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旧的不去,新的不来:用于切片生物材料电子显微镜检查的快速标本制备程序。

Out with the old and in with the new: rapid specimen preparation procedures for electron microscopy of sectioned biological material.

作者信息

McDonald Kent L

机构信息

Electron Microscope Laboratory, University of California, 26 Giannini Hall, Berkeley, CA, 94720, USA,

出版信息

Protoplasma. 2014 Mar;251(2):429-48. doi: 10.1007/s00709-013-0575-y. Epub 2013 Nov 21.

Abstract

This article presents the best current practices for preparation of biological samples for examination as thin sections in an electron microscope. The historical development of fixation, dehydration, and embedding procedures for biological materials are reviewed for both conventional and low temperature methods. Conventional procedures for processing cells and tissues are usually done over days and often produce distortions, extractions, and other artifacts that are not acceptable for today's structural biology standards. High-pressure freezing and freeze substitution can minimize some of these artifacts. New methods that reduce the times for freeze substitution and resin embedding to a few hours are discussed as well as a new rapid room temperature method for preparing cells for on-section immunolabeling without the use of aldehyde fixatives.

摘要

本文介绍了制备用于电子显微镜薄切片检查的生物样品的当前最佳实践方法。回顾了生物材料固定、脱水和包埋程序的历史发展,包括传统方法和低温方法。处理细胞和组织的传统程序通常需要数天时间,并且常常会产生变形、提取和其他伪像,这些对于当今的结构生物学标准来说是不可接受的。高压冷冻和冷冻置换可以将其中一些伪像降至最低。还讨论了将冷冻置换和树脂包埋时间缩短至数小时的新方法,以及一种无需使用醛类固定剂即可快速在室温下制备细胞用于切片后免疫标记的新方法。

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