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J Microsc ; 229(Pt 1): 104-14, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18173649

ABSTRACT

A scanning-less single-photon counting system for FLIM and fluorescence anisotropy wide-field imaging is described and characterized in this paper. The two polarizations of the fluorescence are divided by a Glan prism and acquired at the same time by the Q(A) detector. Fluorescence decay profiles can be reconstructed for any desired area up to each pixel and used to calculate time-resolved fluorescence anisotropy decays.


Subject(s)
Fluorescence Polarization , Fluorescence Resonance Energy Transfer/methods , Microscopy, Fluorescence/methods , Rhodamines/chemistry , Coloring Agents , Fluorescence Resonance Energy Transfer/instrumentation , Microscopy, Fluorescence/instrumentation , Photochemistry
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