共焦
显微镜
共焦显微镜
扫描共焦电子显微镜
显微镜
分辨率(逻辑)
材料科学
光学
4Pi显微镜
荧光显微镜
荧光
物理
计算机科学
人工智能
多光子荧光显微镜
作者
Giulia M. R. De Luca,Emilie Desclos,Ronald M. P. Breedijk,Laura Dolz‐Edo,Gertien J. Smits,Leila Nahidiazar,Pascal Bielefeld,L. PICAVET,Carlos P. Fitzsimons,Ron A. Hoebe,Erik M. M. Manders
摘要
Summary The new high‐sensitive and high‐resolution technique, Re‐scan Confocal Microscopy (RCM), is based on a standard confocal microscope extended with a re‐scan detection unit. The re‐scan unit includes a pair of re‐scanning mirrors that project the emission light onto a camera in a scanning manner. The signal‐to‐noise ratio of Re‐scan Confocal Microscopy is improved by a factor of 4 compared to standard confocal microscopy and the lateral resolution of Re‐scan Confocal Microscopy is 170 nm (compared to 240 nm for diffraction limited resolution, 488 nm excitation, 1.49 NA). Apart from improved sensitivity and resolution, the optical setup of Re‐scan Confocal Microscopy is flexible in its configuration in terms of control of the mirrors, lasers and filters. Because of this flexibility, the Re‐scan Confocal Microscopy can be configured to address specific biological applications. In this paper, we explore a number of possible configurations of Re‐scan Confocal Microscopy for specific biomedical applications such as multicolour, FRET, ratio‐metric (e.g. pH and intracellular Ca 2+ measurements) and FRAP imaging.
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