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 |
|---|---|
| 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