Method for carrying out blocking, substitution, amplification, enrichment and detection on target mutation based on blocker introducing extra base mismatch
A technology for detecting targets and bases, which can be used in biochemical equipment and methods, determination/inspection of microorganisms, etc., and can solve problems such as inability to meet requirements
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[0053] Example 1 provides a method for enriching and detecting the target region, and takes the detection of EGFR G719S mutation as an example to illustrate. The sample DNA used is: wild-type cfDNA and 1% mutant cfDNA (referring to sample DNA The mutated sequence containing the target mutation site accounts for 1% of the total sequence).
[0054] Including the following steps:
[0055] 1. Using the first primer, the second primer and the blocking amplification sequence to perform the first PCR amplification.
[0056] First prepare the following PCR system:
[0057] Table 1 The first PCR system
[0058]
[0059]
[0060]Among them, 2X Thermo Enzyme Mix comes from Platinum SuperFi PCR Master Mix, the manufacturer is ThermoFishier Scientific, and the article number is 00772786.
[0061] Perform the first PCR amplification according to the following PCR program:
[0062]
[0063] The primer sequences and retardation amplification sequences used were artificially synth...
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