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Configurations of the Re‐scan Confocal Microscope (RCM) for biomedical applications
Authors:G.M.R. DE LUCA  E. DESCLOS  R.M.P. BREEDIJK  L. DOLZ‐EDO  G.J. SMITS  L. NAHIDIAZAR  P. BIELEFELD  L. PICAVET  C.P. FITZSIMONS  R. HOEBE  E.M.M. MANDERS
Affiliation:1. Van Leeuwenhoek Centre for Advanced Microscopy, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands;2. Molecular Biology and Microbial Food Safety, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands;3. Division of Cell Biology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam 1066 CX, The Netherlands;4. Center for Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam, The Netherlands;5. Van Leeuwenhoek Centre for Advanced Microscopy, Department of Cell Biology and Histology, Academic Medical Centre, Amsterdam, The Netherlands;6. Nikon Centre of Excellence on Super Resolution Microscopy Development, University of Amsterdam, Amsterdam, The Netherlands
Abstract: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 Ca2+ measurements) and FRAP imaging.
Keywords:High‐sensitive microscopy  live cell imaging  multicolour microscopy  super‐resolution microscopy
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