All these formulas for confocal microscope resolution assume a
homogeneously illuminated back-aperture, which is not always the case in
commercially available microscopes due to the Gaussian intensity profile
of the excitation laser beam. Therefore, the lateral resolution of a
confocal microscope can even be worse than of a widefield fluorescence
microscope with arc-lamp illumination.
--
arwed weigel
abteilung fuer neurophysiology und zellulaere biophysik
universitaet goettingen
humboldtallee 23
37073 goettingen
phon +49 (0)551 3912201
fax +49 (0)551 398399