Hi Everyone, I am still having issues with my IHCs with Acetone fixation.
If I fix in 100% Acetone, I get IHC staining, but my tissues are 50-90% destroyed. If I fix in 4% paraformaldehyde, or 10% NBF or (95% Etoh and/or Methanol with Acetone) I lose the epitopes I either get no staining or very weak staining, but the tissue morphology look fine. I just tried an acetone gradient where I cut the tissues at 5 uM and dried them overnight, then fixed for 10 minutes in 100% acetone, then fixed in 95% acetone for 1 minute, then fixed in 70% acetone for 30 seconds, then quick rinsed in H20, then washed as normal in DPBS pH 7.4. I did 4 slides, 2 slides with one company's Charged slides ,and 2 slides with another company's charged slides. One company's slides look completely destroyed, the others may turn out, it was hard to tell how much damage there was. I'll know tomorrow when I finish staining and Hemotoxylin them. Patrick Lewis Research Associate II Bench Seattle Childrens Research Institute 206-884-1115 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 protected by law. 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. _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
