Opas M, Kalnins V I
Eur J Cell Biol. 1984 Jan;33(1):60-5.
To study the relationship between microfilament distribution and adhesion patterns in the same cultured cell, we have employed a simple glutaraldehyde-formaldehyde fixation technique followed by permeabilization of the cells in buffered Triton X-100. This method gives an excellent preservation of cellular morphology in general and of adhesion patterns in particular for examination with surface reflection interference microscopy. It also permits the concomitant use of the actin-specific fluorescent probe NBD-phallacidin to visualize the distribution of microfilaments.
为了研究同一培养细胞中微丝分布与黏附模式之间的关系,我们采用了一种简单的戊二醛 - 甲醛固定技术,随后用缓冲的Triton X - 100使细胞通透。总体而言,这种方法能出色地保存细胞形态,尤其适合用于表面反射干涉显微镜检查黏附模式。它还允许同时使用肌动蛋白特异性荧光探针NBD - 鬼笔环肽来可视化微丝的分布。