| Literature DB >> 19536533 |
Liisa M Hirvonen1, Kai Wicker, Ondrej Mandula, Rainer Heintzmann.
Abstract
Due to diffraction, the resolution of imaging emitted light in a fluorescence microscope is limited to about 200 nm in the lateral direction. Resolution improvement by a factor of two can be achieved using structured illumination, where a fine grating is projected onto the sample, and the final image is reconstructed from a set of images taken at different grating positions. Here we demonstrate that with the help of a spatial light modulator, this technique can be used for imaging slowly moving structures in living cells.Mesh:
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Year: 2009 PMID: 19536533 DOI: 10.1007/s00249-009-0501-6
Source DB: PubMed Journal: Eur Biophys J ISSN: 0175-7571 Impact factor: 1.733