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. 2012 Jan;194(1):61–71. doi: 10.1128/JB.06143-11

Fig 5.

Fig 5

Runoff in vitro transcription assays with E. coli RNAP holoenzyme, using PvraSRL as a template (A), and E. coli RNAP haloenzyme, E. coli RNAP core enzyme, and S. aureus SigA in the presence of VraR-P, using PvraSRL as a template (B). The SigA concentrations in lanes 2 to 5 are 2, 4, 8, and 8 μM, respectively. The sizes of the transcription products were determined using the molecular weight marker φX174DNA/HinfI and the 160-bp DNA fragment (lane 1).