A primer and method for quickly distinguishing small yellow croaker from large yellow croaker and determining hybrids between small yellow croaker and large yellow croaker
A technology for large yellow croaker and small yellow croaker, applied in biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc. problem, to achieve the effect of a quick identification method
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[0016] (1) Select small yellow croaker, large yellow croaker and hybrid fish [small yellow croaker (♀) and large yellow croaker (♂)] for professional morphological identification;
[0017] (2) Extract the DNA of small yellow croaker, large yellow croaker and hybrid fish samples by phenol-chloroform extraction method;
[0018] (3) The PCR amplification reaction system is: 10×Buffer 2.5 μl, dNTP 2.0 μl, Taq enzyme 0.2 μl, upstream primer and downstream primer 1 μl, DNA template 1 μl, ddH2O 18.3 μl; PCR amplification reaction conditions are: 94°C After pre-denaturation for 5 minutes, enter 35 cycles: 94°C for 35sec, 59°C for 35sec, 72°C for 1.0min; finally, extend at 72°C for 10min;
[0019] Upstream primer: 5'- GGTGGTGGCAAAATTTGATT -3' (as shown in SEQ ID No.1);
[0020] Downstream primer: 5'-CCACACACCTAATGCCTCCT-3' (as shown in SEQ ID No.2);
[0021] (3) Electrophoresis staining comparison pattern: After the PCR reaction, 8 μL of the product was detected by agarose gel electr...
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