Wergin W P, Yaklich R W, Roy S, Joy D C, Erbe E F, Murphy C A, Pooley C D
Nematology Laboratory, USDA-ARS, Beltsville, MD 20705, USA.
Scanning. 1997 Sep;19(6):386-95.
A field-emission scanning electron microscope (FESEM) equipped with the standard secondary electron (SE) detector was used to image thin (70-90 nm) and thick (1-3 microns) sections of biological materials that were chemically fixed, dehydrated, and embedded in resin. The preparation procedures, as well as subsequent staining of the sections, were identical to those commonly used to prepare thin sections of biological material for observation with the transmission electron microscope (TEM). The results suggested that the heavy metals, namely, osmium, uranium, and lead, that were used for postfixation and staining of the tissue provided an adequate SE signal that enabled imaging of the cells and organelles present in the sections. The FESEM was also used to image sections of tissues that were selectively stained using cytochemical and immunocytochemical techniques. Furthermore, thick sections could also be imaged in the SE mode. Stereo pairs of thick sections were easily recorded and provided images that approached those normally associated with high-voltage TEM.
使用配备标准二次电子(SE)探测器的场发射扫描电子显微镜(FESEM)对经过化学固定、脱水并包埋在树脂中的生物材料薄切片(70 - 90纳米)和厚切片(1 - 3微米)进行成像。制备程序以及切片的后续染色与通常用于制备生物材料薄切片以供透射电子显微镜(TEM)观察的程序相同。结果表明,用于组织后固定和染色的重金属,即锇、铀和铅,提供了足够的二次电子信号,使得能够对切片中存在的细胞和细胞器进行成像。FESEM还用于对使用细胞化学和免疫细胞化学技术进行选择性染色的组织切片进行成像。此外,厚切片也可以在二次电子模式下成像。厚切片的立体图像对很容易记录,并且提供的图像接近通常与高压TEM相关的图像。