Journal
NATURE METHODS
Volume 8, Issue 12, Pages 1044-+Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/NMETH.1734
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Three-dimensional (3D) structured-illumination microscopy (SIM) can double the lateral and axial resolution of a wide-field fluorescence microscope but has been too slow for live imaging. Here we apply 3D SIM to living samples and record whole cells at up to 5 s per volume for >50 time points with 120-nm lateral and 360-nm axial resolution. We demonstrate the technique by imaging microtubules in S2 cells and mitochondria in HeLa cells.
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