Method and special primer pair for detecting quality character of pork
A pork quality and primer pair technology, which is applied in DNA/RNA fragments, recombinant DNA technology, animal husbandry, etc., can solve the problems of pork quality decline and achieve the effects of reducing breeding costs, low cost, and simple operation
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[0031] Embodiment 1, the identification of pork quality character
[0032] 1. Determination of genetic polymorphism sites
[0033] 1. PCR amplification
[0034] Primer pairs are as follows:
[0035] U (upstream primer): 5'-TGCCTGCTCCTTAAGCTTCT-3' (sequence 1 of the sequence listing);
[0036] D (downstream primer): 5'-GGGAGGGAGGAAAACAAGAG-3' (SEQ ID NO: 2 of the Sequence Listing).
[0037] Using the genomic DNA of 3 Damin hybrid pigs as templates, PCR amplification was performed using primers U and D.
[0038] Amplification system: Genomic DNA 200ng, 10×PCR amplification buffer 5μl, dNTPs 10mM, upstream and downstream primers 50ng each, Taq DNA polymerase 0.75U, Mg 2+ 2.5mmol / L, with ddH 2 O Supplement the reaction system to 50 μl.
[0039] The PCR reaction conditions were: denaturation at 95°C for 5 min; then denaturation at 95°C for 20 s, annealing at 58°C for 30 s, and extension at 72°C for 30 s, a total of 35 cycles; finally, extension at 72°C for 10 min.
[0040] ...
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