Quick sperm acrosin extraction method and sperm acrosin activity flow cytometry detection method
An extraction method and flow detection technology, which are applied in the field of rapid extraction method and flow detection of its activity, can solve the problems of difficult accurate quantification, low acrosome enzyme activity, and insufficient sensitivity, so as to achieve improved efficiency, mild treatment, The effect of simplifying the experimental operation steps
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specific Embodiment 1
[0031] A method for rapidly extracting sperm acrosome enzyme, comprising the following steps:
[0032] (1) will contain 7.5*10 6 Add the semen with the number of sperm into the centrifuge tube, centrifuge at 10000rpm for 2min, absorb the seminal plasma in the tube after centrifugation, and keep the lower layer of sperm sediment;
[0033] (2) Add 200uL permeabilization solution to the centrifuge tube containing the sperm pellet, suspend the sperm pellet evenly, centrifuge at 7000rpm for 2min, remove the supernatant, then add 400uL extract solution, suspend the sperm at 37°C for 10min, and then After centrifuging at 12000rpm for 3min, collect the supernatant to obtain the acrosome enzyme extract, which contains 1.2g sodium dihydrogen phosphate, 0.2-0.4ml Triton-1000. Contains 1g of BSA, 0.35g of sodium chloride, 1.19g of sodium monohydrogen phosphate, 0.25g of sodium dihydrogen phosphate dihydrate and 0.05g of sodium azide.
[0034] The extracted acrosome can be stored at -20°...
specific Embodiment 2
[0038] A method for flow detection of sperm acrosome activity, comprising the following steps:
[0039] (1) Collection of samples: After counting the freshly collected and completely liquefied sperm samples by a sperm counter, take 7.5*10 6 Centrifuge at 10,000rpm for 2min with the number of sperm, discard the supernatant with the tip of a pipette, and leave the sperm sample to precipitate for later use;
[0040] (2) Cell lysis: Add 200uL membrane-permeating solution to the sperm cell pellet obtained in step (1), blow the cells up and down with a pipette tip to fully resuspend the sperm cells, and centrifuge the resuspension at 7000rpm for 2-4min (not If it exceeds 5 minutes, otherwise it will affect the activity of acrosome enzyme), suck off the supernatant with the tip of the pipette, and leave the precipitate for later use; the formula of the rupture solution is: every 100ml of the membrane rupture solution contains 1.2g of sodium dihydrogen phosphate, Triton-1000.2 -0.4ml...
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