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Proceedings Paper

Fluorescence lifetime imaging microscopy using a tunable continuum source and a Nipkow disk confocal microscope
Author(s): D. Grant; E. Auksorius; D. Schimpf; D. S. Elson; C. Dunsby; J. Requejo-Isidro; I. Munro; M. A. A. Neil; P. M. W. French; P. Courtney
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Paper Abstract

Multi-beam confocal sectioned fluorescence lifetime imaging microscopy is demonstrated using a Yokogawa spinning disk. The single-photon excitation source is a supercontinuum generated from a Ti:sapphire seeded photonic crystalline fibre.

Paper Details

Date Published: 7 October 2005
PDF: 7 pages
Proc. SPIE 5860, Confocal, Multiphoton, and Nonlinear Microscopic Imaging II, 58600K (7 October 2005); doi: 10.1117/12.632952
Show Author Affiliations
D. Grant, Imperial College London (United Kingdom)
E. Auksorius, Imperial College London (United Kingdom)
D. Schimpf, Imperial College London (United Kingdom)
D. S. Elson, Imperial College London (United Kingdom)
C. Dunsby, Imperial College London (United Kingdom)
J. Requejo-Isidro, Imperial College London (United Kingdom)
I. Munro, Imperial College London (United Kingdom)
M. A. A. Neil, Imperial College London (United Kingdom)
P. M. W. French, Imperial College London (United Kingdom)
P. Courtney, Perkin Elmer Inc. (United Kingdom)


Published in SPIE Proceedings Vol. 5860:
Confocal, Multiphoton, and Nonlinear Microscopic Imaging II
Tony Wilson, Editor(s)

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