Rapid gene detection kit and rapid gene detection method for sudden cardiac death
A technology for sudden cardiac death and genetic testing, applied in biochemical equipment and methods, microbiological measurement/inspection, etc., can solve problems such as increasing the risk of sporadic atrial fibrillation
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Embodiment 1
[0131] Amplification reagents consist of components in the following volumes:
[0132]
[0133]
[0134] The internal reference upstream primer is SEQ NO.1, the polymorphic primer is SEQ NO.2 and SEQ NO.3, the downstream primer is SEQ NO.4, the concentration of the internal reference upstream primer is 10uM, and the polymorphic primer The concentration of the primer is 10uM, and the concentration of the downstream primer is 10uM.
[0135] The PCR amplification procedure is as follows:
[0136]
[0137] (3) Perform agarose gel electrophoresis analysis.
Embodiment 2
[0139] Amplification reagents consist of components in the following volumes:
[0140]
[0141]
Embodiment 3
[0143] Amplification reagents consist of components in the following volumes:
[0144]
[0145] In order to verify the above information, the amplification product can be detected and analyzed on the ABI3130 Genetic Analyzer to verify the above detection results of the present invention.
[0146] The loading mixture is composed of deionized formamide and molecular weight internal standard. Mix 10ul of the loading mixture with 1ul of the amplification product or allele analysis standard to avoid bubbles, denature at 95°C for 5min, perform electrophoresis, and use ABI3130 for genetic analysis. Instrument detection and analysis to verify the analysis results.
[0147] The amplification is performed by AS-PCR (allele-specific PCR), and polymorphism typing is detected by agarose gel electrophoresis.
[0148] The human genomic DNA detected is the DNA obtained by processing the source sample using the Chelex method, magnetic bead extraction method or phenol / chloroform extraction ...
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