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一种用于在电子显微镜下快速显示组织抗原的简易包埋后系统。

A simple post-embedding system for the rapid demonstration of tissue antigens under the electron microscope.

作者信息

Newman G R, Jasani B, Williams E D

出版信息

Histochem J. 1983 Jun;15(6):543-55. doi: 10.1007/BF01954145.

Abstract

A simple and versatile technique for the preparation of ultra-thin sections, which can be stained immunohistochemically directly on electron microscope grids, is presented. An anti-hapten immunoperoxidase procedure has been adapted for use on tissue fixed in a purified monomeric glutaraldehyde--picric acid mixture, and embedded in 'L R White', a recently formulated plastic resin. This plastic tolerates the use of partial dehydration of tissue, resulting in higher antigenic yields. In addition, no etching of ultra-thin sections is necessary, and the whole immunostaining procedure can be completed in less than 2 h. A comparison of commonly used fixatives is discussed. High-resolution micrographs showing general staining (uranyl acetate--lead citrate) of rat pancreas, and immunostaining of insulin and TSH in storage granules in perfusion-fixed rat tissue and of lambda-chain immunoreactive cells in immersion-fixed human tonsil are included as examples.

摘要

本文介绍了一种简单通用的超薄切片制备技术,该切片可直接在电子显微镜网格上进行免疫组织化学染色。一种抗半抗原免疫过氧化物酶方法已适用于固定在纯化单体戊二醛 - 苦味酸混合物中,并包埋于“LR White”(一种新配制的塑料树脂)中的组织。这种塑料允许对组织进行部分脱水处理,从而提高抗原产量。此外,无需对超薄切片进行蚀刻,整个免疫染色过程可在不到2小时内完成。文中讨论了常用固定剂的比较。还包括高分辨率显微照片作为示例,展示了大鼠胰腺的常规染色(醋酸铀 - 柠檬酸铅),灌注固定大鼠组织中储存颗粒内胰岛素和促甲状腺激素的免疫染色,以及浸泡固定人扁桃体中λ链免疫反应性细胞的免疫染色。

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