| Literature DB >> 21765409 |
Thai V Truong1, Willy Supatto, David S Koos, John M Choi, Scott E Fraser.
Abstract
We implemented two-photon scanned light-sheet microscopy, combining nonlinear excitation with orthogonal illumination of light-sheet microscopy, and showed its excellent performance for in vivo, cellular-resolution, three-dimensional imaging of large biological samples. Live imaging of fruit fly and zebrafish embryos confirmed that the technique can be used to image up to twice deeper than with one-photon light-sheet microscopy and more than ten times faster than with point-scanning two-photon microscopy without compromising normal biology.Entities:
Mesh:
Year: 2011 PMID: 21765409 DOI: 10.1038/nmeth.1652
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547