Hi Everyone, I typically used charged slides to mount my 50 um floating brain sections. However, these seem pricey and I remember subbing slides in the past. I most do DAB staining, native fluorescence and occasionally immunofluorescence. Can someone tell me a good and easy protocol for cleaning and subbing slides?
I currently have relatively old gelatin (7+ years?), Type B 225 bloom. Is this sufficient? A lot of protocols call for type A. Thanks! Caroline Bass University at Buffalo _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
