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.
Original language | English |
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Pages (from-to) | 807-812 |
Number of pages | 6 |
Journal | European Biophysics Journal |
Volume | 38 |
Issue number | 6 |
DOIs | |
Publication status | Published - 1 Jul 2009 |
Externally published | Yes |