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    Home > Food News > Enzyme News > Regarding digital PCR, please keep these dry goods [experience comment]

    Regarding digital PCR, please keep these dry goods [experience comment]

    • Last Update: 2021-08-10
    • Source: Internet
    • Author: User
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    Compared with traditional qPCR, digital PCR (dPCR) is a highly sensitive existence that can achieve absolute quantification of nucleic acids and detection of rare alleles


    For more than 20 years, digital PCR technology has been continuously improved and has been applied in many aspects, including quantifying cancer markers, measuring viral load, distinguishing genome mutations, verifying the results of next-generation sequencing, gene expression analysis, transgene detection, and environmental monitoring, etc.


    Sample Preparation

    How much starting DNA to use

    The starting amount of DNA will depend on the digital PCR system you are using


    Concentrate FFPE samples before amplification

    When dealing with highly degraded DNA, such as FFPE samples, there may be a big difference between quantifiable DNA and amplifiable intact DNA


    experimental design

    Reduce heating and cooling rate

    Nowadays, the heating and cooling rate of thermal cyclers is staggering


    Modify PCR amplification conditions

    When dealing with tricky templates, PCR cycle conditions can be changed


    • For longer amplicons (> 400 bp), change the two-step or three-step operation and add a 72°C extension cycle for 1-6 minutes, depending on the length of the amplicon



    data analysis

    Looking for real positive samples

    In order to determine whether a sample is truly positive, Bio-Rad has a good suggestion


    When detecting rare DNA, 7-10 μg of DNA may be required


    Understanding error bars

    In the ddPCR system, the error bar for each well represents a 95% confidence interval


    More suggestions

    Digest the sample

    When the amount of gDNA exceeds 66 ng, it is recommended to use restriction enzymes for digestion


    Digestion can be carried out directly in the ddPCR mixture


    Use multiple reference genes

    When evaluating copy number variation (CNV), especially cancer samples, it is necessary to ensure that the reference test is stable at 2 copies per genome


    Concluding remarks

    Nowadays, the scientific community requires higher data accuracy and more reliable results.


    In-depth understanding of Bio-Rad's droplet digital PCR system


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