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. 2010 Sep 27;39(3):1042–1053. doi: 10.1093/nar/gkq786

Figure 4.

Figure 4.

The clamp/polymerase activity of different RTs and DNA polymerases. All enzymes (with equal DDDP activities, tested by a DNA–primer extension assay, see Supplementary Figure S1) were incubated with the indicated substrate as described in ‘Materials and Methods’ section. MLV RT was assayed with 5 mM MgCl2 or 0.8 mM MnCl2 while Tf1 RT with 5 mM MgCl2 or 0.5 mM MnCl2. All other enzymes were assayed with 5 mM MgCl2. Lane 1, T/P only; lanes 2–21, reactions with the various enzymes, in the absence (even-numbered lanes) or the presence of dNTPs (odd-numbered lanes). The different RTs/DNA polymerases and the presence of Mn+2 or Mg+2 (for MLV and Tf1 RTs) are indicated. (A) Assayed with set #1. (B) Assayed with set #2.