Takizawa Toshihiro, Robinson John M
Department of Physiology and Cell Biology, Ohio State University, Columbus, Ohio 43210, USA.
J Histochem Cytochem. 2003 Jun;51(6):707-14. doi: 10.1177/002215540305100602.
Here we show that ultrathin cryosections of placental tissue can be used as a substrate in immunofluorescence experiments. A high degree of spatial resolution can be achieved in these preparations because there is essentially no out-of-focus fluorescence. Therefore, immunofluorescence microscopy using ultrathin cryosections provides a very useful method for determining the precise subcellular localization of antigens in tissues. In addition, ultrathin cryosections of placenta also serve as a substrate for correlative immunofluorescence and immunoelectron microscopy using FluoroNanogold as the detection system. In correlative microscopy, the exact same structures in the same ultrathin section were observed by both fluorescence and electron microscopy. Using a particle counting procedure and electron microscopy, we compared the labeling obtained with colloidal gold and FluoroNanogold and found a higher number of particles with silver-enhanced FluoroNanogold than with colloidal gold.
在此我们表明,胎盘组织的超薄冷冻切片可作为免疫荧光实验的底物。在这些制备物中可实现高度的空间分辨率,因为基本上不存在离焦荧光。因此,使用超薄冷冻切片的免疫荧光显微镜检查为确定组织中抗原的确切亚细胞定位提供了一种非常有用的方法。此外,胎盘的超薄冷冻切片还可作为使用荧光纳米金作为检测系统的相关免疫荧光和免疫电子显微镜检查的底物。在相关显微镜检查中,通过荧光显微镜和电子显微镜观察同一超薄切片中完全相同的结构。使用颗粒计数程序和电子显微镜,我们比较了用胶体金和荧光纳米金获得的标记,发现银增强的荧光纳米金比胶体金有更多的颗粒。