*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
Post images on http://www.imgur.com and include the link in your posting.
*****
Dear Listers,
Thanks a lot for all the input - I have now quite some food for thoughts!
I was not aware of the polarization issues, but will keep this in mind (though the impact
on the final image seems to be dependant on the structure observed).
At least now I have a couple of arguments/points to discuss with Leica and decide what is
doable with our setups.
Cheers
Debbi
PS: obviously, any additional comments will still be read with high interest!
Debora Keller, PhD
FILM - Facility for Imaging by Light Microscopy
- Super-Resolution Microscopy Specialist -
Sir Alexander Fleming Building, desk 408
Imperial College London / South Kensington
Exhibition Road
London SW7 2AZ, UK
Phone: +44 (0)207 594 9793
Mobile: + 44(0) 7760 256 889
E-mail: [log in to unmask]
Website: http://imperial.ac.uk/imagingfacility