| Literature DB >> 18469823 |
Manuel F Juette1, Travis J Gould, Mark D Lessard, Michael J Mlodzianoski, Bhupendra S Nagpure, Brian T Bennett, Samuel T Hess, Joerg Bewersdorf.
Abstract
Imaging volumes as thick as whole cells at three-dimensional (3D) super-resolution is required to reveal unknown features of cellular organization. We report a light microscope that generates images with translationally invariant 30 x 30 x 75 nm resolution over a depth of several micrometers. This method, named biplane (BP) FPALM, combines a double-plane detection scheme with fluorescence photoactivation localization microscopy (FPALM) enabling 3D sub-diffraction resolution without compromising speed or sensitivity.Mesh:
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Year: 2008 PMID: 18469823 DOI: 10.1038/nmeth.1211
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547