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用于神经组织细胞碱性和酸性蛋白质细胞分光光度法的一些组织化学显色反应分析。

Analysis of some histochemical colour reactions for cytospectrophotometry of basic and acidic proteins in nervous tissue cells.

作者信息

Brumberg V A, Pevzner L Z

出版信息

Microsc Acta. 1978 May;80(4):323-30.

PMID:79129
Abstract

Cytospectrophotometric analysis of model systems and of single cells in Carnoy-fixed paraffin sections of the nervous tissue has shown two histochemical colour reactions for basic proteins and two reactions for acidic proteins to obey Bouger-Lambert-Beer's law. Basic proteins can be stoichiometrically stained either with Fast Green FCF, pH 8.2, or with heparin-Alcian Blue; acidic proteins either with Fast Green, FCF, pH 2.6, or with Toluidine Blue o. basing on better reproducibility of cytochemical results and sufficiently good preservation of cell structure, heparine-Alcian Blue is recommended for cytospectrophotometric determinations of basic proteins. To stain acidic proteins both Fast Green, pH 2.6, and Toluidine Blue O are recommended, each of the dyes being characterized by its own advantages and disadvantages.

摘要

对模型系统以及经卡诺伊固定的神经组织石蜡切片中的单细胞进行细胞分光光度分析表明,碱性蛋白的两种组织化学显色反应以及酸性蛋白的两种反应均符合布格-朗伯-比尔定律。碱性蛋白可用pH 8.2的固绿FCF或肝素-阿尔辛蓝进行化学计量染色;酸性蛋白可用pH 2.6的固绿FCF或甲苯胺蓝O进行染色。基于细胞化学结果更好的可重复性以及细胞结构足够良好的保存情况,推荐使用肝素-阿尔辛蓝进行碱性蛋白的细胞分光光度测定。对于酸性蛋白的染色,推荐使用pH 2.6的固绿和甲苯胺蓝O,每种染料都有其自身的优缺点。

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