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兔气管上皮培养物纤毛中微管蛋白与胶体金的免疫细胞化学定位

Immunocytochemical localization of tubulin with colloidal gold in cilia of rabbit tracheal epithelial cultures.

作者信息

Moller P C, Chang J P, Partridge L R

出版信息

Tissue Cell. 1983;15(1):39-45. doi: 10.1016/0040-8166(83)90032-0.

Abstract

Ciliated tracheal epithelia cell cultures were investigated immunocytochemically with anti-tubulin and colloidal gold. When rabbit tracheal cultures were fixed in paraformaldehyde, treated with acetone, anti-tubulin and a second antibody coupled to FITC, fluorescence was associated with cytoskeletal and axonemal microtubules. Cilia covering the apical surface of the ciliated tracheal cells fluoresced very brightly thus facilitating identification of this cell type. Electron microscopy of tracheal cultures fixed as above, treated with Triton-X 100 and incubated in anti-tubulin and protein A coupled to colloidal gold resulted in the highly specific localization of tubulin in ciliary axonemes and basal bodies. Omission of primary or secondary antibody resulted in extremely low levels of fluorescence while no colloidal gold particles could be detected in cultures at the electron microscopy level when rabbit anti-tubulin was omitted.

摘要

用抗微管蛋白抗体和胶体金对纤毛气管上皮细胞培养物进行免疫细胞化学研究。当兔气管培养物用多聚甲醛固定、丙酮处理、加入抗微管蛋白抗体和与异硫氰酸荧光素(FITC)偶联的二抗时,荧光与细胞骨架微管和轴丝微管相关。覆盖纤毛气管细胞顶端表面的纤毛发出非常明亮的荧光,从而便于识别这种细胞类型。对如上固定的气管培养物进行电子显微镜检查,用曲拉通X-100处理,然后在抗微管蛋白抗体和与胶体金偶联的蛋白A中孵育,结果微管蛋白在纤毛轴丝和基体中高度特异性定位。省略一抗或二抗会导致荧光水平极低,而当省略兔抗微管蛋白抗体时,在电子显微镜水平的培养物中检测不到胶体金颗粒。

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