Primer and method for detecting hypertension-susceptibility-related SNP site
A susceptibility and high blood pressure technology, applied in the direction of biochemical equipment and methods, recombinant DNA technology, microbial measurement/inspection, etc., can solve the problem of undiscovered high blood pressure susceptibility risk detection, and achieve high accuracy and high detection method Simple and specific effect
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[0037] 1. Collection of samples and extraction of whole genome DNA
[0038] Randomly collect 3.0 mL of peripheral blood from healthy people with EDTA-K2 anticoagulant tubes (three subjects are randomly selected as A, B and C), and use Tiangen Blood Genome Extraction Kit to extract the whole genome DNA of the subjects. The operation process According to the instructions of the kit, the concentration and purity of the obtained whole-genome DNA were detected by an ultra-trace protein and nucleic acid analyzer (BioDropμLite), and the original data was recorded. spare.
[0039] 2. PCR amplification, gel recovery, purification and sequencing of the target gene
[0040] Use the primers of FIGN gene rs16849225 site, ENPEP gene rs6825911 site primers, NPR3 gene rs1173766 site primers and TBX3 gene rs35444 site primers to perform PCR amplification on the extracted DNA respectively. As shown in Table 1;
[0041] Table 1 PCR reaction system
[0042] Reagent
Volume (μL)
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