I co-transfected cell with reporter and effector plasmids and then sythesis cDNA using reporter plasmid specific primer to see the exogenous expression. In PCR reaction I used frward and rverse primer for specific exons to see the patterns of alternative splicing. The problem is that I also got PCR band in nontransfacted sample though the band is not so strong compared to the transfected cell. Could any one suggest me how to overcome this problem?