{"title":"Immunofluorescence Microscopy","authors":"David J. Asai","doi":"10.1002/9780470089941.et0902s10","DOIUrl":null,"url":null,"abstract":"<p>The visualization of fluorescently tagged molecules is a powerful strategy that can contribute to the understanding of the complex dynamics of the cell. A particularly robust and broadly applicable method is immunofluorescence microscopy, in which a specific fluorescently labeled antibody binds the molecule of interest and then the location of the antibody is determined by fluorescence microscopy. The effective application of this technique includes several considerations, including the nature of the antigen, specificity of the antibody, permeabilization and fixation of the specimen, and fluorescence imaging of the cell. Although each protocol will require fine-tuning depending on the cell type, the antibody, and the antigen, there are steps common to nearly all applications. This unit provides protocols for visualization of the cytoskeleton in two very different kinds of cells: flat, adherent fibroblasts and thick, free-swimming <i>Tetrahymena</i> cells. © 2015 by John Wiley & Sons, Inc.</p>","PeriodicalId":500994,"journal":{"name":"Current Protocols Essential Laboratory Techniques","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/9780470089941.et0902s10","citationCount":"115","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols Essential Laboratory Techniques","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/9780470089941.et0902s10","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 115
Abstract
The visualization of fluorescently tagged molecules is a powerful strategy that can contribute to the understanding of the complex dynamics of the cell. A particularly robust and broadly applicable method is immunofluorescence microscopy, in which a specific fluorescently labeled antibody binds the molecule of interest and then the location of the antibody is determined by fluorescence microscopy. The effective application of this technique includes several considerations, including the nature of the antigen, specificity of the antibody, permeabilization and fixation of the specimen, and fluorescence imaging of the cell. Although each protocol will require fine-tuning depending on the cell type, the antibody, and the antigen, there are steps common to nearly all applications. This unit provides protocols for visualization of the cytoskeleton in two very different kinds of cells: flat, adherent fibroblasts and thick, free-swimming Tetrahymena cells. © 2015 by John Wiley & Sons, Inc.
免疫荧光显微镜
荧光标记分子的可视化是一种强大的策略,可以有助于理解细胞的复杂动力学。一种特别强大和广泛适用的方法是免疫荧光显微镜,其中一种特定的荧光标记抗体结合感兴趣的分子,然后通过荧光显微镜确定抗体的位置。该技术的有效应用包括几个考虑因素,包括抗原的性质,抗体的特异性,标本的渗透和固定,以及细胞的荧光成像。尽管每个方案都需要根据细胞类型、抗体和抗原进行微调,但几乎所有的应用都有共同的步骤。该单元提供了两种非常不同类型细胞的细胞骨架可视化方案:扁平、贴壁的成纤维细胞和厚的、自由游动的四膜细胞。©2015 by John Wiley &儿子,Inc。
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