CONFOCALMICROSCOPY Archives

October 2009

CONFOCALMICROSCOPY@LISTS.UMN.EDU

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From:
Martin Wessendorf <[log in to unmask]>
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Date:
Sat, 24 Oct 2009 20:59:31 -0500
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Dear List--

For those of you who have successful multi-photon live-cell imaging 
cores: how have you set up your facilities?  If different users have 
different requirements (e.g. upright vs. inverted stand; temperature/CO2 
control; ability to record electrophysiologically; video-rate scanning 
vs. slower scanning), how do you accommodate them all?  Are there some 
instruments or configurations that are significantly more flexible 
and/or that provide more capabilities for the money spent?  Are there 
some types of experiments that so problematic that they're not worth 
attempting to support?

Thanks.  Responses on- or off-list are welcome.

Martin Wessendorf
-- 
Martin Wessendorf, PhD 	   (612) 626 0145 (office)
Associate Professor	      (612) 624 2991 (lab)	
Dept Neuroscience 	      (612) 624 8118 (FAX)
Univ Minnesota	        e-mail: martinw(at)umn.edu

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