Quantitative Multiplex Reference Standard fcDNA (severe)

Quantitative Multiplex Reference Standard fcDNA (severe)

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    商品描述
    The Quantitative Multiplex Formalin Compromised DNA Reference Standards (Mild, Moderate and Severe) provide biologically-relevant quality control material which can be used to assess the performance of NGS assays. These Formalin-Compromised DNA Standards vary in levels of fragmentation and formalin damage providing the ability to challenge your assay.
    组成成分
    定量多重福尔马林受损脱氧核糖核酸,水,Tris-EDTA缓冲液(三羟甲基氨基甲烷,乙二胺四乙酸)

    Next generation sequencing (NGS) platforms give researchers much greater power when profiling tumor samples. However, the use of NGS presents challenges surrounding sample variability, platform bias, and potential failure to detect biomarkers. Horizon’s standards are appropriate for any NGS library preparation including whole-genome, whole-exome, custom capture and targeted amplicon panels. Horizon has developed this Quality-Seq (Q-Seq) NGS Reference Standard range to support the development and continued validation of Next Generation Sequencing platforms. The Quantitative Multiplex Reference Standard (QMRS) portfolio covers multiple endogenous SNPs, insertions and deletions. The QMRS includes 11 mutations at 0.8-24.5% allelic frequency in genomic DNA, FFPE and Formalin-Compromised DNA format. The multiple formats of the QMRS allow you to validate both the pre-analytical and analytical portion of your workflow using an isogenic reference standard. The FFPE format QMRS allows you to evaluate and optimize DNA extraction protocols without wasting precious patient samples. With the Formalin-Compromised format, the robustness of your NGS workflow may be tested to ensure that your library protocol and informatics pipeline can accommodate these highly degraded samples. The QMRS standard is our most popular multiplex standard as it provides both a breadth of formats, but also a large range of allelic frequencies and onco-relevant mutants.

    With this product you are able to:

    • Evaluate the effect of formalin on your assay
    • Analyze the robustness of your workflow with multiple formats (DNA , FFPE and Formalin-Compromised DNA)
    • Optimize and validate new cancer panels and routinely monitor the performance of your assay

     

    Technical Data

    Format: Formalin-Compromised DNA

    Genes Covered: BRAF, KIT, EGFR, KRAS, NRAS, PIK3CA

    Allelic Frequencies: 1% - 24.5% for verified variants

    Buffer: Tris-EDTA (10mM Tris-HCl, 1mM EDTA), pH 8.1

     

    Product Information

    Verified Mutations:

    Chromosome

    Gene

    Variant

    Expected Allelic Frequency, %

    7q34

    BRAF

    V600E

    10.50%

    4q11-q12

    cKIT

    D816V

    10.00%

    7p12

    EGFR

    ΔE746 - A750

    2.00%

    7p12

    EGFR

    L858R

    3.00%

    7p12

    EGFR

    T790M

    1.00%

    7p12

    EGFR

    G719S

    24.50%

    12p12.1

    KRAS

    G13D

    15.00%

    12p12.1

    KRAS

    G12D

    6.00%

    1p13.2

    NRAS

    Q61K

    12.50%

    3q26.3

    PIK3CA

    H1047R

    17.50%

    3q26.3

    PIK3CA

    E545K

    9.00%

    Presence confirmed in parental cell line

    Chromosome

    Gene

    Variant

    Expected Allelic Frequency, %

    2p23

    ALK

    P1543S

    33%

    1q25.2

    ABL2

    P986fs

    8%

    5q21-q22

    APC

    R2714C

    33%

    1p35.3

    ARID1A

    p.M1564fs*1

    33.50%

    13q12.3

    BRCA2

    K1691fs

    33%

    13q12.3

    CDX2

    V306fs

    41.50%

    22q13.2

    EP300

    K292fs

    8%

    4q31.3

    FBXW7

    S668fs

    33.50%

    8p12

    FGFR1

    P150L

    8.50%

    13q12

    FLT3

    V197A

    11.50%

    2q33.3

    IDH1

    S261L

    10%

    7q31

    MET

    L238fs

    6.50%

    3p21.3

    MLH1

    L323M

    8.50%

    17q11.2

    NF1

    Y628fs

    7.50%

    22q12.2

    NF2

    P275fs

    8%

    9q34.3

    NOTCH1

    P668S

    31.50%

    1q21-q22

    NTRK1

    5'UTR (1:156815754, GRCh38)

    8.50%

    4q12

    PDGFRA

    G426D

    33.50%

    Unit Size: 1 µg

    Concentration: 50 ng/µl

     

    General Information

    Storage: 4˚C

    Expiry: See all product shelf life information

     

    Quality Control 

    Allelic Frequency: Droplet Digital PCR™

    Quality: TapeStation gDNA ScreenTape Assay. 

    Product HD803, batch 43986, was found to have a DIN value of 2.3, which falls outside of current specification of  ≤2.0.To explain this further the DNA fragment Length: Batch 43986 has an average fragment length of 478bp, the average fragment length for previous released batches of HD803 is 355bp ±93.9. As a reference, for HD799 product (moderate) the average DNA fragment length is 1874bp ±456.2. Please contact Scientific Support for further information.

    Quantification: Qubit dsDNA BR Assay

    Intended use: For assay developers and molecular diagnostic labs for routine performance monitoring of molecular biology assays. Research use only. Not for diagnostic procedures.

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    货号:
    HD803
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