Primer for detecting MiR-34b/crs4938723 mutant, and application thereof in preparation of gastric cancer screening kit
A technology of crs4938723 and mutants, applied in the preparation of gastric cancer screening kits, the field of primers for detecting MiR-34b/c rs4938723 mutants, can solve the problem of no risk relationship of gastric cancer and the like
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[0015] Example 1: Take 3 mL of peripheral blood from a subject, and use a whole blood genomic DNA extraction kit (Tiangen, Beijing, China) to extract the subject's genomic DNA. Subsequent PCR amplification technique was used to amplify the fragment of interest in a 20 μL reaction mixture including: 1.625 mM MgCl 2 , 0.14mM dNTPs, 1U Taq enzyme (MBI Fermentas), 2μL×10PCR buffer (MBI Fermentas), 200ng of the subject’s genomic DNA and 10uM primers (sense: 5'-CCTCTGGGAACCTTCTTTGACCAAT-3', antisense: 5' -TGAGATCAAGGCCATACCATTCAAGA-3'). The PCR reaction conditions were initially 95°C denaturation for 5 minutes, 95°C for 30 seconds, 54°C for 30 seconds, 72°C for 1 min, a total of 34 cycles to amplify DNA, and finally 72°C for 10 minutes. A 148bp PCR product of miR-34b / c rs4938723 was obtained. The amplified PCR product was continuously digested with restriction enzyme MLuCI (New England BioLabs, Beverly, MA) at 37°C for 16 hours, then separated on an 8% polyacrylamide gel, and 1.0 ...
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