Dear all,
I am sure this has been discussed here before but I am new to this place and
would appreciate your help. I would like to know how stable GFP fluorescence is
in respect to standard histological and cytological techniques, specifically
various fixatives (formalin, ethanol, acetic acid...) and e.g. drying of
sections on the slide or dehydration through alcohol and xylene, peroxidase
reactions, AP reactions.... What are the DON'Ts and DOs? Is there a concise
source of information (maybe an archive of this list)? Please reply to me
directly as I don't regularly read this list. If I get useful tips, I will post
a summary to the list.
Thank you very much,
Christian
Brain Research Institute
University of Zurich
Switzerland
