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用于电子显微镜的脂质染色:一种新方法。

Lipid staining for the electron microscope: a new method.

作者信息

Wigglesworth V B

出版信息

J Cell Sci. 1975 Dec;19(3):425-37. doi: 10.1242/jcs.19.3.425.

Abstract

Tissues fixed in osmium tetroxide or in combined osmium and glutaraldehyde (Hinde), embedded in Spurr's medium, cut at 0-5-I mum and mounted in Farrants' gum medium containing ethyl gallate, show good staining of lipid-contaning structures (droplets of triglyceride, membranes, mitochondria, etc.) in the light microscope. Such preparations show moderate contrast in the electron microscope without further staining. But a specific increase in contrast in lipid-rich structures is obtained by partition of the tissues, before embedding, in 70% ethanol saturated with the monoterpene hydrocarbon myrcene, with or without the addition of 0-I % ethyl gallate, followed by osmium tetroxide. This method will visualize both saturated and unsaturated lipids, including waxes.

摘要

用四氧化锇或锇与戊二醛混合液(欣德法)固定、包埋于斯珀树脂介质中、切成0.5 - 1微米厚并置于含没食子酸乙酯的法伦特树胶介质中的组织,在光学显微镜下显示出含脂结构(甘油三酯滴、膜、线粒体等)的良好染色。此类标本在电子显微镜下无需进一步染色就有适度的反差。但是,在包埋前,将组织置于用单萜烃月桂烯饱和的70%乙醇中(添加或不添加0.1%没食子酸乙酯),然后用四氧化锇处理,可使富含脂质的结构的反差显著增加。该方法能使包括蜡质在内的饱和及不饱和脂质都显现出来。

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