Abstract
Background: Fluorescence-based biological imaging has been revolutionized by the recent introduction of superresolution microscopy methods. 3D superresolution microscopy, however, remains a challenge as its implementation by existing superresolution methods is non-trivial. Methods: Here we demonstrate a facile and straightforward 3D superresolution imaging and sectioning of the cytoskeletal network of a fixed cell using superresolution optical fluctuation imaging (SOFI) performed on a conventional lamp-based widefield microscope. Results and Conclusion: SOFI's inherent sectioning capability effectively transforms a conventional widefield microscope into a superresolution 'confocal widefield' microscope.
Original language | English |
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Article number | 2 |
Pages (from-to) | 1-5 |
Number of pages | 5 |
Journal | Optical Nanoscopy |
Volume | 1 |
Issue number | 1 |
DOIs | |
State | Published - 1 Dec 2012 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Atomic and Molecular Physics, and Optics