4000-520-616
欢迎来到免疫在线!(蚂蚁淘生物旗下平台)  请登录 |  免费注册 |  询价篮
主营:主营:分子类化合物
咨询热线电话
4000-520-616
当前位置: 首页 > 产品中心 > peptide > Qiagen/QIAseq靶向RNA索引/包含样本索引的试剂盒,足以为总共48个样本编制索引,用于在Illumina平台(试管格式)上为靶向RNA测序编制多达12个样本的索引,以及生成的RNA文库测序所需的引物
商品详细Qiagen/QIAseq靶向RNA索引/包含样本索引的试剂盒,足以为总共48个样本编制索引,用于在Illumina平台(试管格式)上为靶向RNA测序编制多达12个样本的索引,以及生成的RNA文库测序所需的引物
Qiagen/QIAseq靶向RNA索引/包含样本索引的试剂盒,足以为总共48个样本编制索引,用于在Illumina平台(试管格式)上为靶向RNA测序编制多达12个样本的索引,以及生成的RNA文库测序所需的引物
Qiagen/QIAseq靶向RNA索引/包含样本索引的试剂盒,足以为总共48个样本编制索引,用于在Illumina平台(试管格式)上为靶向RNA测序编制多达12个样本的索引,以及生成的RNA文库测序所需的引物
商品编号: 333114
品牌: Qiagen
市场价: ¥8620.00
美元价: 5172.00
产地: 美国(厂家直采)
公司:
产品分类: 多肽合成
公司分类: peptide
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

QIAseq Targeted RNA Indexes

Product picture

For indexing samples for targeted RNA sequencing and primers necessary for sequencing RNA libraries generated by the QIAseq Targeted RNA Panels

    • Sample indexes to index up to 96 samples for Illumina and Ion Torrent sequencers
    • Enough of each index for four samples
    • Tube format for flexibility and array format for convenience and high-throughput

    Need a quote for your research project or would you like to discuss your project with our specialist team? Contact Us

    • Buy Products
    • Product Details
    • Product Resources

    Buy Products

    Cat No./ID:333114
    QIAseq Targeted RNA 12-Index I (48)
    $431.00
    Order Product
    Kit containing sample indexes, enough for a total of 48 samples, for indexing up to 12 samples for targeted RNA sequencing on Illumina platforms (tube format), and primers necessary for sequencing RNA libraries generated by the QIAseq Targeted RNA Panels on Illumina platforms
    Cat No./ID:333117
    QIAseq Targeted RNA 96-Index I (384)
    $1,296.00
    Order Product

    Kit containing sample indexes, enough for a total of 384 samples, for indexing up to 96 samples for targeted RNA sequencing on Illumina platforms (tube format), and primers necessary for sequencing RNA libraries generated by the QIAseq Targeted RNA Panels on Illumina platforms

    Cat No./ID:333127
    QIAseq Targeted RNA 96-Index HT l (384)
    $1,296.00
    Order Product

    Kit containing sample indexes, enough for a total of 384 samples, for indexing up to 96 samples for targeted RNA sequencing on Illumina platforms (array format), and primers necessary for sequencing RNA libraries generated by the QIAseq targeted RNA panels on Illumina platforms

    Cat No./ID:333214
    QIAseq Targeted RNA 12-Index L (48)
    $431.00
    Order Product
    Kit containing sample indexes, enough for a total of 48 samples, for indexing up to 12 samples for targeted RNA sequencing on Ion Torrent platforms (tube format)
    Cat No./ID:333217
    QIAseq Targeted RNA 96-Index HT L (384)
    $1,296.00
    Order Product

    Kit containing sample indexes, enough for a total of 384 samples, for indexing up to 96 samples for targeted RNA sequencing on Ion Torrent platforms (array format)

    QIAseq Targeted RNA Indexes are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.

    Product Details

    9
    One solution to overcome the challenges of gene expression profiling

    The QIAseq Targeted RNA Panels have been developed as a Sample to Insight solution for quantitative gene expression profiling using RNAseq. The panels use molecular barcodes and a two-stage PCR-based integrated library preparation to overcome the challenge of PCR duplicates and amplification bias to deliver unbiased, accurate and reproducible gene expression results.

    9
    High concordance with qPCR
    Expression levels for 384 genes were determined by both QIAseq Targeted RNA Panel and qPCR for Human Brain Reference RNA (HBRR) and Universal Human Reference RNA (UHRR) samples. The expression levels determined by qPCR were normalized to the average of four housekeeping genes (ACTB, B2M, GAPDH and RPLP0) and fold change between the samples was calculated (HBRR/UHRR) for each gene. For QIAseq, the number of unique molecular barcodes per gene were counted and normalized to average number of molecular barcodes for the four housekeeping genes for each sample. The fold change for each gene was then calculated. The QIAseq Targeted RNA Panel and qPCR assays exhibit similar fold-changes in gene expression, highlighting the accuracy of QIAseq-results.
    9
    Proprietary primer design delivers gene-specific amplicons (>97% specificity)

    Sequencing libraries were prepared using 1.25, 5 or 20 ng universal reference RNA and QIAseq Targeted RNA Panels, ranging from 12-plex to 1000-plex. Sequencing was performed on the Illumina MiSeq, dedicating 1 million reads per sample. Specificity is calculated as percent of trimmed and mapped reads that map to intended targets.

    9
    Simple procedure

    Starting with 25 ng of total unfragmented RNA, cDNA is synthesized, and each cDNA molecule is tagged with a unique molecular barcode before any amplification. The uniquely tagged cDNA molecules then undergo a two-stage PCR step for enrichment and library construction. It takes only 6 hours from RNA sample to targeted library ready for sequencing.

    9
    Unmatched uniformity (>97% of assays are within 20% of median molecular tag counts)
    A 917-plex gene panel was used to prepare a library from 10 ng of NA12878 reference DNA. All assays were designed to be intra-exon, and are thus single copy on genomic DNA. This allows an estimation of the uniformity of amplicon performance in the library preparation step (e.g., every unique tag equals one captured copy). In terms of raw assay performance, 97.5% of assays are within 20% of mean/median molecular tag counts. For cataloged panels, any assay below 20% is redesigned and replaced. Molecular barcodes entirely remove this variation in RNAseq counting.
    9
    Unbiased and accurate gene quantification (B)
    Different amounts (20 ng, 5 ng or 1.25 ng) of universal reference RNA were used to determine expression levels of three genes (BNIP1, CTNND2 and DAPK1) using targeted RNAseq. QIAseq digital RNA sequencing method (A; molecular barcode counts) showed accurate quantification of all three genes corresponding to different RNA input, whereas traditional targeted RNAseq (B; read counts) revealed PCR duplication limitation and yielded inaccurate quantification.
    9
    Unbiased and accurate gene quantification (A)

    Different amounts (20 ng, 5 ng or 1.25 ng) of universal reference RNA were used to determine expression levels of three genes (BNIP1, CTNND2 and DAPK1) using targeted RNAseq. QIAseq digital RNA sequencing method (A; molecular barcode counts) showed accurate quantification of all three genes corresponding to different RNA input, whereas traditional targeted RNAseq (B; read counts) revealed PCR duplication limitation and yielded inaccurate quantification.

    9
    Digital sequencing (molecular barcodes) principle

    QIAseq Targeted RNA Panels use a digital sequencing method, whereby a unique 12-base random molecular barcode incorporated into the gene-specific primers (GSP1) is used in the first extension step (after mRNA is converted to cDNA). Thus, every extension event yields a unique combination of molecular barcode and target sequence. At the end of sequencing, the relative amount of each mRNA target is determined by the number of unique molecular barcode-target combinations that were sequenced, thereby eliminating PCR duplicates and amplification bias, resulting in more accurate,unbiased gene expression analysis.

    9
    Positive results with as little as 0.2 copies of RNA per cell
    ERCC standards, at 86 to 705,500 copies, spiked into universal reference RNA sample and enriched using 384-plex QIASeq Targeted RNA Panel in three technical replicates. (A) Sensitivity measurement. Under standard conditions (20 ng RNA input, 0.5 million MiSeq reads), ≥~100 copies of ERCC transcripts were reliability detected, which is the equivalent of ~0.2 copies per cell. (B) Precision measurement. At >10 barcodes/gene, CV was less than 5% for all targets, indicating high technical reproducibility. This corresponds to ~100 copies target RNA in the sample.
    Performance
    • Accuracy: Innovative digital sequencing (molecular barcode counting) eliminates PCR duplication and amplification bias to deliver the most accurate results (see figure Unbiased and accurate gene quantification) .
    • Specificity: The unique combination ofour proprietary primer design algorithm and rigorous testing of every primer assay guarantees high specificity and accurate results (see figure Proprietary primer design delivers gene-specific amplicons – 97% specificity).
    • Uniformity: The QIAseq Targeted RNA Panel workflow has been optimized to deliver highly uniform sequencing results, to ensure sequencing capacity is utilized very efficiently. In fact, digital sequencing (molecular barcodes) entirely remove this variation in RNAseq counting (see figure Unmatched uniformity – 97% of assays are within 20% of median molecular tag counts).
    • Reproducibility: The QIASeq Targeted RNA Panel system demonstrates strong correlations across technical replicates, product lots and instruments with correlation coefficients averaging above >0.99, to ensure reliable detection of differences in expression between biological samples
    • Sensitivity: Digital RNA sequencing system is optimized to deliver highly reliable quantification down to ~100 copies of an RNA target in 25 ng total RNA (see figure Positive results with as little as 0.2 copies of RNA per cell).
    • Flexibility: QIAseq panels combine the power of NGS with the accuracy of qPCR to allow multiplexing of several samples per NGS while delivering cost-effective results (see figure Simple procedure).
    Principle
    • Traditional RNA sequencing methods suffer from PCR duplication and amplification bias, resulting in inaccurate gene expression analysis. By introducing molecular barcodes before any amplification takes place, QIAseq Targeted RNA Panels are able to eliminate this issue to deliveraccurate and digital quantification of genes (see figure Unbiased and accurate gene quantification).
    • A unique feature of the QIAseq Targeted RNA Panels is the set of built-in control assays. The gDNA assays control for any gDNA contamination in the RNA sample to ensure reproducible results. The housekeeping gene (HKG) assays are used to normalize data, thereby making sample-to-sample and run-to-run comparisons possible.

      Procedure
      • The QIAseq Targeted RNA Panels workflow begins with converting total RNA into cDNA (see figure Simple procedure). The workflow requires minimal RNA input: as little as 25 ng total RNA can be used. No enrichment or depletion steps are necessary. The molecular barcoding step makes use of molecularly barcoded gene-specific primer (GSP1) in a multiplex primer panel (targeting 12-1000 genes) and an input of 20ng of cDNA equivalent (cDNA made from 20 ng of total RNA). After the barcoding step, the uniquely tagged cDNA is purified over beads to remove residual primers, and a PCR is set up with a second pool of gene-specific adapter primers (GSP2) and the RS2 primer, which primes off of a common tag on the GSP1 primers. This reaction insures that intended targets are enriched sufficiently to be represented in the final library. The number of cycles is kept to a minimum to keep PCR-induced variations in amplification to a low level (any variations are easily corrected and accounted for with the molecular barcodes). Another quick cleanup with beads is performed, and a universal PCR is run with RS2 and FS2 primers, which also adds sample-indexing barcodes to each sample. A final cleanup with beads is performed and the library is complete, and ready for quantification and sequencing.
      • An integral component of the QIAseq Targeted RNA Panels is data analysis and insight. Data analysis modules have been developed that are comprehensive, yet easy to use. Using these modules require no bioinformatics expertise. Starting with raw reads directly off the sequencer, the QIAseq targeted RNA data analysis tools at QIAGEN’s GeneGlobe portal, provide you with gene counts and fold changes, as well as links for pathway analysis.
      Applications
      • Biomarker research
      • Confirmation of whole transcriptome sequencing data
      • Confirmation of microarray data

      Product Resources

      You are not authorized to download the resource

      Kit Handbooks (1)
      • Sort options
        • Sort alphabetically
      QIAseq Targeted RNA Panels Handbook
      Show details
      Instrument Technical Documents (2)
      • Sort options
        • Sort alphabetically
      QIAseq Targeted RNA Panels Template for MiSeq
      Show details
      QIAseq Targeted RNA Panels Template for NextSeq
      Show details
      Safety Data Sheets (5)
      • Sort options
        • Sort alphabetically
      MSDS QIAseq Targeted RNA 12-Index L (48)
      MSDS QIAseq Targeted RNA 96-Index HT l (384)
      MSDS QIAseq Targeted RNA 96-Index HT L (384)
      MSDS QIAseq Targeted RNA 12-Index I (48)
      MSDS QIAseq Targeted RNA 96-Index I (384)
      fragment fix placeholder

      Customers who bought these products also bought

      • Cat No./ID:333502
        /us/products//discovery-and-translational-research/next-generation-sequencing/dna-sequencing/whole-genome-sequencing/qiaseq-targeted-dna-panels/

        QIAseq Targeted DNA Panel (12)

        Kit containing ALL reagents (except indexes) for targeted DNA sequencing; fixed panel for 12 samples; less than 100 genes
        Select Targets
      • Cat No./ID:56404
        /us/products//top-sellers/qiaamp-dna-ffpe-tissue-kit/

        QIAamp DNA FFPE Tissue Kit (50)

        For 50 DNA preps: 50 QIAamp MinElute Columns, Proteinase K, Buffers, Collection Tubes (2 ml)
        $256.00
        Add To Cart
      品牌介绍
      QIAGEN是一家专业化致力于生物分子样品制备解决方案的跨国经营企业,总部位于德国。1984年,QIAGEN在德国成立,1996年在美国纽约纳斯达克上市。QIAGEN拥有超过1000项专利和认可证明,在18个国家设立了分公司,代理商服务国超过40个,在全球有超过400000的用户。QIAGEN提供的产品超过500类,包括各种试剂,耗材和自动化纯化工作站。这些产品用于样品采集,稳定,核酸或蛋白的分离,纯化和检测中,不仅广泛的应用于科研领域的各个方面,在生物技术,制药,法医研究,食品安全检测,畜牧业和分子诊断领域也得到了广泛的应用。QIAGEN产品的卓越品质和在应用中的出色表现使得其成为样品处理中标准的代名词。