Tang G, Tang X, Gan D
Electron Microscopy Laboratory, West China University of Medical Sciences, Chengdu 610041.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 1999 Jun;16(2):237-9.
A method of preparing the section of eye tissue for transmission electron microscopy (TEM) is recommended. The tissue was prefixed with a mixed solution of 4% paraformaldehyde and 2.5% glutaraldehyde and followed by softening in 3% EDTA solution for 20 minutes, then the tissue was fixed in 1% osmium tetroxide, dehydrated in series acetone, infiltrated in Epox 812 for a longer, and embeded. Ultrathin sections were cut with glass knives or diamond knife, stained with uranyl acetate and lead citrate and examined with H600-IV. The advantage of this method is that the ultrastructures of tissues are well preserved without any damage and distortion. The main points of the procedure of preparation have been discussed.
推荐一种用于透射电子显微镜(TEM)的眼组织切片制备方法。组织先用4%多聚甲醛和2.5%戊二醛的混合溶液预固定,然后在3%乙二胺四乙酸(EDTA)溶液中软化20分钟,接着将组织用1%四氧化锇固定,依次在丙酮中脱水,在Epox 812中较长时间渗透并包埋。用玻璃刀或钻石刀切割超薄切片,用醋酸铀和柠檬酸铅染色,并用H600-IV进行观察。该方法的优点是组织的超微结构得到良好保存,无任何损伤和变形。已讨论了制备过程的要点。