To whom it may concern, I recently started trying to do flowcytometry on primary human colon cancer cells. I obtain the tissue and then generate a single cell suspension. My viability prior to fax is apprx.50%-60% (tyrpan blue). However, my facs data is showing viability in the 1-2%? I was wondering if anyone has any recommendations or advice for me on isolating primary human colon cancer cells and carrying out facs on these cells ? Thank you, Catherine O'Brien University of Toronto This e-mail may contain confidential and/or privileged information for the sole use of the intended recipient. Any review or distribution by anyone other than the person for whom it was originally intended is strictly prohibited. If you have received this e-mail in error, please contact the sender and delete all copies. Opinions, conclusions or other information contained in this e-mail may not be that of the organization.Received on Tue Oct 5 13:18:00 2004
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