In vitro culture system kit for raising human sperm motility and application thereof
A technology for in vitro culture and sperm motility, applied in the field of XX, can solve the problem of insignificant improvement of sperm motility, and achieve the effects of improving forward motility, improving pregnancy outcome, and improving fertilization rate.
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Embodiment 1
[0023] Sample source: Three normal motility sperm specimens (standard according to the fifth edition of WHO)
[0024] Sperm processing:
[0025] 1. Preheat 10 mL of mHTF with a volume fraction of 10% SSS (as a pre-culture control group), 2 mL of LIsolate sperm separation solution and 10 mL of the in vitro culture solution of the present invention.
[0026] 2. Place the semen collection cup with the semen in a 37°C water bath and take it out after liquefaction.
[0027] 3. Mix the preheated mHTF containing 10% SSS with the liquefied semen, slowly add it to the Isolate sperm separation solution, and centrifuge at 300g for 10 minutes.
[0028] 4. After centrifugation, the supernatant was discarded, the lower layer was separated and the sperm was examined under a microscope, and the sperm motility was recorded as the control group before culture.
[0029] 5. Mix the remaining sperm of step 4 with the sperm in vitro culture solution of the present invention at a concentration of 10 million / ml...
Embodiment 2
[0033] Sample source: three sperm specimens of asthenospermia patients (standard according to the fifth edition of WHO)
[0034] Sperm processing:
[0035] 1. Preheat 10 mL of mHTF with a volume fraction of 10% SSS (as a pre-culture control group), 2 mL of LIsolate sperm separation solution and 10 mL of the in vitro culture solution of the present invention.
[0036] 2. Place the semen collection cup with the semen in a 37°C water bath and take it out after liquefaction.
[0037] 3. Mix the preheated mHTF containing 10% SSS with the liquefied semen, slowly add it to the Isolate separation solution, and centrifuge at 300g for 10 minutes.
[0038] 4. After centrifugation, the supernatant was discarded, the lower layer was separated and the sperm was examined under a microscope, and the sperm motility was recorded as the control group before culture.
[0039] 5. Mix the remaining sperm of step 4 with the sperm culture system of the present invention at a concentration of 10 million / ml, and ...
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