Silver enhancement of gold probes (5-40 nm): single and double labeling of antigenic sites on cell surfaces imaged with backscattered electrons.

E Namork, H E Heier
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引用次数: 31

Abstract

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.

金探针的银增强(5-40 nm):用背散射电子成像细胞表面抗原位点的单和双标记。
对免疫金标记的细胞进行银增强,以提高胶体金探针在扫描电镜背散射电子成像(BEI)模式下的可视化适用性。确定了低倍率下单粒子识别和标记密度微分计数的最佳条件。用15 + 40 nm和5 + 20 nm金探针双标记的红细胞分别银增强6 min和20 min,此时两对标记都增加到25 + 50 nm左右。金探针经增强后仍呈球形,易被识别。细胞也用上述探针单标记并相应增强。本方法能够可视化任何探针大小的单个颗粒,标记细胞表面上的一个或同时两个抗原位点。因此,银增强程序允许用小探针标记细胞,从而提高标记效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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