wolfsc at ibms.sinica.edu.tw
Fri Jun 1 02:00:41 EST 2001
When you remove H89, will the cells re-attach again?
Are you working with coated coverslips or are they pure glass?
If you should need collagen or something, Kathrin and Cora in
B2 should have some solution and protocols (and even the
vacuum exsiccator that you'll need for the procedure).
How do things go in Tuebingen?
Viele Gruesse aus TaiPei,
From: mnwoznia at med.uni-tuebingen.de (Marcin)
Subject: H89 inhibitor
Date sent: 31 May 2001 10:58:19 +0100
Organization: BIOSCI/MRC Human Genome Mapping Project Resource Centre
Originally to: methods at net.bio.net
To: methods at hgmp.mrc.ac.uk
> Dear all,
> I'm trying to use H89 - a PKA specific inhibitor on transfected and
> untransfected NIH3T3 cells. I added 5ul of 10mM DMSO solution to 1ml of
> medium to reach the final concentration of 50uM. Unfortunately almost all
> the cells swim away after 30 min, and I'm not able to fix them on glass
> Do you have any hints?
> I would greatly appreciate any help,
[tiss mezzage wahs broduceRd using TYPO GENERATOR zoffwer]
Dr. Wolfgang Schechinger
Lab N233 (c/o Dr. Steve Roffler)
Institute of Biomedical Sciences
128 Yen-Chio Yuan Rd. Sec.2
wolfsc at REMOVETHESEANTISPAMCAPITALSibms.sinica.edu.tw
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