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. 2009 Feb 13;106(9):3467–3472. doi: 10.1073/pnas.0810291106

Fig. 3.

Fig. 3.

NepR forms a complex with σEcfG1. (A) Elution profile of purified σEcfG1 and NepR (4 μM) analyzed separately by gel filtration using a Superdex 75 10/300 column (flow rate, 0.5 mL/min). (B) Mixture of equimolar of each protein (8 μM each) led to the formation of a heterodimeric complex of σEcfG1 and NepR. Fractions were collected and analyzed on a 15% SDS-polyacrylamide gel and silver stained. The exact elution volume is indicated above the absorption peak.