Multiple-gene helicobacter pylori detection system and kit and application thereof
A Helicobacter pylori and gene detection technology, applied in the biological field, can solve the problems of relying on isolated and cultured strains, cumbersome operations, and low throughput, so as to guide individualized medication and curative effect monitoring, avoid mutual interference, and compensate for low throughput. Effect
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[0051] 1. Composition of the kit
[0052] The Helicobacter pylori detection kit in this embodiment includes: primer mixture, PCR buffer (10×PCRBuffer), MgCl 2 Solution, dNTPs, fluorescent universal label mix, hot-start DNA polymerase (Taq DNA polymerase), positive and negative controls. 2 mmol / L dNTPs and fluorescent universal label mixture are mixed together to form a reagent tube.
[0053] PCR buffer, dNTPs, and hot-start DNA polymerase were obtained from Takara (Cat. No. R007A).
[0054] Positive controls are plasmid mixtures that include all gene targets of interest.
[0055] The negative control solution was nuclease-free ultrapure water.
[0056] The primer mix includes forward primer for 16SrRNA gene, reverse primer for 16SrRNA gene, forward primer for cagA gene, reverse primer for cagA gene, forward primer for vacA-s1 or vacA-s2 gene, Reverse primer for vacA-s1 or vacA-s2 gene Forward primer for vacA-m1 gene, reverse primer for vacA-m1 gene, forward primer for vacA...
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