| Literature DB >> 19118681 |
Travis J Gould1, Samuel T Hess.
Abstract
Biological imaging has been limited by the finite resolution of light microscopy. Recent developments in ultra-high-resolution microscopy methods, many of which are based on fluorescence, are breaking the diffraction barrier; it is becoming possible to image intracellular protein distributions with resolution of tens of nanometers or better. Fluorescence photoactivation localization microscopy (FPALM) is an example of such an ultra-high-resolution method which can image living or fixed cells with demonstrated lateral resolution of better than 20 nm. A detailed description of the methods involved in FPALM imaging of biological samples is presented here, accompanied by comparison with existing methods from the literature.Mesh:
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Year: 2008 PMID: 19118681 DOI: 10.1016/S0091-679X(08)00612-2
Source DB: PubMed Journal: Methods Cell Biol ISSN: 0091-679X Impact factor: 1.441