A method for evaluating the release effect of Penaeus japonicus
A technology of prawns and objects, which is applied in the field of evaluation of the release effect of Penaeus japonica, can solve the problems of the inability to scientifically evaluate the level of supplementation of wild resources by the released population, and the inability to accurately distinguish the released individuals from the wild individuals and the number of recaptured groups, so as to promote The effect of population resource recovery, low cost and simple process
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[0025] DNA extraction and PCR from Penaeus japonicus:
[0026] (1) DNA extraction: Trizol method extraction.
[0027] A. Take 1000μL Tris-cl into a 2ml centrifuge tube;
[0028] B. Take an appropriate amount of tissue (about 2-3mg), and fully cut it with sterilized scissors;
[0029] C. After soaking for 45min, 4℃, 12000rpm, 10mim;
[0030] D. Discard the supernatant, add 600 μL Tris-buffer, 50 μL 10% SDS, 7 μL proteinase K, water bath at 55°C for 2 h, until complete digestion and the solution is clear;
[0031] E. Add 350 μL phenol, 350 μL chloroform:isoamyl alcohol (24:1), shake until completely mixed; 4°C, 12000rpm, 10mim;
[0032] F. Take the supernatant into a new 2ml centrifuge tube, add the same volume of chloroform:isoamyl alcohol (24:1) as the supernatant, shake until completely mixed; 4°C, 12000rpm, 10mim;
[0033] G. Take the supernatant into a new 1.5ml centrifuge tube, add 2 times the volume of supernatant with ice anhydrous ethanol, mix well, let stand at -20...
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