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High resolution whole-field three-dimensional fluorescence lifetime imaging
Reference
E11178
Principal Investigator / Supervisor
Professor Tony Wilson
Co-Investigators /
Co-Supervisors
Professor Paul Michael William French
,
Professor M. John Lever
Institution
University of Oxford
Department
Engineering Science
Funding type
Research
Value (£)
137,653
Status
Completed
Type
Research Grant
Start date
01/12/1999
End date
30/06/2002
Duration
30 months
Abstract
The aim of this project is to investigate the use of structured excitation in fluorescence microscopy, pioneered at Oxford University, to provide whole-field 3-D sectioning with comparable resolution to confocal microscopy, combined with fluorescence lifetime imaging to map the local chemical and physical fluorophore environment. This novel imaging modality will be implemented using state-of-the-art diode-pumped ultrafast laser technology pioneered at Imperial College. Single and multi-photon excitation of fluorophores with ultrashort pulses in the visible and near infrared spectral region will be applied to standard phantoms and biological tissue in vitro. (Joint with grant E11253).
Summary
unavailable
Committee
Closed Committee - Engineering & Biological Systems (EBS)
Research Topics
X – not assigned to a current Research Topic
Research Priority
X – Research Priority information not available
Research Initiative
BioImaging (BI) [1998]
Funding Scheme
X – not Funded via a specific Funding Scheme
Associated awards:
E11253 High resolution whole-field three dimensional fluorescence lifetime imaging
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