In-vitro culture system kit for improving sperm motility of human bodies and application method thereof
An in vitro culture system and sperm motility technology, which is applied in the field of culture system kits containing active recombinant proteins, can solve the problems of ineffective improvement of sperm motility, and achieve the goal of improving forward motility, pregnancy outcome, and fertilization rate Effect
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Embodiment 1
[0016] Sample source: three normal motility sperm samples (the standard is according to the fifth edition of WHO)
[0017] Sperm processing:
[0018] 1. Preheat 10mL of mHTF containing 10% SSS by volume (as a control group before culture), 2mL Isolate sperm separation solution and 10mL of the sperm culture system of the present invention.
[0019] 2. Place the semen collection cup in a 37°C water bath and take it out after liquefaction.
[0020] 3. Mix the preheated mHTF containing 10% SSS with the liquefied semen, slowly add it to the Isolate sperm separation medium, and centrifuge at 300g for 10 minutes.
[0021] 4. Discard the supernatant after centrifugation, remove the lower layer and separate the sperm for microscopic examination, record the sperm motility, and serve as the control group before culture.
[0022] 5. Mix the remaining sperm from step (4) with the sperm culture system of the present invention at a concentration of 10 million / mL, and place in a 37°C incuba...
Embodiment 2
[0026] Sample source: three sperm samples from patients with asthenozoospermia (the standard is according to the fifth edition of WHO)
[0027] Sperm processing:
[0028] 1. Preheat 10mL of mHTF containing 10% SSS by volume (as a control group before culture), 2mL of Isolate sperm separation solution and 10mL of the sperm culture system of the present invention.
[0029] 2. Place the semen collection cup in a 37°C water bath, and take it out after liquefaction.
[0030] 3. Mix the preheated mHTF with a volume fraction of 10% SSS and the liquefied semen, slowly add it to the Isolate separation solution, and centrifuge at 300g for 10 minutes.
[0031] 4. Discard the supernatant after centrifugation, remove the lower layer and separate the sperm for microscopic examination, record the sperm motility, and serve as the control group before culture.
[0032] 5. Mix the remaining sperm from step (4) with the sperm culture system of the present invention at a concentration of 10 mil...
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