Preparation method of agonist for improving fish sperm motility
A fish sperm and agonist technology, applied in biochemical equipment and methods, cell culture active agents, animal cells, etc., can solve the problems of not being fully utilized, and achieve the goal of easy popularization, use, and production Effect
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Embodiment 1
[0034] A preparation method for improving fish sperm motility agonist,
[0035] Prepared by:
[0036] (1) Take gonads of Atlantic salmon whose gonads are in the V stage of development, and put them into Hanks solution at 28°C with 2% penicillin for 45 minutes;
[0037] (2) Isolate the mesenchymal cells of Atlantic salmon gonads, and wash them twice with Hanks solution containing 2% streptomycin;
[0038] (3) Add HHBS cell culture medium, incubate at 28°C for three days, and subculture according to the growth state of the cells at a ratio of 1:2 or 1:3, transfer the subcultured cell liquid to a centrifuge tube, and centrifuge remove the supernatant;
[0039] (4) Add 3 mL of hyaluronidase into the centrifuge tube, shake vigorously every 2 minutes at 28°C, and after shaking continuously for 4 to 5 times, add 5 mL of cell culture medium, and take the cultured cell liquid at 2000r / min Centrifuge to remove the supernatant. ;
[0040] (5) filter the supernatant with a cell sieve...
Embodiment 2
[0043] A preparation method for improving fish sperm motility agonist is characterized in that it comprises the following steps:
[0044] (1) Take the gonads of turbot whose gonads are in the V stage of development, and soak them in 28°C Hanks solution with 2% penicillin for 45 minutes;
[0045] (2) Separating the interstitial cells of turbot gonads and washing them twice with Hanks solution containing 2% streptomycin;
[0046] (3) Add HHBS cell culture medium, incubate at 28°C for three days, and subculture according to the growth state of the cells at a ratio of 1:2 or 1:3, transfer the subcultured cell liquid to a centrifuge tube, and centrifuge remove the supernatant;
[0047] (4) Add 3 mL of hyaluronidase into the centrifuge tube, shake vigorously every 2 minutes at 28°C, and after shaking continuously for 4 to 5 times, add 5 mL of cell culture medium, and take the cultured cell liquid at 2000r / min Centrifuge to remove the supernatant. ;
[0048] (5) filter the supernat...
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