Gene polymorphism detection primer set, kit and detection method of caffeine metabolic capacity related gene CYP1A2
A CYP1A2, gene polymorphism technology, used in biochemical equipment and methods, recombinant DNA technology, and microbial assay/inspection, etc. problem, to achieve the effect of short time, not easy to contaminate, and high sensitivity
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Embodiment 1
[0028] A primer set for detecting polymorphism of CYP1A2 gene related to caffeine metabolism capacity, including the following primers:
[0029] Detection primer 1: 5'-AAGGGTGAGCTCTGTGGCTC-3' (SEQ ID NO.1);
[0030] Detection primer two: 5'-AAGGGTGAGCTCTGTGGCTA-3' (SEQ ID NO. 2);
[0031] Detection primer three: 5'-CCAGGCAGAAGATGGCAGAG-3' (SEQ ID NO.3);
[0032] Internal control primer 1: 5'-AGCAAGCAGGAGTATGACG-3' (SEQ ID NO.4);
[0033] Internal control primer 2: 5'-GAAAGGGTGTAACGCAACT-3' (SEQ ID NO. 5).
[0034] The detection primers and internal control primers described in this embodiment are all synthesized by biotechnology commonly used in the art.
Embodiment 2
[0036] Such as figure 1 As shown, a kit for detecting the polymorphism of the CYP1A2 gene related to caffeine metabolism capacity includes the five primers described in Example 1. The kit also includes a PCR reaction premix, a wild plasmid, a C5246A mutant plasmid and purified water which are respectively contained in a container. The PCR reaction premix used in this embodiment is a product sold by Tiangen Biochemical Technology (Beijing) Co., Ltd. The PCR reaction premix includes 3'→5' exonuclease activity high-fidelity Taq enzyme, 1.0-5.0mM MgCl2, 1.0-5.0mM dNTPs and SYBR Green I.
[0037] The kit includes a box body 1, the inside of the kit is divided into two independent cavities by a partition 3, and both cavities are provided with a sponge 2, the detection primer 1, the detection primer 2, the detection primer 3. Primer one, internal control primer two, PCR reaction premix, wild plasmid, C5246A mutant plasmid and purified water are respectively installed in the test tube, ...
Embodiment 3
[0040] A method for detecting the CYP1A2 gene polymorphism of the caffeine metabolism-related gene, using the detection primer 1 and the detection primer 3 of the present invention to detect the wild gene at the rs762551 site of the CYP1A2 gene, and using the detection primer 2 of the present invention And detection primers three pairs of CYP1A2 gene rs762551 mutation gene detection.
[0041] The method for detecting the polymorphism of the CYP1A2 gene related to caffeine metabolism capacity includes the following steps:
[0042] a. Mix the PCR reaction premix, detection primer one, detection primer three and water evenly to obtain reaction mixture one; mix the PCR reaction premix, detection primer two, detection primer three and water evenly to obtain reaction mixture two; Mix the PCR reaction premix, internal control primer one, internal control primer two and water evenly to obtain reaction mixture three;
[0043] b. Add the sample DNA to be tested into reaction mixture one, reac...
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