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用聚腺苷酸核苷酸转移酶孵育超薄切片后对RNA进行免疫检测。

Immunodetection of RNA on ultra-thin sections incubated with polyadenylate nucleotidyl transferase.

作者信息

Thiry M

机构信息

Laboratory of Cellular and Tissular Biology, University of Liège, Pitteurs, Belgium.

出版信息

J Histochem Cytochem. 1993 May;41(5):657-65. doi: 10.1177/41.5.7682229.

Abstract

A new method is described for locating RNA on ultra-thin sections. Sections of aldehyde-fixed, plastic-embedded cells were incubated in a medium containing polyadenylate nucleotidyl transferase (PnT) and biotinylated ATP. The labeled nucleotides bound to RNA at the surface of the ultra-thin sections were than visualized by an indirect immunogold labeling technique. The resulting labeling pattern was dependent on the presence of divalent cations in the PnT medium. The method revealed with great precision the specific RNA-containing structures within Ehrlich tumor cells. The method is applicable to Epon sections. However, the labeling intensity varies according to the fixation used. Best results were obtained on acetylated cell sections. The method can be combined with EDTA regressive staining. The in situ PnT method provides a very useful tool for pinpointing the precise location of RNA within biological material at the ultrastructural level.

摘要

本文描述了一种在超薄切片上定位RNA的新方法。将醛固定、塑料包埋细胞的切片在含有聚腺苷酸核苷酸转移酶(PnT)和生物素化ATP的培养基中孵育。然后通过间接免疫金标记技术观察结合在超薄切片表面RNA上的标记核苷酸。产生的标记模式取决于PnT培养基中是否存在二价阳离子。该方法极其精确地揭示了艾氏瘤细胞内特定的含RNA结构。该方法适用于环氧树脂切片。然而,标记强度会因所用固定方法的不同而有所变化。在乙酰化细胞切片上获得了最佳结果。该方法可与EDTA回归染色相结合。原位PnT方法为在超微结构水平上精确确定生物材料中RNA的位置提供了一个非常有用的工具。

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