高尔基体
免疫荧光
荧光团
一级和二级抗体
共焦显微镜
荧光显微镜
抗体
荧光
细胞生物学
共焦
标签
显微镜
生物
化学
生物物理学
分子生物学
生物化学
病理
免疫学
内质网
光学
医学
物理
作者
M R Arab,Sanjeev Chavan Nayak,Teresa Vitali,Martin Lowe
出处
期刊:Methods in molecular biology
日期:2022-12-13
卷期号:: 101-111
标识
DOI:10.1007/978-1-0716-2639-9_8
摘要
Immunofluorescence is a technique that uses antibodies and fluorophores to label structures inside cells. The cells are normally fixed and permeabilized, and then structures are labelled using primary antibodies directly conjugated to fluorophores, or, more commonly, first with an antibody against an antigen of interest followed by a secondary antibody conjugated to a fluorophore that binds to the primary antibody. Fluorescence can be visualized using widefield, confocal, or super-resolution microscopy. Here we focus on labelling of the Golgi apparatus and show that different fixation and permeabilization conditions can significantly affect labelling of Golgi proteins and describe how to optimize fluorescent detection of Golgi proteins.
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