hybrid yellow catfish ch 4 Enzyme digestion method
An enzyme digestion identification, yellow catfish technology, applied in biochemical equipment and methods, microbial determination/inspection and other directions, can solve the problems affecting popularization, low detection efficiency, low repeatability, etc., to achieve intuitive identification and easy operation. , the effect of fast experiment
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Embodiment 1
[0028] CH 4 Enzyme digestion identification method, using CH after PCR amplification 4 There are interspecies sequence differences between the gene fragments of Pedelvis catfish and P. Pelvic catfish and its hybrid offspring.
Embodiment 2
[0030] CH 4 Enzyme digestion identification method specifically comprises the following steps:
[0031] A, take the tissue sample of the fish to be tested, and extract the genomic DNA;
[0032] B. Using the extracted genomic DNA as a template, carry out PCR amplification under the guidance of special primers;
[0033] C. Digest the amplified target gene fragment with restriction endonuclease HindⅢ, and the restriction site is A↓AGCTT;
[0034] D. PCR-RFLP product was detected by agarose gel electrophoresis. After electrophoresis detection, there was only one band on the same swimming lane, which was Peeled catfish; there were two bands on the same swimming lane, which was Peeled catfish; in the same swimming lane There are three bands on it, which is a hybrid.
Embodiment 3
[0036] CH 4 Enzyme digestion identification method specifically comprises the following steps:
[0037] A, take the tissue sample of the fish to be tested, and extract the genomic DNA;
[0038] B. Using the extracted genomic DNA as a template, carry out PCR amplification under the guidance of special primers;
[0039] C. Digest the amplified target gene fragment with restriction endonuclease HindⅢ, and the restriction site is A↓AGCTT;
[0040] D. The PCR-RFLP product was detected by agarose gel electrophoresis. After electrophoresis detection, there was only one band on the same swimming lane, which was peltatus varschii.
[0041] The special primer in the B step is CH 4Specific primers for gene fragments, the primer pair is:
[0042] Forward primer 5'-TCCCCAAGGTTTACTTGCTCGCTCC-3';
[0043] Reverse primer 5'-CGATGGATCTGGATATGTGGCGCAC-3'.
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