细胞质
微管蛋白
微管
细胞骨架
膜
荧光显微镜
细胞生物学
试剂
肌动蛋白
生物物理学
麦胚凝集素
细胞
化学
生物
荧光
生物化学
凝集素
物理化学
物理
量子力学
作者
O. J. Golub,Jason A. Kilgore,Nick J. Dolman
摘要
Abstract Non‐antibody commercial fluorescent reagents for imaging of cytoskeletal structures have been limited primarily to labeling tubulin and actin, with the key factor in choice based mainly on whether cells are live or fixed and permeabilized. A wider range of options exists for cell membrane dyes, and the choice of reagent primarily depends on the preferred localization in the cell (i.e., all membranes or only the plasma membrane) and usage (i.e., whether the protocol involves fixation and permeabilization). For whole‐cell or cytoplasmic imaging, the choice of reagent is determined mostly by the length of time that the cells need to be visualized (hours or days) and by fixation status. Presented here is a discussion on choosing commercially available reagents for labeling these cellular structures, with an emphasis on use for microscopic imaging, with a featured reagent, recommended protocol, troubleshooting guide, and example image for each structure. © 2023 Wiley Periodicals LLC. Basic Protocol 1 : Actin labeling Basic Protocol 2 : Wheat germ agglutinin conjugates for plasma membrane labeling Basic Protocol 3 : Labeling tubulin microtubules with Tubulin Tracker Deep Red Basic Protocol 4 : Labeling whole cells or cytoplasm with 5(6)‐CFDA SE
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