Yamashita Shuji
Electron Microscope Laboratory, School of Medicine, Keio University, Tokyo, Japan.
Methods Mol Biol. 2010;657:237-48. doi: 10.1007/978-1-60761-783-9_19.
We describe a standardized method of fixation, antigen retrieval, and image contrasting for post-embedding immunoelectron microscopy. Tissues are fixed with formaldehyde solutions containing Ca(2+) and Mg(2+) ions at pH 7.4 and then at pH 8.5. After dehydration with dimethylformamide, the specimens are embedded in LR-White resin. For antigen retrieval, ultrathin sections are heated in 20 mM Tris-HCl buffer (pH 9.0) for 1 h at 95 degrees C. After immunogold labeling, the sections are treated with a mixture of tannic acid and glutaraldehyde, with OsO(4) solution, and then double-stained with uranyl acetate and lead citrate. The standardized method yields strong and reproducible immunoreactions for many antigens showing excellent image contrast without destruction of fine structures.
我们描述了一种用于包埋后免疫电子显微镜的固定、抗原修复和图像对比的标准化方法。组织先用含有Ca(2+)和Mg(2+)离子、pH值为7.4的甲醛溶液固定,然后用pH值为8.5的甲醛溶液固定。用二甲基甲酰胺脱水后,将标本包埋在LR-White树脂中。为了进行抗原修复,超薄切片在20 mM Tris-HCl缓冲液(pH 9.0)中于95℃加热1小时。免疫金标记后,切片用鞣酸和戊二醛的混合物、OsO(4)溶液处理,然后用醋酸铀和柠檬酸铅进行双重染色。该标准化方法对许多抗原产生强烈且可重复的免疫反应,显示出优异的图像对比度,且不会破坏精细结构。