I have never tried for human cells, but just for mouse cells, the principle should be the same. If you want to stain the cells for IHC or IF the cells will be fixed and cut, so no particular problem, you can treat them as every other tissue. If you want to stain the fresh tissue/cell culture you can try fixing them with acetone: methanol 1:1 cold and then stain them with a normal IHC/IF protocol comprising the blocking step. If you want to stain the cells for flow cytometry, you could reactivate the cells (in the case they are not under stimuli) with a calcium stimulus (es 100ng/ml PMA and 1ug/ml Ionomycin 3h ) and then block the vescicular trafficking with brefeldin for 1 h (all in incubator). You can then use for example the Inside Stain kit from Miltenyi Biotec to mark first the surface antigens and then the intracellular antigens.
Thank you for your answer.I wasn't enough precise in my question. We have a protocole for immunofluorescence working for IL17 and we want to do now IFNg staining, but we can not find an IFNg antibody with convincing picture on human tissue. Does anyone known a good IFNg antibody for immunofluorescence on human tissue?