Paper
30 March 2005 Fluorescence lifetime images and correlation spectra obtained by multidimensional TCSPC
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Abstract
Multi-dimensional time-correlated single photon counting (TCSPC) is based on the excitation of the sample by a high-repetition rate laser and the detection of single photons of the fluorescence signal in several detection channels. Each photon is characterised by its time in the laser period, its detection channel number, and several additional variables such as the coordinates of an image area, or the time from the start of the experiment. Combined with a confocal or two-photon laser scanning microscope and a pulsed laser, multi-dimensional TCSPC makes a fluorescence lifetime technique with multi-wavelength capability, near-ideal counting efficiency, and the capability to resolve multi-exponential decay functions. We show that the same technique and the same hardware can be used to for precision fluorescence decay analysis, fluorescence correlation spectroscopy (FCS), and fluorescence intensity distribution analysis (FIDA and FILDA) in selected spots of a sample.
© (2005) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Wolfgang Becker, Axel Bergmann, Elke Haustein, Zdenek Petrasek, Petra Schwille, Christoph U. Biskup, Tiemo Anhut, Iris Riemann, and Karsten Konig "Fluorescence lifetime images and correlation spectra obtained by multidimensional TCSPC", Proc. SPIE 5700, Multiphoton Microscopy in the Biomedical Sciences V, (30 March 2005); https://doi.org/10.1117/12.588990
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Cited by 17 scholarly publications.
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KEYWORDS
Luminescence

Fluorescence correlation spectroscopy

Fluorescence lifetime imaging

Sensors

Fluorescence resonance energy transfer

Microscopes

Proteins

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