Method for judging lateolabrax japonicus aquatic water
A technology for cultivating water bodies and perch, applied in the fields of biochemical equipment and methods, determination/inspection of microorganisms, etc.
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Embodiment 1
[0024] (1) Extraction of total RNA: Put 50 mg of the gill tissue of sea bass cultured in seawater into a mortar, add liquid nitrogen, and grind the tissue into powder after the liquid nitrogen volatilizes. Put the tissue powder into a 1.5ml centrifuge tube, add Trizol reagent (purchased from Invitrogen) to lyse for 5-10 minutes, then add chloroform and let stand at room temperature for 15 minutes, then centrifuge in a centrifuge for 15 minutes (12000 rpm), take 500ul of supernatant, add isopropanol and let it stand for 10min, then centrifuge for 10min (12000 rpm), pour off the supernatant, add 75% alcohol to wash the precipitate, after centrifugation, pour off the supernatant to obtain the gill tissue of sea bass cultured in seawater Total RNA, add 40 μl DEPC water to dissolve and set aside;
[0025] (2) Synthesis of the first strand of cDNA: using the M-MLV reverse transcriptase kit purchased from Promega. Take the extracted total RNA with a volume of more than 1 μl, mix it ...
Embodiment 2
[0030] The specific steps are the same as in Example 1, except that the tissue used is the kidney of sea bass cultured in seawater.
Embodiment 3
[0032] The specific steps are the same as in Example 1, except that the tissue used is the gills of freshwater cultured perch.
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