I use the technique of FISH (fluorescence in Situ Hybridation) to detect the
RNA of my complexe and I need to label a *nucleolus* for this reason I
follow my expirement of FISH by Immunofluoresence because I can't transforme
my cells with the plasmide which have my fluorescent protein.
So when I was using just the FISH I found good signal but when I used FISH
with Immunufluoresence I found that the signal strongly decreased.
I tried to do IF in the first and the FISH in the second but also the signal
of IF isn't good.
So I need if somebody was using this two techniques together in the yeast
please give me how did do
Thanks for your help
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