Scylla paramamosain biomarker CYP2 gene and application of scylla paramamosain biomarker CYP2 gene in preparation of pathological detection reagent
A technology of biological markers and pseudo-cave blue crabs, which is applied in the fields of plant gene improvement, biochemical equipment and methods, and microbial measurement/inspection, can solve the problems that hinder the healthy development of the blue crab industry, the low output per mu of blue crabs, and the Crab disease outbreaks and other issues
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[0021] 1. Materials method
[0022] 1.1 RNA extraction and cDNA synthesis
[0023] Total RNA was extracted from the hepatopancreas of Scylla simulans by sampling Trizol.
[0024] (1) Take 0.1 mg of hepatopancreas tissue for grinding, add 1 ml of Trizol, and let stand on ice for 10 min;
[0025] (2) Centrifuge at 12,000rpm for 5min, take the supernatant, add 200ul chloroform, shake vigorously, and let stand on ice for 5min;
[0026] (3) Centrifuge at 12,000 rpm for 5 min, absorb the upper aqueous phase, add an equal volume of isopropanol, and let stand on ice for 5-10 min;
[0027] (4) Centrifuge at 12,000rpm for 5min, discard the supernatant, add 1ml of 75% alcohol, and let stand on ice for 5-10min;
[0028] (5) Centrifuge at 8,000g for 5min, discard the supernatant, and dry at room temperature;
[0029] (6) Add 50ul DEPC water to dissolve.
[0030] The extracted RNA was measured by spectrophotometer, and the quality of RNA was detected by agarose gel electrophoresis. Qu...
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