Aspirin individualized drug gene detection kit and detection method
An aspirin and gene detection technology, which is applied in the field of detection kits for the detection of aspirin personalized medicine gene detection kits, and achieves high accuracy, accurate treatment and prevention of cardiovascular events, and the effects of precise treatment and prevention of cardiovascular events.
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Embodiment 1
[0045] Genetic detection kit for one-person detection of aspirin individualized medicine, including the following components:
[0046] (1) 4 pairs of primers for amplification and sequencing of PTGS1 (-842A>G), ITGA2 (759C>T), ITGB3 (176T>C) and PEAR1 (-9-3996G>A), each primer 1OD.
[0047] The nucleotide sequences of each primer are shown in SEQ NO.5-12, see Table 1 for details:
[0048] Table 1: Primer sequences
[0049]
[0050] (2) PCR amplification reagent: 15 μL of Taq enzyme mixture (dNTP, 10×PCR reaction buffer, MgCl 2 ) (purchased from Novozyme);
[0051] (3) PCR product purification reagent: 3.2 μL SAP enzyme mixture (SAP enzyme, ExoI enzyme, deionized water) (purchased from Novizyme);
[0052] (4) Sequencing reagents: 4.4 μL BigDye mix (Bigdye, 5×seq), 5 μL EDTA, 60 μL ethanol solution (100%), 200 μL ethanol solution (70%), 16 μL Hi-Di.
[0053] This kit is stored at -20°C, and repeated freezing and thawing should be avoided as much as possible.
Embodiment 2
[0055] Using the one-person detection aspirin individualized drug gene detection kit in Example 1, the steps are as follows:
[0056] (1) extract the genomic DNA of the sample;
[0057] (2) PCR amplification of PTGS1(-842A>G), ITGA2(759C>T), ITGB3(176T>C) and PEAR1(-9-3996G>A) loci
[0058] For PTGS1 (-842A>G), ITGA2 (759C>T), ITGB3 (176T>C) and PEAR1 (-9-3996G>A) sites, design primers according to Table 1 of Example 1 for PCR amplification.
[0059] Each reaction system has a total volume of 16 μL, including 7.5 μL of Taq enzyme mixture (dNTP, 10×PCR reaction buffer, MgCl 2 ), deionized water 5.5 μL, primer pair (10uM) 1 μL, genomic DNA (100ng / ul) 1ul. The reaction conditions are 95°C for 15 minutes, 14 cycles (-0.5°C / cycle) of 94°C for 30 seconds, 63°C for 30 seconds, and 72°C for 45 seconds; then 30 cycles of 94°C for 30 seconds and 56°C for 30 seconds , 72°C for 45 seconds, and finally 72°C for 10 minutes.
[0060] (3) Purification of PCR products
[0061] Each reacti...
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