I am looking at DNA staining of human sperm by flow and have seen completely different propidium iodide staining patterns with two different decondensation protocols. Any advice about optimizing sperm chromatin decondensation and denaturation would be greatly appreciated; especially, in the context of flow FISH or FISH in suspension. Thanks, Annie Bang. MOUNT SINAI SERVICES Annie Bang Flow Cytometry Centre Pathology and Laboratory Medicine Mount Sinai Hospital Room 6-209 600 University Avenue Toronto, Canada M5G 1X5 Phone (1) (416) 586 4800 ext 6530 Fax (1) (416) 586 8628 E-mail abang@mtsinai.on.ca <mailto:kpritzker@mountsinaiservices.com> Confidentiality Notice: This e-mail message, including any attachments, is for the sole use of the intended recipient(s) and may contain confidential and privileged information. Any unauthorized review, use, disclosure or distribution is prohibited. If you are not the intended recipient, please contact the sender by reply e-mail and destroy all copies of the original message.Received on Thu May 1 10:18:00 2008
This archive was generated by hypermail 2.1.8 : Wed Jan 31 2007 - 03:12:00 EST