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Hi,
Does anybody know how the laser intensity is monitored in a commercial
confocal system? How the laser fluctuation (they are very small,+/-3%) affects
the fluorescence image collection? How it is corrected if it exists?
Thank you!
Sincerely,
Peng Xi
Purdue University Cytometry Laboratories
Bindley Bioscience Center
1203 W. State Street
West Lafayette, IN 47907
Tel: 765-494-0757
Fax: 765-494-0517
http://web.ics.purdue.edu/~pxi