Horisberger M, Rosset J
J Histochem Cytochem. 1977 Apr;25(4):295-305. doi: 10.1177/25.4.323352.
Electron dense markers of a size suitable for transmission electron microscopy and scanning electron microscopy have been prepared with gold granules labeled with a monolayer of specific macromolecules. The optimum conditions for preparing the markers have been ascertained. The method is simple, rapid and seems to be general since gold granules have been labeled with polysaccharides and proteins. As homogeneous populations of gold granules having different sizes can be prepared, the method is also suitable for double marking experiments. The gold technique is illustrated by the localization of polysaccharides and glycoproteins on yeast cell walls and erythrocyte membranes by transmission electron microscopy and on yeast cells and intact erythrocytes by scanning electron microscopy. Good spatial resolution of the marker was achieved in all cases. The method is also suitable for marking thin sections. Spectrophotometric measurements were used to determine the number of gold granules adsorbed per cell.
已制备出大小适合透射电子显微镜和扫描电子显微镜观察的电子致密标记物,其为带有单层特定大分子标记的金颗粒。已确定制备这些标记物的最佳条件。该方法简单、快速,而且似乎具有通用性,因为金颗粒已用多糖和蛋白质进行了标记。由于可以制备出具有不同大小的均匀金颗粒群体,该方法也适用于双重标记实验。通过透射电子显微镜在酵母细胞壁和红细胞膜上以及通过扫描电子显微镜在酵母细胞和完整红细胞上对多糖和糖蛋白进行定位,展示了金标记技术。在所有情况下,标记物都实现了良好的空间分辨率。该方法也适用于标记薄切片。使用分光光度测量法来确定每个细胞吸附的金颗粒数量。