Detection method for 19-bp duplication and deletion polymorphism of Chinese yellow cattle PLAG1 (Pleomorphic Adenoma Gene 1) gene and application of detection method
A PLAG1, 19-bp technology, which is applied in the determination/testing of microorganisms, biochemical equipment and methods, recombinant DNA technology, etc., can solve the problems of low mutation frequency, long reproduction and breeding cycle, genetic resource limitation, etc., and achieve low cost effect
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[0030] This embodiment provides a kind of using the whole genome DNA of Chinese yellow cattle as a template, using primer pair P1 to amplify a partial fragment of PLAG1 gene of Chinese yellow cattle by PCR; then carry out agarose gel electrophoresis to the fragments obtained by PCR amplification; identify according to the electrophoresis results The genotype of the insertion / deletion polymorphic site on the PLAG1 gene of Chinese yellow cattle;
[0031] The primer pair P1 is:
[0032] Upstream primer: 5'-GATCCCACCTGACAAACG-3';
[0033] Downstream primer: 5'-CTAGAGCTGCCTCGCACA-3'.
[0034] Wherein, the insertion / deletion polymorphic site on the Chinese cattle PLAG1 gene refers to the 19-bp repeat deletion polymorphic fragment GAACACACAGCCCACAAGG present on the AC_000171.1g.3747444-3747462 site of the Chinese cattle PLAG1 gene.
[0035] In this example, the reaction program of PCR amplification is: pre-denaturation at 95.0°C for 5 minutes; denaturation at 95.0°C for 30s, annealin...
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