For further information, please contact:
Subject to change.
Carl Zeiss
Advanced Imaging Microscopy
07740 Jena, Germany
Phone: +49 36 41-64 34 00
Fax:
+49 36 41-64 31 44
E-Mail: micro@zeiss.de
www.zeiss.de/lsm
45-0039 e/04.05
Printed on envir
onment-friendly paper
,
bleached without the use of chlorine.
REFERENCES
Amiri H., Schulz G., Schaefer M. (2003)
FRET-based analysis of TRPC subunit stoichiometry.
Cell calcium, 33(5-6):463-70.
Carl Zeiss (2000)
Confocal Laser Scanning Microscopy –
Principles. 45-0029 e/09.03
Carl Zeiss (2002)
Colocalization – Analysis and Visualization.
45-0012 e/11.02
Carl Zeiss (2002)
Spectral Separation of Multifluorescence Labels
with the LSM 510 META.
40-546 e/05.02
Diaspro A. (2001)
Confocal and Two-Photon Microscopy :
Foundations, Applications and Advances,
Wiley-Liss, New York
Dickinson M.E. (2001)
Multi-spectral imaging and Linear unmixing
add a whole new dimension to laser scanning
fluorescence microscopy.
Bio Techniques 31/6, 1272-1278.
Gordon G,W. (1998)
Quantitative Fluorescence Resonance
Energy Transfer Measurements Using
Fluorescence Microscopy.
Biophys J, May 1998, p. 2702-2713, Vol. 74, No. 5
Pawley J.B. (1995)
Handbook of Biological Confocal Microscopy.
Plenum Press, New York
Selvin P.R. (2000)
The renaissance of fluorescence resonance energy
transfer. Nat Struct Biol. 7(9):730-4. Review.
LINKS
Carl Zeiss website on
contrasting techniques in light microscopy
www.zeiss.de/contrasts
EAMNET website on FRAP
www.embl-heidelberg.de/eamnet/html/
teaching_modules.html