Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
I am interested in hearing from researchers who do live cell imaging on upright
scopes. Is it being done with dipping objectives in regular medium, or with
special chambers and flow cells? If dipping objectives are used, does this work
for long experiments (days), or does the culture get contaminated right away?
You experiences and collective wisdom will be greatly appreciated.
--aryeh
--
Aryeh Weiss
School of Engineering
Bar Ilan University
Ramat Gan 52900 Israel
Ph: 972-3-5317638
FAX: 972-3-7384050