq 3000,MiSeqDx in Research Mode,MiniSeq,NextSeq 500,HiSeq 2500,NovaSeq 6000,HiSeq 4000 Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants Specialized Sample Types Low Input Technology Sequencing Species Category Human Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSight One Sequencing Panel (36 samples)/FC-141-1007/1 Ea | FC-141-1007 | Illumina | 產(chǎn)品編號(hào)： FC-141-1007美 元 價(jià)： $0.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.產(chǎn)品分類： 其它>其它試劑>芯片公司分類： Clinical Research Products | Product Highlights: TruSight One Sequencing Panels enable labs to expand and streamline their sequencing portfolio, while managing costs. Two panels offer options to target up to 6700 genes associated with human disease, with high coverage Single assay includes multiple genes of interest, replacing iterative testing Easy, flexIBLe gene filtering and annotation options simplify BIOLOGical interpretation and reporting These panels provide clinical research labs with an affordable solution for managing a diverse assay portfolio. The TruSight One Sequencing Panel provides comprehensive coverage of > 4800 disease-associated genes, while the TruSight One Expanded Sequencing Panel targets ~1900 additional genes with recent disease associations in the scientific literature. Investigators can choose to analyze all of the genes on the panel or focus on a specific subset. With a single assay, labs can expand existing menus, streamline workflows, or create an entire portfolio of sequencing options. Specifications: Input Quantity 50 ng Content Specifications ~12 Mb genomic content for TruSight One; ~16.5 Mb genomic content for TruSight One Expanded Multiplexing Up to 96-plex System Compatibility MiSeq,NextSeq 550,HiSeq 3000,MiSeqDx in Research Mode,MiniSeq,NextSeq 500,HiSeq 2500,NovaSeq 6000,HiSeq 4000 Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants Specialized Sample Types Low Input Technology Sequencing Species Category Human Method Targeted DNA Sequencing | 0.00 |
| Illumina/TruSeq Stranded mRNA Library Prep Kit High Throughput (96 samples, 96 indexes)/RS-122-2103/1 Ea | RS-122-2103 | Illumina | 產(chǎn)品編號(hào)： RS-122-2103美 元 價(jià)： $4700.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: The TruSeq Stranded mRNA Library Prep Kit offers a streamlined, cost-efficient, and scalable solution for coding transcriptome analysis. It is compatIBLe with a wide range of samples. Precise and Accurate Get precise measurement of mRNA strand orientation for detection of antisense transcription, enhanced transcript annotation, and increased alignment efficiency. High coverage uniformity enhances the discovery of features such as alternative transcripts, gene fusions, and allele-specific expression. Cost-Efficient Stranded information identifies from which of the 2 DNA strands a given RNA transcript was derived. This information provides increased confidence in transcript annotation, particularly for nonhuman samples. Identifying strand origin increases the percentage of reads that align, reducing sequencing costs per sample. Scalable The kit enables robust interrogation of both standard and low-quality samples, and workflows compatIBLe with a wide range of study designs. Find an up-to-date list of high-throughput automation vendors with robotic systems compatIBLe with this library preparation kit Specifications: Assay Time ~10.5 hours Hands-On Time ~4.5 hours Input Quantity 0.1 – 1 ug total RNA or 10 - 100 ng previously isolated mRNA (from species with polyA tails) Content Specifications Captures the coding transcriptome with strand information Mechanism of Action Oligo-dT beads capture polyA tails System Compatibility NovaSeq 5000,Genome Analyzer IIx,HiSeq 2000,MiSeq,NextSeq 550,HiSeq 3000,HiSeq 1000,HiSeq 1500,NextSeq 500,HiSeq 2500,NovaSeq 6000,HiSeq 4000 Species Category Other,Mammalian,Bovine,Mouse,Human,Rat Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Novel Transcripts,Transcript Variants Technology Sequencing Method mRNA Sequencing Automation CapABIlity Liquid Handling Robots | 4,700.00 |
| Illumina/Nextera Rapid Capture Exome (8 rxn x 12 plex)/FC-140-1003/1 Ea | FC-140-1003 | Illumina | 產(chǎn)品編號(hào)： FC-140-1003美 元 價(jià)： $10290.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: The Nextera Rapid Capture Exome and Expanded Exome are all-in-one kits for library preparation and exome enrichment that allow researchers to identify coding variants up to 70% faster than other methods. This optimized exome delivers 45 Mb of expertly selected exonic content and requires as little as 4 Gb of sequencing. Extend coverage to UTRs and miRNA with Expanded Exome Nextera Rapid Capture Expanded Exome delivers 62 Mb of genomic content, including exons, untranslated regions (UTRs), and miRNA. This kit features a highly optimized probe set that delivers comprehensive coverage of exonic sequence. Illumina provides example data sets to demonstrate the high uniformity and accuracy of the Nextera Rapid Capture Exome library prep kit. View the exome sequencing data. Add on custom content to make Nextera Rapid Capture Exome even more powerful Researchers can define custom content for this workflow using Nextera Rapid Capture Custom Enrichment. This custom assay allows researchers to rapidly interrogate those portions of the human genome most important to their specific research. Choose from a fully custom design or start from a defined content set, such as Nextera Rapid Capture Exome, and include areas of interest using add-on functionality. Learn More. Find an up-to-date list of high-throughput automation vendors with robotic systems compatIBLe with this library preparation kit Specifications: Assay Time 5 hours total assay time Hands-On Time 4 hours Input Quantity 1 ug DNA (compatIBLe with most large DNA genomes) Mechanism of Action Mechanical fragmentation Multiplexing Up to 96 dual-index combinations with HT (high-throughput) kit Variant Class Small Insertions-Deletions (indels) System Compatibility HiSeq 2000,NextSeq 550,HiSeq 3000,NextSeq 500,HiSeq 2500,HiSeq 4000 Specialized Sample Types Low Input Technology Sequencing Species Category Human Automation CapABIlity Liquid Handling Robots Method Exome Sequencing | 10,290.00 |
| Illumina/20-pack MiSeq Reagent Kit v2 (300-cycles)/MS-102-2022/1 Ea | MS-102-2022 | Illumina | 產(chǎn)品編號(hào)： MS-102-2022美 元 價(jià)： $19900.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.簇生成和測(cè)序試劑公司分類： Cluster Generation & Sequencing Reagents | Product Highlights: MiSeq Reagent Kits v2 enable more output to simplify each MiSeq run. MiSeq Reagent Kits v2 retain the same pre-filled, ready-to-use reagent cartridges as the v1 kits, but offer improved chemistry to increase cluster density, decrease cycle time, and improve quality (Q) scores. MiSeq Reagent Kits v2 are also available in micro and nano formats for low output applications. Get faster cycle times, longer reads and more output from improved chemistry Dual surface imaging enables twice the number of reads compared to single surface imaging with the v1 kit Extend your read lengths with the 500-cycle kit Choose the perfect number of cycles for your application (50, 300, or 500) When coupled with the MiSeq System upgrade, the MiSeq Reagent Kits v2 allow dual surface imaging to double the amount of readable space per flow cell. MiSeq Regent Kits v2 are available in a 500-cycle format for long read lengths, as well as in the popular 50-cycle and 300-cycle formats. MiSeq Reagent Kits v2 are available in standard, micro, and nano configurations, enabling alignment to specific project requirements and scalable levels of output. View product configurations All MiSeq reagent components are RFID-encoded and interact intelligently with the MiSeq System to validate compatibility with user-defined applications. A MiSeq Reagent Kit v3 is also available. It offers a 600-cycle format to allow the longest read lengths on any Illumina sequencing system, or a 150-cycle format that enables counting applications. Specifications: Maximum Output 8.5 Gb (500-cycle MiSeq Reagent Kit v2), 5.1 Gb (300-cycle MiSeq Reagent Kit v2), 1.2 Gb (300-cycle MiSeq Reagent Micro Kit v2), 0.850 Gb (50-cycle MiSeq Reagent Kit v2), 0.5 Gb (500-cycle MiSeq Reagent Nano Kit v2), 0.3 Gb (300-cycle MiSeq Reagent Nano Kit v2) Maximum Reads per Run Up to 15 million Reagent Type Paired-End Sequencing,Cluster Generation,Sequencing by Synthesis System Compatibility MiSeq,MiSeqDx in Research Mode,MiSeq FGx in Research Mode Technology Sequencing | 19,900.00 |
| Illumina/Nextera DNA Library Prep Kit (96 samples)/FC-121-1031/1 Ea | FC-121-1031 | Illumina | 產(chǎn)品編號(hào)： FC-121-1031美 元 價(jià)： $7283.00會(huì) 員 價(jià)： 待定品 牌： Illumina產(chǎn) 地： 美國(guó)公 司： Illumina, Inc.DNA文庫(kù)制備試劑盒公司分類： Library Preparation Kits | Product Highlights: Nextera DNA Library Preparation Kits provide a fast and easy workflow, enabling sequencing-ready libraries to be generated in less than 90 minutes, with less than 15 minutes of hands-on time. Samples prepared with Nextera kits are compatIBLe with all Illumina sequencers. With Nextera technology, DNA is simultaneously fragmented and tagged with sequencing adapters in a single step, using standard lab equipment. Ideal for precious samples available in limited quantity, the protocol requires only 50 ng of DNA input. See a list of automation vendors with robotic systems compatIBLe with this kit Specifications: Assay Time 90 minutes Hands-On Time 15 minutes Input Quantity 50 ng genomic DNA (compatIBLe with most large DNA genomes) Mechanism of Action Enzymatic Fragmentation Multiplexing Up to 96 available indexes Species Category Human,Other,Mammalian,Mouse,Rat,Plant Species Details CompatIBLe with most large DNA genomes. System Compatibility MiSeq,NextSeq 550,HiSeq 3000,MiniSeq,NextSeq 500,HiSeq 2500,HiSeq 4000 Variant Class Single Nucleotide Polymorphisms (SNPs),Structural Variants,Insertions-Deletions (indels) Method Whole-Genome Sequencing Technology Sequencing Automation CapABIlity Liquid Handling Robots | 7,283.00 |
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