Sheep semen dilution preserving fluid and preparation method thereof
A technology for preserving liquid and semen, applied in the field of animal reproduction, can solve problems such as reduction and unsatisfactory acrosome integrity rate, and achieve the effects of simple production method, slowing sperm death, and reducing disease infection and spread.
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Embodiment 1
[0030] Sodium citrate 1.4g; fructose 2.0g; glucose 0.55g; D-galactose 0.45g; L-lysine 1.25g; fresh egg yolk centrifugal supernatant 15ml; sodium selenite 5.0mg; Sterilized double distilled water 100.0ml.
Embodiment 2
[0032] Sodium citrate 1.2g; fructose 1.8g; glucose 0.35g; D-galactose 0.25g; L-lysine 1.0g; fresh egg yolk centrifugal supernatant 12ml; sodium selenite 3.0mg; Sterilized double distilled water 100.0ml.
Embodiment 3
[0034] Sodium citrate 2.0g; fructose 2.5g; glucose 0.6g; D-galactose 0.5g; L-lysine 1.3g; fresh yolk centrifugal supernatant 20ml; sodium selenite 6.0mg; α-tocopherol 180IU; Sterilized double distilled water 100.0ml.
[0035] The sodium citrate described in the three embodiments is sodium citrate dihydrate, and its molecular formula is C 6 h 5 Na 3 o 7 2H 2 O.
[0036] combine figure 1 It can be seen that the specific production method of embodiment 1 is:
[0037] Make double distilled water first, measure 100.0ml of double distilled water, and autoclave at 110°C for 10 minutes to obtain sterilized double distilled water A. Accurately weigh 1.4g of sodium citrate, 0.55g of glucose, 0.45g of D-galactose, and 1.25g of L-lysine, respectively add them to sterilized double distilled water A, heat in a water bath at 50-60°C, and carry out sequential Stir clockwise to dissolve for 5-10 minutes, then autoclave at 110°C for 10 minutes to obtain solution B. Aseptically draw fre...
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