Kit for predicting susceptibility to sudden cardiac death
A technology for sudden cardiac death and kits, which is applied in the determination/examination of microorganisms, biochemical equipment and methods, DNA/RNA fragments, etc., can solve the problem of not predicting the susceptibility of SCD and diagnosing SCD.
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Embodiment 1
[0041] A kit for predicting susceptibility to sudden cardiac death of the present invention, comprising a fluorescent dye-labeled specific primer pair for detecting the insertion / deletion polymorphism site rs3917 on the COL1A2 gene, rs72014506 on the MIR155HG gene The specific primer pair for the insertion / deletion polymorphic site, the specific primer pair for the insertion / deletion polymorphic site rs113044851 on the CTH gene, and the specificity for the insertion / deletion polymorphic site rs397729601 on the DSG2 gene primer pair. in
[0042] The specific primer pair for the rs3917 insertion / deletion polymorphic site on the COL1A2 gene uses the sequence shown in SEQ ID No.1 as a sense primer, and uses the sequence shown in SEQ ID No.2 as an antisense primer;
[0043] The specific primer pair for the rs72014506 insertion / deletion polymorphic site on the MIR155HG gene uses the sequence shown in SEQ ID No.7 as a sense primer, and uses the sequence shown in SEQ ID No.8 as an an...
Embodiment 2
[0069] The test kit for predicting susceptibility to sudden cardiac death in Example 1 of the present invention is used in the same manner as in Example 1, and its diagnosis of SCD is as follows:
[0070] The gene sequencing diagrams and SDS-PAGE gel electrophoresis diagrams of COLIA2 gene, MIR155HG gene, CTH gene and DSG2 gene are as follows Figure 1-4 shown. In the figure, A is an example of the sequencing results of the template strand, and the underline corresponds to the indel of the coding strand at the polymorphic site; B is from different individuals (numbered 1-14, where numbers 1, 2, 3, 8, 9, and 10 No. 1 sample is diagnosed as sudden cardiac death by forensic pathology anatomy, and the remaining samples are normal control group) DNA samples using the PCR amplification system of the present invention to obtain a schematic diagram of product electrophoresis.
[0071] figure 1 It shows that numbers 1 and 8 are deletion homozygotes, numbers 2, 4, 5, 6, 7, 11, 12, 13 an...
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