Himmelhoch S
Department of Biological Services, Weizmann Institute of Science, Rehovot, Israel.
Microsc Res Tech. 1994 Sep 1;29(1):23-8. doi: 10.1002/jemt.1070290104.
Ultra-thin frozen sections are ideal substrates for immunolabelling in high resolution electron microscopy. However, visualization of subcellular structures is inferior to that obtained with corresponding plastic sections. Although negative staining is generally effective and even superior to positive staining, the accumulated stain is often too heavy, obscuring morphology and markers used for immunocytochemical localization of antigens. This paper describes the development of a modified negative contrast staining technique in which a high concentration of uranyl acetate is mixed with methyl cellulose at a low pH. Application of this stain to cryosections of cells and tissue resulted in improved visualization of morphological structures characterized by negative images of membranes and cell organelles. Use of this stain is advantageous for morphological and immunocytochemical studies involving ultra-thin frozen sections.
超薄冰冻切片是高分辨率电子显微镜免疫标记的理想底物。然而,亚细胞结构的可视化效果不如相应塑料切片。尽管负染色通常有效,甚至优于正染色,但累积的染色剂往往过重,会掩盖用于抗原免疫细胞化学定位的形态和标记物。本文描述了一种改良的负性对比染色技术的开发,即在低pH值下将高浓度醋酸铀与甲基纤维素混合。将这种染色剂应用于细胞和组织的冷冻切片,可改善以膜和细胞器负像为特征的形态结构的可视化效果。这种染色剂的使用有利于涉及超薄冰冻切片的形态学和免疫细胞化学研究。