Method and kit for detecting rs1801131 polymorphic site genotype in MTHFR (5,10-methylenetetrahydrofolate reductase) gene
A polymorphic site and genotype technology, which is applied in biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc. low effect
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Embodiment 1
[0059] In this embodiment, a pair of primers is designed, and a mismatched base is used at the 3' end of the upstream primer, and the polymorphic site recognition sequence GAATM [M=A, C bases is formed after PCR amplification. The corresponding sequence of the mutant allele C is GAATC, which can be recognized by the restriction endonuclease HinfI; the corresponding sequence of the wild-type allele A is GAATA, which cannot be recognized by HinfI], and the downstream primers are conventional primers, which can be combined with MTHFR The 17018th to 17040th base sequence of the gene is reverse complementary. The PCR product contains an inherent HinfI recognition sequence GACTC used as an internal control for enzyme digestion. The specific plan is as follows:
[0060] 1. Genomic DNA Extraction
[0061] Using the buccal swab genomic DNA extraction kit, the genomic DNA was extracted according to the operation steps in the manual. The DNA source is not limited thereto, and any soma...
Embodiment 2
[0098] In this embodiment, the polymorphic site recognition sequence GAATM [M=A, C bases is formed by PCR amplification using mismatched upstream primers. The corresponding sequence of the mutant allele C is GAATC, which can be recognized by the restriction endonuclease HinfI; the corresponding sequence of the wild-type allele A is GAATA, which cannot be recognized by HinfI]. Amplified to form a HinfI recognition sequence used as an internal control enzyme digestion. The specific plan is as follows:
[0099] 1. Genomic DNA Extraction
[0100] Using the buccal swab genomic DNA extraction kit, the genomic DNA was extracted according to the operation steps in the manual. The DNA source is not limited thereto, and any somatic cell-derived DNA is acceptable.
[0101] 2. Primer Design
[0102] Get the sequence of 500bp before and after the rs1801131 polymorphic site of the MTHFR gene (see figure 1 , image 3 ), using PrimerPremier 5.0 software to design specific typing primers...
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