FIGURE 6.

Same efficiency of the extension of DNA and RNA primers on hetero-homopolymeric hybrid and heteropolymeric DNA templates by the p180ΔN-core. For control of the full extension of the primers, we used reactions with T4 DNA polymerase, which robustly and completely extended DNA as well as RNA primers (left lane in the left and right halves of the gel). Arrows show the zones of termination of DNA synthesis. All reactions contain 0.2 mm dNTPs, and the enzyme to primer/template ratio was 1:50, except for the T4 DNA pol (∼1:2500).