Picosecond Laser Scanning Microscopy
Upgrade Your
Leica TCS SP / SP2 MP for
Lifetime Imaging
Fluorescence
Lifetime Imaging (FLIM) has become a new powerful method to investigate
molecular interactions, metabolic reactions and energy transfer in cells
and subcellular structures. These effects cause changes in the
fluorescence quantum efficiency and thus in the fluorescence lifetime.
Since the fluorescence lifetime does not depend on the unknown dye
concentration it is a direct measure for the quantum efficiency. It
therefore gives a more direct access to the investigated effects than
the fluorescence intensity. Furthermore, the fluorescence lifetime can
be used to separate the fluorescence of different luminophores in the
cells if the components cannot be distinguished by their fluorescence
spectra.
Recording
time-resolved fluorescence images can be achieved by combining the Leica
TCS SP2 Laser Scanning Microscope with Ti:Sa laser excitation and a new
Time-Correlated Single Photon Counting (TCSPC) Imaging technique
introduced by Becker & Hickl.

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