Hi all, I am in the process of validating DIF on derm samples and am wondering if anyone in the group can share what type of controls they used to validate this testing. Also, what is the best way to freeze your samples? Snap freeze or the routine slower method in the cryostat.
Thanks in advance for your help. Paula _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
