Live cell spinning disk microscopy.

Ralph Gräf; Jens Rietdorf; Timo Zimmermann

doi:10.1007/b102210

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Live cell spinning disk microscopy.

Ralph Gräf·Jens Rietdorf·Timo Zimmermann

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Abstract

In vivo microscopy of dynamic processes in cells and organisms requires very fast and sensitive acquisition methods. Confocal laser scanning microscopy is inherently speed-limited by the requirement of beam scanning movements. In contrast to single beam scanning systems, the parallelized approach of multi-beam scanning is much faster. Spinning disk confocal microscopes are therefore very suited for fast in vivo imaging. The principles of spinning disk microscopy will be explained in this chapter and a thorough comparison of the performance of single beam and multi-beam scanning systems is made and illustrated with an example of in vivo imaging in Dictyostelium discoideum.

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Animals Centrosome Dictyostelium Equipment Design Equipment Failure Analysis Image Enhancement Microscopy, Confocal Microscopy, Fluorescence Microscopy, Video Rotation Journal Article Review

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Ralph Gräf, Jens Rietdorf, Timo Zimmermann. 2005. Live cell spinning disk microscopy.. https://doi.org/10.1007/b102210

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