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培养的哺乳动物细胞的线粒体:I. 通过免疫荧光显微镜、组织化学、亚细胞分级分离和细胞融合进行分析

The mitochondria of cultured mammalian cells: I. Analysis by immunofluorescence microscopy, histochemistry, subcellular fractionation, and cell fusion.

作者信息

Malka Florence, Auré Karine, Goffart Steffi, Spelbrink Johannes N, Rojo Manuel

机构信息

INSERM U582-Institut de Myologie, Université Pierre et Marie Curie, IFR14, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

出版信息

Methods Mol Biol. 2007;372:3-16. doi: 10.1007/978-1-59745-365-3_1.

Abstract

Mitochondria form a dynamic network in which continuous movement, fusion, and division ensure the distribution and exchange of proteins and deoxyribonucleic acid (DNA). The recent past has seen the identification and characterization of the first proteins governing the organization, function, and dynamics of mitochondria and mitochondrial DNA, and it is predictable that numerous new proteins will require localization and functional characterization in the future. In this chapter, we describe methods for the visualization of mitochondria and mitochondrial activity in cultured mammalian cells to establish the localization or distribution of its components and to study mitochondrial fusion.

摘要

线粒体形成一个动态网络,其中持续的移动、融合和分裂确保了蛋白质和脱氧核糖核酸(DNA)的分布与交换。近年来,已鉴定并表征了首批控制线粒体及线粒体DNA的组织、功能和动态的蛋白质,并且可以预见,未来还会有大量新蛋白质需要进行定位和功能表征。在本章中,我们描述了用于观察培养的哺乳动物细胞中线粒体及线粒体活性的方法,以确定其组分的定位或分布,并研究线粒体融合。

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