光学切片
共焦
共焦显微镜
显微镜
薄层荧光显微镜
光学显微镜
荧光显微镜
光学
显微镜
扫描共焦电子显微镜
材料科学
超分辨显微术
分辨率(逻辑)
扫描离子电导显微镜
电子显微镜
荧光
计算机科学
人工智能
扫描电子显微镜
物理
作者
José-Angel Conchello,Jeff W. Lichtman
出处
期刊:Nature Methods
[Springer Nature]
日期:2005-11-18
卷期号:2 (12): 920-931
被引量:663
摘要
Confocal scanning microscopy, a form of optical sectioning microscopy, has radically transformed optical imaging in biology. These devices provide a powerful means to eliminate from images the background caused by out-of-focus light and scatter. Confocal techniques can also improve the resolution of a light microscope image beyond what is achievable with widefield fluorescence microscopy. The quality of the images obtained, however, depends on the user's familiarity with the optical and fluorescence concepts that underlie this approach. We describe the core concepts of confocal microscopes and important variables that adversely affect confocal images. We also discuss data-processing methods for confocal microscopy and computational optical sectioning techniques that can perform optical sectioning without a confocal microscope.
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