期刊
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS
卷 38, 期 6, 页码 807-812出版社
SPRINGER
DOI: 10.1007/s00249-009-0501-6
关键词
Structured illumination microscopy; Live-cell imaging; Resolution improvement
类别
资金
- Medical Research Council
- Carl Zeiss MicroImaging GmbH
- International Agency for Atomic Energy
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.
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