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[使用生物素化探针通过原位杂交在培养动物细胞超薄切片上进行核糖体RNA的超微结构检测]

[Ultrastructural detection of ribosomal RNA by in situ hybridization using a biotinylated probe on ultrathin sections of cultured animal cells].

作者信息

Escaig-Haye F, Grigoriev V, Fournier J G

机构信息

Hôpital Saint-Vincent-de-Paul, I.N.S.E.R.M., U. n 43, Paris.

出版信息

C R Acad Sci III. 1989;309(10):429-34.

PMID:2514968
Abstract

A genomic probe containing ribosomal sequences and labelled with biotin was used to hybridize rRNA molecules in ultrathin sections of animal cells embedded in Lowicryl K4M. After detection with streptavidin conjugated with 10 nm gold particles, ribosomal target sequences were localized preferentially in the dense fibrillar component of the nucleolus and in the polyribosome structures of the cytoplasm. The method presently described offers the possibility to detect rapidly and precisely ribosomal gene expression at the ultrastructural level, particularly under different physiological and pathological conditions.

摘要

一个含有核糖体序列并标记有生物素的基因组探针,用于与包埋在Lowicryl K4M中的动物细胞超薄切片中的rRNA分子杂交。在用与10纳米金颗粒偶联的链霉亲和素检测后,核糖体靶序列优先定位在核仁的致密纤维成分和细胞质的多核糖体结构中。目前描述的方法提供了在超微结构水平上快速准确地检测核糖体基因表达的可能性,特别是在不同的生理和病理条件下。

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