*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy*****
It will matter greatly what you are imaging the light scattering of the
sample. I have added the DeepSee compensator to our Ti:Sa, MP setup for
imaging blood vessels in mice. I experienced significant increase in
brightness (3X) and mirror depth improvement (~10-15%). Hope that this
helps.
Richard Cole
Research Scientist V
Director: Advanced Light Microscopy Core Unit
Wadsworth Center
Research Assistant Professor
Dept. of Biomedical Sciences
School of Public Health State University of New York
P.O. Box 509 Albany N.Y. 12201-0509
518-474-7048 Phone
518-474-4430 Fax
Email <mailto:
[hidden email]>
[hidden email]
Website <
http://www.wadsworth.org/cores/alm/index.htm>
www.wadsworth.org/cores/alm/index.htm
> Hi everybody,
> I am planning to image fluorescent neurons in vivo approximately 200
> um below the pia with a standard Ti:Sa laser.
> I wonder if there is a clear advantage to use pulse compression to
> compensate for dispersion of pulses due to tissue.
> I understand theoretical arguments in favor of pulse compression.
> However from an experimental point of view, are there some people here
> in the list that have experienced some gain (in lowering the intensity
> of the exciting beam for example).
> Any comments would be greatly appreciated.
> Thanks a lot
> Stephane
>
IMPORTANT NOTICE: This e-mail and any attachments may contain
confidential or sensitive information which is, or may be, legally
privileged or otherwise protected by law from further disclosure. It
is intended only for the addressee. If you received this in error or
from someone who was not authorized to send it to you, please do not
distribute, copy or use it or any attachments. Please notify the
sender immediately by reply e-mail and delete this from your
system. Thank you for your cooperation.