Hello;
I have a colleague who would like to image spermatozoan
motility. I am very comfortable doing live-cell imaging of mammalian
cells and tissue in culture on our inverted scope, but I'm assuming
there are specific issues of buffers and conditions to keep them
healthy. If you have experience imaging these, would you contact me
off-line?
I'm trying to avoid the word, to minimize the spam filtering.
Kathy
Kathryn Spencer, Ph.D.
The Scripps Research Institute
ICND 210
10550 N. Torrey Pines Road
La Jolla, CA 92037
(858) 784-8437
[hidden email]
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