Primer and kit for amplifying related genes of breast cancer and ovarian cancer and application thereof
A technology for ovarian cancer and breast cancer, applied in the field of biological genes, can solve the problems of incompleteness and simplicity, and achieve the effect of easy access to samples
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[0091] 1. Isolate DNA from wax block tissue samples:
[0092] 20-40μm tumor paraffin section tissue, using the modified QIAGEN kit extraction method to separate and extract DNA, and use Nanodrop2000 micro spectrophotometer to determine the concentration and purity. The extracted DNA concentration is required to be greater than 4ng / μL, and the purity is between 1.8-2.0 (260 / 280 ratio). The extracted DNA was diluted to 4ng / μL with TEBuffer.
[0093] Concrete method is as follows (NaHSO in described step 3 , NaCl, NaOH, xylene, glycerol, and ethanol solutions are all prepared with superior pure reagents from Sinopharm):
[0094] (1) Dewaxing of paraffin specimen slices: the sample mass is 15-20 mg, put the slices in a filter column, add 200 μL of high-grade pure xylene, vortex and oscillate for dewaxing for 1 min, centrifuge, discard xylene, and add xylene again for dewaxing ;
[0095] (2) Specimen hydration: Hydrate the tissue cells with absolute ethanol, 95% ethanol, 85% et...
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