Namork E, Heier H E
Department of Methodology, National Institute of Public Health, Oslo, Norway.
J Electron Microsc Tech. 1989 Feb;11(2):102-8. doi: 10.1002/jemt.1060110203.
Silver enhancement of immunogold-labeled cells was carried out to increase the applicability of colloidal gold probes for visualization in the backscatter electron imaging (BEI) mode of a scanning electron microscope. Optimum conditions were established for single particle discrimination and differential counting of labeling density at low magnifications. Red blood cells double-labeled with 15 + 40 nm and 5 + 20 nm gold probes were silver-enhanced for 6 min and 20 min, respectively, at which times both pairs of labels increased to about 25 + 50 nm. The gold probes still appeared spherical after enhancement and were easily discriminated. Cells were also single-labeled with the above probes and enhanced accordingly. The present method enables visualization of individual particles of any probe size, labeling one, or simultaneously two, antigenic sites on cell surfaces. The silver enhancement procedure thereby allows cells to be labeled with small probes with increased labeling efficiency.
对免疫金标记细胞进行银增强,以提高胶体金探针在扫描电子显微镜背散射电子成像(BEI)模式下用于可视化的适用性。确定了在低放大倍数下进行单颗粒辨别和标记密度差异计数的最佳条件。用15 + 40 nm和5 + 20 nm金探针双标记的红细胞分别进行6分钟和20分钟的银增强,此时两对标记物均增加到约25 + 50 nm。增强后金探针仍呈球形,易于辨别。细胞也用上述探针进行单标记并相应增强。本方法能够可视化任何探针大小的单个颗粒,标记细胞表面的一个或同时两个抗原位点。银增强程序从而允许用小探针标记细胞,提高标记效率。