Primer and method for identifying pseudosciaena crocea of daiqu species and min-yuedong species
A technology of large yellow croaker and Daiqu family, which is applied in the field of biotechnology species identification, can solve the problems of unstable RAPD technology system and low repeatability, and achieve the effects of fast identification, low false positive rate and good repeatability
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specific Embodiment 2
[0041] A kind of identification method of Daiqu large yellow croaker and Fujian-Yuedong large yellow croaker of the present invention, concrete steps are as follows:
[0042] (1) Extraction and quantitative detection of total DNA of large yellow croaker
[0043] (2) Preparation of PCR amplification system
[0044] The preparation of the PCR amplification reaction system is as follows: various components and final concentrations are: buffer 10mM, dNTP 0.2mM, Mg 2+ 2mM, each primer is 0.2mM, Taq enzyme 1U, large yellow croaker template DNA 10-50ng, make up to 25ul with double distilled water, the primer sequence is:
[0045] J1 upstream primer 5′-GGCATTTAGGCACAAGGAC-3′
[0046] J1 downstream primer 5′-GGGGGCACAACTCAGAGG-3′
[0047] J2 upstream primer 5′-CAGGCCCCACCATACTAGT-3′
[0048] J2 Downstream Primer 5′-GGGTGCCGGTTCCTGAC-3′
[0049] (3) PCR amplification reaction
[0050] Heat on the PCR instrument at 95°C for 2-5min to fully denature the template DNA, then enter the...
specific Embodiment 3
[0053] A kind of identification method of Daiqu large yellow croaker and Fujian-Yuedong large yellow croaker of the present invention, concrete steps are as follows:
[0054] (1) DNA extraction and quantitative detection of large yellow croaker by phenol-chloroform extraction method
[0055] (2) Preparation of PCR amplification system
[0056] The preparation of the PCR amplification reaction system is as follows: various components and final concentrations are: buffer 10mM, dNTP 0.2mM, Mg 2+ 2mM, each primer is 0.2mM, Taq enzyme 1U, 10ng of large yellow croaker template DNA in the PCR amplification reaction system of primer pair J1, 40ng of large yellow croaker DNA in the PCR amplification reaction system of primer pair J2, filled up with double distilled water to 25ul, the primer sequence is
[0057] J1 upstream primer 5′-GGCATTTAGGCACAAGGAC-3′
[0058] J1 downstream primer 5′-GGGGGCACAACTCAGAGG-3′
[0059] J2 upstream primer 5′-CAGGCCCCACCATACTAGT-3′
[0060] J2 Downs...
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