Mutasa H C
Department of Medical Laboratory Technology, University of Zimbabwe Medical School, Harare.
Biotech Histochem. 1995 Jul;70(4):194-201. doi: 10.3109/10520299509107312.
A diaminobenzidine posttreatment employing osmium tetroxide and potassium ferrocyanide was successfully used to intensify the diaminobenzidine stain formed by photoconversion of immunofluorescent labelling. Lactoferrin labelled granules became visible following the photoconversion process. Adequate diaminobenzidine staining was obtained after irradiating the cytospin preparations with ultraviolet light for 30-40 min. The diaminobenzidine stain had advantages over the fluorescent stain owing to its greater stability, greater density, and ability to be intensified. The enhancement procedure intensified both the color and density of the diaminobenzidine product. Consequently, shorter irradiation times could be used. Osmium tetroxide solutions of 3-4% increased the intensity with minimal background staining. Ultrastructural immunogold cytochemistry on ultrathin sections confirmed the existence of the lactoferrin labelled structures observed by light microscopy of cytospin preparations indicating that these were secondary granules. The photomicroscopy procedures used in this study were simple to perform and could be applied to studies of other cellular antigens prior to using immunoultramicroscopy.
采用四氧化锇和亚铁氰化钾进行二氨基联苯胺后处理,成功用于增强免疫荧光标记光转换形成的二氨基联苯胺染色。光转换过程后,乳铁蛋白标记的颗粒变得可见。用紫外光照射细胞涂片制剂30 - 40分钟后,获得了足够的二氨基联苯胺染色。二氨基联苯胺染色因其更高的稳定性、更高的密度以及可增强的能力,比荧光染色具有优势。增强程序增强了二氨基联苯胺产物的颜色和密度。因此,可以使用更短的照射时间。3 - 4%的四氧化锇溶液增加了强度,背景染色最小。超薄切片的超微结构免疫金细胞化学证实了细胞涂片制剂光镜观察到的乳铁蛋白标记结构的存在,表明这些是次级颗粒。本研究中使用的显微摄影程序操作简单,可在使用免疫超微镜之前应用于其他细胞抗原的研究。