High-flux detection method of circulating DNA liver cancer driver gene
A gene-driven, high-throughput technology, applied in the fields of biochemical equipment and methods, microbial determination/examination, etc., can solve the problems of patient pain, invasiveness, and difficulty in obtaining patient samples, and achieve strong predictability and accuracy. high effect
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[0044] A detection method of circulating tumor DNA liver cancer gene of the present invention, comprises the steps:
[0045] 1. Sample library preparation:
[0046] (1) Pipette 60 ul of purified DNA (cfDNA) and 40 ul of Endprep mix into a single PCR tube, pipette to mix, and briefly centrifuge for end repair. The reaction conditions are 30°C and 30 min.
[0047] (2) Take out the magnetic beads half an hour in advance to return to room temperature, shake and mix, take 180ul of magnetic beads and add them to the end-repaired PCR product, beat and mix, and incubate in the greenhouse for 5 minutes.
[0048] (3) Put the PCR single tube on the magnetic stand, let it stand for 5 minutes, remove the supernatant, keep the PCR tube on the magnetic stand, add 200ul of 80% ethanol (newly prepared) to rinse, let stand for 30s, remove the supernatant, 80 Rinse twice with % ethanol, and dry at room temperature for 10 minutes (with 2 minutes remaining, use a small grab to suck up the residue...
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