I'm trying to delete a gene in primary bone marrow derived macrophages from a flox/flox mouse. I can get the Adeno-GFP to work very well (fluoresce green), but the Adeno-Cre-GFP is not showing up?
Could you please add some more detail? Does you cloning procedure result in an in frame Cre-GFP fusion product? are there any sort of "IRES" or "2A peptide" sequences located between the CRE and GFP coding sequences? Is the CRE expression induced conditionally?
For your cloning experiment if you used a commercial Cre-GFP expression plasmid, use it first as a control of Cre-GFP expression and check what Farbod said.