[Histonet] Fluorescence staining
We are looking into trying some Fluorescence staining. We want to try a
TSA Fluorescence System from PerkinElmer. The IHC protocol does however
leave me with some questions.
We always dehydrate our samples after staining. The protocol however
doesn't mention this. It only says that the samples can be
counterstained and mounted after incubation with the Fluorophore
Tyramide. Should we dehydrate and is there a particular mounting media
we should use to prolong the time that fluorescence can be detected? Any
help would be greatly appreciated.
Thanks in advance for all your help,
Histonet mailing list
<< Previous Message | Next Message >>