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High-resolution imaging by scanning electron microscopy of semithin sections in correlation with light microscopy.

机译:通过扫描电子显微镜对半薄切片进行高分辨率成像,并与光学显微镜相关联。

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摘要

In this study, we introduce scanning electron microscopy (SEM) of semithin resin sections. In this technique, semithin sections were adhered on glass slides, stained with both uranyl acetate and lead citrate, and observed with a backscattered electron detector at a low accelerating voltage. As the specimens are stained in the same manner as conventional transmission electron microscopy (TEM), the contrast of SEM images of semithin sections was similar to TEM images of ultrathin sections. Using this technique, wide areas of semithin sections were also observed by SEM, without the obstruction of grids, which was inevitable for traditional TEM. This study also applied semithin section SEM to correlative light and electron microscopy. Correlative immunofluorescence microscopy and immune-SEM were performed in semithin sections of LR white resin-embedded specimens using a FluoroNanogold-labeled secondary antibody. Because LR white resin is hydrophilic and electron stable, this resin is suitable for immunostaining and SEM observation. Using correlative microscopy, the precise localization of the primary antibody was demonstrated by fluorescence microscopy and SEM. This method has great potential for studies examining the precise localization of molecules, including Golgi- and ER-associated proteins, in correlation with LM and SEM.
机译:在这项研究中,我们介绍了半薄树脂切片的扫描电子显微镜(SEM)。在这种技术中,将半薄切片粘附在载玻片上,用乙酸铀酰和柠檬酸铅染色,并在低加速电压下用反向散射电子检测器观察。由于样品以与常规透射电子显微镜(TEM)相同的方式染色,因此半薄切片的SEM图像的对比度类似于超薄切片的TEM图像。使用这项技术,还可以通过SEM观察到大面积的半薄截面,而不会阻塞网格,这是传统TEM不可避免的。这项研究还将半薄截面SEM应用于相关的光学和电子显微镜。使用荧光纳米金标记的第二抗体在LR白色树脂包埋的标本的半薄切片中进行相关的免疫荧光显微镜检查和免疫SEM。由于LR白色树脂具有亲水性和电子稳定性,因此适合用于免疫染色和SEM观察。使用相关显微镜,通过荧光显微镜和SEM证实了第一抗体的精确定位。这种方法对于研究与LM和SEM相关的分子(包括高尔基体和ER相关蛋白)的精确定位具有巨大的潜力。

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