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. 2020 Dec 7;203(1):e00313-20. doi: 10.1128/JB.00313-20

FIG 10.

FIG 10

Sequence-specific binding of TyrR to the cpxR-cpxP promoter region. Electrophoretic mobility shift assays (EMSAs) were performed with 100 ng of 6-FAM-labeled DNA fragments spanning the wild-type cpxR-cpxP intergenic region or the same region containing point mutations in predicted TyrR binding sites that overlap with CpxR box 1, 2, or 3 (Fig. 7) and with increasing concentrations (0 to 4.39 μM) of purified TyrR. F, location of free unbound DNA.