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PMID: 15464894 Published · ppublish English Journal Article Review

Concepts for nanoscale resolution in fluorescence microscopy.

Current opinion in neurobiology ·Vol. 14 ·No. 5 ·2004-10-00 ·Pages 599-609

Hell SW, Dyba M, Jakobs S

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.

MeSH Terms
Animals Fluorescence Fluorescent Dyes/standards Humans Image Processing, Computer-Assisted/methods,trends Lenses/standards,trends Microscopy, Fluorescence/methods,trends Optics and Photonics/instrumentation Photic Stimulation/methods
Chemicals
Fluorescent Dyes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hell Stefan W
Max Planck Institute for Biophysical Chemistry, Department of NanoBiophotonics, Am Fassberg 11, 37070 Göttingen, Germany. hell@nanoscopy.de
Dyba Marcus
Jakobs Stefan
Article Info
Journal
Current opinion in neurobiology
Abbr.
Curr Opin Neurobiol
ISSN
0959-4388
Published
2004-10-00
Pages
599-609
Language
English
Region
England
NLM ID
9111376
Subset
IM
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