扫描电镜
显微镜
光学
薄层荧光显微镜
全内反射
全内反射荧光显微镜
超分辨显微术
材料科学
荧光团
显微镜
光学显微镜
荧光显微镜
光学切片
分辨率(逻辑)
受激发射
扫描共焦电子显微镜
荧光
扫描电子显微镜
激光器
物理
人工智能
计算机科学
作者
Travis J. Gould,Jordan Myers,Joerg Bewersdorf
出处
期刊:Optics Express
[The Optical Society]
日期:2011-06-27
卷期号:19 (14): 13351-13351
被引量:50
摘要
Stimulated emission depletion (STED) microscopy achieves diffraction-unlimited resolution in far-field fluorescence microscopy well below 100 nm. As common for (single-lens) far-field microscopy techniques, the lateral resolution is better than the axial sectioning capabilities. Here we present the first implementation of total internal reflection (TIR) illumination into STED microscopy which limits fluorophore excitation to ~70 nm in the vicinity of the cover slip while simultaneously providing ~50 nm lateral resolution. We demonstrate the performance of this new microscope technique with fluorescent bead test samples as well as immuno-stained microtubules. Total internal reflection STED microscopy provides superior axial sectioning capabilities with the potential to reduce photo-bleaching and photo-damage in live cell imaging.
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