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    当前位置:首页 > 产品中心 > > Illumina > NP-202-1001Illumina/TruSeq Stranded mRNA Library

    Illumina/TruSeq Stranded mRNA Library

    简要描述:Illumina/TruSeq Stranded mRNA Library Prep Kit for NeoPrep (16 samples, 24 indexes)/NP-202-1001/1 Ea
    产品编号: NP-202-1001
    美 元 价: $880.00
    品 牌: Illumina
    产 地: 美国
    Library Preparation Kit

    • 产品型号:NP-202-1001
    • 厂商性质:生产厂家
    • 更新时间:2025-01-15
    • 访  问  量:1144

    详细介绍

    品牌其他品牌货号NP-202-1001
    规格16 samples, 24 indexes供货周期现货
    主要用途二代基因测序应用领域医疗卫生,食品/农产品,化工,生物产业,制药/生物制药

    Illumina/TruSeq Stranded mRNA Library Prep Kit for NeoPrep (16 samples, 24 indexes)/NP-202-1001/1 Ea

    Illumina/TruSeq Stranded mRNA Library Prep Kit for NeoPrep (16 samples, 24 indexes)/NP-202-1001/1 Ea

    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

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