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. 2012 Mar 14;7(3):e32977. doi: 10.1371/journal.pone.0032977

Figure 4. EMSA assays of the 173 bp intergenic region upstream of the yefM/yoeBsl operon with different proteins: (A) purified complex YefM/YoeB-His6sl (0, 1, 2 and 5 µM); (B) purified YefM-His6sl (0, 2, 4 and 8 µM); (C) Purified YoeB-His6sl (0, 1, 2, and 4 µM).

Figure 4

D) EMSA assays with in vitro reconstituted YefM-His6/YoeB-His6sl complexes. The absence or presence of YoeB-His6sl, and/or YefM-His6sl is indicated by −/+ respectively. 2 µM of YoeB-His6sl were used (lanes 3–7), and mixed with increasing amounts (1, 2, 4 and 8 µM) of YefM-His6sl (lanes 4–7). 1 µM of natural purified YefM/YoeB-His6sl complex was used as a control (lane 8). E) EMSA assays of different promoters from S. coelicolor (the SCO number is indicated) with (+) or without (−) 1 µM of the purified complex YefM/YoeB-His6 sl.