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通过精子活力生物测定法监测储存培养基的变质情况。

Deterioration of stored culture media as monitored by a sperm motility bioassay.

作者信息

Stewart-Savage J, Bavister B D

机构信息

Department of Veterinary Science, University of Wisconsin, Madison 53706.

出版信息

J In Vitro Fert Embryo Transf. 1988 Apr;5(2):76-80. doi: 10.1007/BF01130662.

Abstract

A hamster sperm motility bioassay was used to monitor medium quality during storage. The media studied were (1) TL-PVA, a modified Tyrode's solution; (2) TLP-PVA, a defined medium that supports hamster sperm motility but does not support capacitation; and (3) TALP-PVA (TLP-PVA + serum albumin), which supports hamster sperm survival and capacitation. Each medium was stored at 5 and -20 degrees C and tested every two weeks. All of the media deteriorated with increased storage time, but at different rates (TLP-PVA greater than TL-PVA greater than TALP-PVA). The deterioration of the media correlated with an increase in pH during storage, probably due to a loss of CO2 and bicarbonate. Albumin, added after storage, was able to rescue frozen TL-PVA.

摘要

采用仓鼠精子活力生物测定法对储存期间的培养基质量进行监测。所研究的培养基有:(1)TL - PVA,一种改良的Tyrode氏溶液;(2)TLP - PVA,一种能支持仓鼠精子活力但不支持获能的限定培养基;(3)TALP - PVA(TLP - PVA + 血清白蛋白),能支持仓鼠精子存活和获能。每种培养基分别储存在5℃和 - 20℃,每两周进行一次测试。所有培养基均随储存时间延长而变质,但速率不同(TLP - PVA > TL - PVA > TALP - PVA)。培养基的变质与储存期间pH值升高相关,这可能是由于二氧化碳和碳酸氢盐的损失所致。储存后添加白蛋白能够挽救冷冻的TL - PVA。

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