显微镜
薄层荧光显微镜
荧光显微镜
显微镜
全内反射荧光显微镜
共焦显微镜
超分辨显微术
扫描共焦电子显微镜
光学显微镜
分辨率(逻辑)
光激活定位显微镜
光学
双光子激发显微术
光学切片
激光显微镜
材料科学
共焦
荧光
计算机科学
物理
扫描电子显微镜
人工智能
作者
Michael J. Sanderson,Ian F. Smith,Ian Parker,Martin D. Bootman
出处
期刊:CSH Protocols
[Cold Spring Harbor Laboratory]
日期:2014-10-01
卷期号:2014 (10): pdb.top071795-pdb.top071795
被引量:301
标识
DOI:10.1101/pdb.top071795
摘要
Fluorescence microscopy is a major tool with which to monitor cell physiology. Although the concepts of fluorescence and its optical separation using filters remain similar, microscope design varies with the aim of increasing image contrast and spatial resolution. The basics of wide-field microscopy are outlined to emphasize the selection, advantages, and correct use of laser scanning confocal microscopy, two-photon microscopy, scanning disk confocal microscopy, total internal reflection, and super-resolution microscopy. In addition, the principles of how these microscopes form images are reviewed to appreciate their capabilities, limitations, and constraints for operation.
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