Resolution doubling in fluorescence microscopy with confocal spinning-disk image scanning microscopy-Reference-Cited by-同舟云学术

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Resolution doubling in fluorescence microscopy with confocal spinning-disk image scanning microscopy

Published:2013-12-09 Issue:52 Volume:110 Page:21000-21005
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Schulz O.,Pieper C.,Clever M.,Pfaff J.,Ruhlandt A.,Kehlenbach R. H.,Wouters F. S.,Grosshans J.,Bunt G.,Enderlein J.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference29 articles.

1. Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy

2. Imaging Intracellular Fluorescent Proteins at Nanometer Resolution

3. Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM)

4. Image Scanning Microscopy

5. Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy. SHORT COMMUNICATION

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