Preparation method of agonist for improving stock boar sperm activity
A sperm motility and agonist technology, applied in biochemical equipment and methods, cell culture active agents, preservation of human or animal bodies, etc., can solve the problem of limited boar sperm motility, the influence of boar sperm production years, boar boar Testicular atrophy and other problems, to achieve the effect of easy promotion and use, easy processing and production, and little toxic effect
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Embodiment 1
[0034] A preparation method for improving boar sperm motility agonist,
[0035] Prepared by:
[0036] (1) Take out the boar testis tissue and soak it in 37°C normal saline with 1% double antibody for 10-30min;
[0037] (2) Take out the infiltrated boar testis tissue and wash it three times with PBS buffer containing 1% double antibody;
[0038] (3) Add DMEM / F12 cell culture medium, incubate at 37°C for 30 minutes, fully decompose the testicular tissue, transfer the dispersed tissue fluid to a centrifuge tube, and centrifuge to remove the supernatant;
[0039] (4) Add 1.5mL of hyaluronidase and 1.5mL of collagenase IV into the centrifuge tube, shake vigorously every 2 minutes at 37°C, after 2-3 times of continuous shaking, add 3mL of DMEM / F12 cell culture solution, centrifuged to remove the supernatant;
[0040] (5) Add 1.5mL trypsin and 1.5mL deoxyribonuclease into the centrifuge tube, shake vigorously every 2 minutes at 37°C, and after shaking continuously for 2-3 times, a...
Embodiment 2
[0046] A preparation method for improving boar sperm motility agonist, characterized in comprising the following steps:
[0047] (1) Take out the boar testis tissue and soak it in 37°C normal saline with 1% double antibody for 10-30min;
[0048] (2) Take out the infiltrated boar testis tissue and wash it three times with PBS buffer containing 1% double antibody;
[0049] (3) Add DMEM / F12 cell culture medium, incubate at 37°C for 30 minutes, fully decompose the testicular tissue, transfer the dispersed tissue fluid to a centrifuge tube, and centrifuge to remove the supernatant;
[0050] (4) Add 1.5mL of hyaluronidase and 1.5mL of collagenase IV into the centrifuge tube, shake vigorously every 2 minutes at 37°C, after 2-3 times of continuous shaking, add 3mL of DMEM / F12 cell culture solution, centrifuged to remove the supernatant;
[0051] (5) Add 1.5mL trypsin and 1.5mL deoxyribonuclease into the centrifuge tube, shake vigorously every 2 minutes at 37°C, and after shaking con...
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