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长时间四氧化锇固定后超声微切割:一种用于扫描电子显微镜的技术。

Microdissection by ultrasonication after prolonged OsO4 fixation: a technique for scanning electron microscopy.

作者信息

Highison G J, Low F N

出版信息

J Submicrosc Cytol. 1982 Jan;14(1):161-70.

PMID:7108993
Abstract

A new method of tissue preparation for electron microscopy is described for the selective dissection of mammalian tissues. This technique, based upon brittlization by prolonged osmication, dehydration to pure acetone and subsequent ultrasonication, has been especially useful for the SEM visualization of microcirculation and basal laminas. Epithelial cells of treated tissues were largely fragmented and removed, whereas collagen containing materials, notably epithelial and vascular basal laminas, withstood the vibratory insult. The extent of epithelium and basal lamina removal depended upon tissue type and duration of ultrasonic treatment. Alone or in conjunction with specific enzymatic pretreatment, this new technique offers a method to better visualize known and unrecognized histological relationships.

摘要

本文描述了一种用于电子显微镜检查的组织制备新方法,用于选择性解剖哺乳动物组织。该技术基于长时间锇酸处理使组织变脆、脱水至纯丙酮并随后进行超声处理,对于微循环和基膜的扫描电子显微镜观察特别有用。经处理的组织上皮细胞大部分破碎并被去除,而含胶原蛋白的物质,尤其是上皮和血管基膜,能够承受振动损伤。上皮和基膜的去除程度取决于组织类型和超声处理时间。单独使用或与特定酶预处理结合使用,这种新技术提供了一种更好地观察已知和未知组织学关系的方法。

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