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Curr Opin Neurobiol. 2004 Oct;14(5):599-609.

Concepts for nanoscale resolution in fluorescence microscopy.

Author information

1
Max Planck Institute for Biophysical Chemistry, Department of NanoBiophotonics, Am Fassberg 11, 37070 Göttingen, Germany. hell@nanoscopy.de

Abstract

Spatio-temporal visualization of cellular structures by fluorescence microscopy has become indispensable in biology. However, the resolution of conventional fluorescence microscopy is limited by diffraction to about 180 nm in the focal plane and to about 500 nm along the optic axis. Recently, concepts have emerged that overcome the diffraction resolution barrier fundamentally. Formed on the basis of reversible saturable optical transitions, these concepts might eventually allow us to investigate hitherto inaccessible details within live cells.

PMID:
15464894
DOI:
10.1016/j.conb.2004.08.015
[Indexed for MEDLINE]

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