| Literature DB >> 17339847 |
Peter J Verveer1, Jim Swoger, Francesco Pampaloni, Klaus Greger, Marco Marcello, Ernst H K Stelzer.
Abstract
We report that single (or selective) plane illumination microscopy (SPIM), combined with a new deconvolution algorithm, provides a three-dimensional spatial resolution exceeding that of confocal fluorescence microscopy in large samples. We demonstrate this by imaging large living multicellular specimens obtained in a three-dimensional cell culture. The ability to rapidly image large samples at high resolution with minimal photodamage provides new opportunities especially for the study of subcellular processes in large living specimens.Mesh:
Year: 2007 PMID: 17339847 DOI: 10.1038/nmeth1017
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547