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一种从啮齿动物附睾头和兔射精后精浆中分离精子头部的简化方法。

A simplified method for the isolation of sperm heads from the caput epididymidis of rodents and from ejaculated rabbit seminal plasma.

作者信息

Lee I P, Schmid B, Zbinden G

出版信息

Exp Cell Biol. 1977;45(1-2):48-59. doi: 10.1159/000162857.

Abstract

The present report describes a simple and rapid procedure to isolate highly purified sperm heads from mouse, rat and rabbit. The isolation procedure involves mincing of the caput epididymidis (CPE) of mice and rats to obtain a crude CPE suspension. This suspension is filtered to remove tubular fragments. The filtrate containing sperms and cellular contaminants is trypsinized, followed by sonication. To obtain rabbit sperm head suspension, ejaculated spermatozoa are briefly exposed to the cationic detergent CTAB-D, followed by trypsinization. Trypsin treatment of the suspension yields sperm heads and tails. The suspension containing sperm heads and tails is separated by discontinuous sucrose density gradient centrifugation. Highly purified and enriched sperm heads are recovered from the bottom of 2.5 M sucrose of the gradient. Enriched sperm heads contain less than 1% sperm tails.

摘要

本报告描述了一种从小鼠、大鼠和兔子中分离高度纯化精子头部的简单快速方法。分离过程包括将小鼠和大鼠的附睾头(CPE)切碎以获得粗制的CPE悬浮液。该悬浮液经过过滤以去除管状碎片。含有精子和细胞污染物的滤液用胰蛋白酶处理,然后进行超声处理。为了获得兔精子头部悬浮液,将射出的精子短暂暴露于阳离子去污剂CTAB-D,然后进行胰蛋白酶处理。对悬浮液进行胰蛋白酶处理可产生精子头部和尾部。含有精子头部和尾部的悬浮液通过不连续蔗糖密度梯度离心进行分离。从梯度的2.5M蔗糖底部回收高度纯化和富集的精子头部。富集的精子头部含有少于1%的精子尾部。

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