Fluorescence lifetime measurements in confocal microscopy of neurons labeled with multiple fluorophores

Author:

Brismar Hjalmar,UIfhake Brun

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Reference31 articles.

1. Weesendorf, M.W. 1990. Characterization and use of multi-color fluorescence microscopic technique, in Analysis of neuronal microcircuits and synaptic interaction. Bjrklund, A., Hkfelt, T., Wouterlood, F.Q., and van den Pol, A.N. (eds). Elsevier Publishing, Amsterdam.

2. Wessendorf, M.W. and Brelje, T.C. 1993. Multicolor fluorescence microscopy using the laser-scanning confocal microscope. Neuro. Protocols 2: 121.

3. Mossberg, K., Arvidsson, U., and Ulfhake, B. 1990. Computerized quantification of immunofluorescence-labeled axon terminals and analysis of co-localization of neurochemicals in axon terminals with confocal scanning laser microscope. J. Histochem. Cytochem. 38: 179.

4. Lakowicz, J.R. 1983. Principles of fluorescence spectroscopy. Plenum Press, New York.

5. Åslund, N. and Carlsson, K. 1994. Simultaneous life-time imaging of two fluorophores using a confocal laser microscope. IS&T/SPIE International Symposium on Electronic Imaging, Three–dimensional Microscopy: Image Acquisition and Processing. SPIE 2184, Proceedings.

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