Gel-shift assay following incubation of 0.1 μM 291bp-PCR fragment with PM (lanes 1-8), MM1 (lane 9) and MM2 (lane 10) binding site with different concentrations of γPNAs (γPNA4, lanes 2 & 3; γPNA5, lanes 5, 6, 9 & 10; γPNA3 + γPNA5, lane 8) and PNAs (PNA4, lane 4; PNA5, lane 7) under identical condition as denoted in . γPNA4 and γPNA5 were designed to bind to the top strand of the PM, MM1 and MM2 target. γPNA3 and γPNA5 are complementary to one another.