Primer and method for detecting rectal-cancer-susceptibility-related SNP site
A technology for susceptibility and rectal cancer, applied in the direction of biochemical equipment and methods, recombinant DNA technology, microbial measurement/inspection, etc., to achieve good specificity, good accuracy, and high specificity
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[0034] 1. Collection of samples and extraction of whole genome DNA
[0035] Use an EDTA anticoagulation tube to collect 3.0 mL of peripheral blood from healthy people (three subjects are randomly selected), and use Tiangen Blood Genome Extraction Kit to extract the subject's whole genome DNA. The operation process is performed according to the kit instructions. The concentration and purity of the whole genomic DNA are detected by an ultra-microprotein nucleic acid analyzer (BioDropμLite), the original data is recorded, and the DNA with the required concentration and purity is stored in the refrigerator at -20℃ for later use.
[0036] 2. PCR amplification, gel recovery, purification and sequencing of the target gene
[0037] PCR amplification of the target gene was performed with the primers at rs3802842 site of C11orf93 gene, the primers at rs4939827 site of SMAD7 gene, the primers at rs6983267 site of POU5F1B gene and the primers at rs10795668 site of RNA5SP229 gene, respectively. ...
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