Torres Nikko P, Brown Grant W
Department of Biochemistry and Donnelly Centre, University of Toronto, 160 College Street, Toronto, ON, Canada, M5S 3E1.
Methods Mol Biol. 2015;1300:1-12. doi: 10.1007/978-1-4939-2596-4_1.
High-throughput imaging of yeast cells expressing fluorescent proteins can be used to understand biological pathways in the context of spatial organization. Here we describe a method for imaging yeast cells expressing proteins tagged with green fluorescent protein (GFP) and/or red fluorescent protein (RFP), with or without drug treatment, in a 384-well format, using the PerkinElmer Opera high-content confocal imaging microscope.
对表达荧光蛋白的酵母细胞进行高通量成像,可用于在空间组织背景下理解生物途径。在此,我们描述一种方法,使用珀金埃尔默Opera高内涵共聚焦成像显微镜,以384孔板形式对表达用绿色荧光蛋白(GFP)和/或红色荧光蛋白(RFP)标记的蛋白质的酵母细胞进行成像,无论是否经过药物处理。