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A protocol for single-source dual-pulse stimulated emission depletion setup with Bessel modulation
Microscopy Research and Technique ( IF 2.5 ) Pub Date : 2021-09-06 , DOI: 10.1002/jemt.23922
Xinzhu Xu 1, 2 , Kun Zhao 1, 2 , Wei Ren 1 , Zhaoyang Wu 1 , Wentao Yu 3 , Chendi Shao 3 , Kebin Shi 3, 4 , Peng Xi 1, 5, 6
Affiliation  

STimulated Emission Depletion (STED) microscopy attains super-resolution in biological imaging beyond the diffraction limit. Here, we give a concise protocol to construct a dual-pulse STED setup with one super-continuum laser. Moreover, a flexible and dismountable Bessel modulation module is introduced for potential 2D-stack STED imaging. Experiments and notices are introduced in detail, with discussion on some important check-points for STED, such as detector saturation. Finally, the results validate the system working.

中文翻译:

具有贝塞尔调制的单源双脉冲受激发射耗尽设置协议

受激发射损耗 (STED) 显微镜在超出衍射极限的生物成像中获得超分辨率。在这里,我们给出了一个简洁的协议,用一个超连续激光器构建双脉冲 STED 设置。此外,为潜在的二维堆叠 STED 成像引入了灵活且可拆卸的贝塞尔调制模块。详细介绍了实验和注意事项,并讨论了STED的一些重要检查点,例如探测器饱和度。最后,结果验证了系统的工作。
更新日期:2021-09-06
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