I'm having a problem with intense background noise in immunofluorescence for my biotinylated protein of interest conjugated with streptavidin (attached with a fluorophore) in mouse liver tissue (parafilm fixed/ frozen). This doesn't happen with bile duct tissue. I think the biotin or streptavidin is reacting with some liver-specific stuff, hence such a huge background.
Does anyone have any similar experience or a solution for this?