When Hodgkin slides are fixed with DAPI counterfade we are seeing excellent uptake on the small lymphocytes but extremely patchy HRS nuclear staining. Improving this could help with out analysis.
I had problems with a patchy Hoechst stain, but I redid the staining with the inclusion of 0.01% triton X-100. The results were great, maybe this can help you.
Triton is good at permeabilising cells allowing the nuclear label to enter the cells. However, sometimes certain cells tend to wash of and if this is the case another permeabilising reagent such as methanol or acetone can be used.