发布: 2016年07月05日第6卷第13期 DOI: 10.21769/BioProtoc.1864 浏览次数: 12346
评审: Maria SinetovaCindy AstAnonymous reviewer(s)
Abstract
Determining the protein localization is essential to elucidate its in vivo function. Fluorescence-tagged proteins are widely used for it, but it is sometimes difficult to express tagged proteins in Chlamydomonas. Alternatively, indirect immunofluorescence assay is also one of the widely used methods and many reports determining the localization of Chlamydomonas proteins using this method are published. Here, we introduce a protocol of indirect immunofluorescence assay adapted from our papers reporting LCIB (CO2-recycling factor in the vicinity of pyrenoid; Yamano et al., 2010), LCI1 (plasma membrane-localized inorganic carbon transporter; Ohnishi et al., 2010), HLA3 (plasma membrane-localized ABC-type bicarbonate transporter; Yamano et al., 2015), and LCIA (chloroplast envelope anion channel; Yamano et al., 2015) in Chlamydomonas reinhardtii. The protocol described here could be useful for observing the protein of interest in other algae cells.
Keywords: Chloroplast membrane (叶绿体膜)Materials and Reagents
Equipment
Note: these were the instruments used throughout our experiments, but any company is OK.
Procedure
文章信息
版权信息
© 2016 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Yamano, T. and Fukuzawa, H. (2016). Indirect Immunofluorescence Assay in Chlamydomonas reinhardtii. Bio-protocol 6(13): e1864. DOI: 10.21769/BioProtoc.1864.
分类
植物科学 > 植物生物化学 > 蛋白质
生物化学 > 蛋白质 > 免疫检测
细胞生物学 > 细胞成像 > 荧光
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