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一种获取包埋于聚乙二醇中的小组织标本0.5微米切片的简化方法。

A simplified method for obtaining 0.5-microns sections of small tissue specimens embedded in PEG.

作者信息

Holtham K A, Slepecky N B

机构信息

Department of Bioengineering and Neuroscience, Syracuse University, New York, USA.

出版信息

J Histochem Cytochem. 1995 Jun;43(6):637-43. doi: 10.1177/43.6.7769235.

Abstract

We describe a new method for embedding small specimens in polyethylene glycol (PEG) 4000. This method preserves cell morphology and provides sensitive immunocytochemical labeling with excellent subcellular resolution. Small tissues are embedded in agarose so that they can be grouped together and oriented for sectioning before infiltration with PEG 4000, a water-soluble polymer. Fixation, embedding, sectioning, and staining can be performed in 1 day. Results from immunocytochemical studies localizing actin and tubulin on 0.5-micron sections of PEG-embedded specimens are compared with those obtained on semi-thin sections of araldite-embedded specimens and demonstrate the ease, speed, and increased sensitivity of this embedding method.

摘要

我们描述了一种将小标本包埋于聚乙二醇(PEG)4000中的新方法。该方法可保存细胞形态,并能提供具有出色亚细胞分辨率的灵敏免疫细胞化学标记。小组织先包埋于琼脂糖中,以便在用水溶性聚合物PEG 4000渗透之前将它们聚集在一起并定向切片。固定、包埋、切片和染色可在1天内完成。将在PEG包埋标本的0.5微米切片上定位肌动蛋白和微管蛋白的免疫细胞化学研究结果,与在环氧树脂包埋标本的半薄切片上获得的结果进行比较,证明了这种包埋方法的简便、快速和更高的灵敏度。

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