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. 2000 Jan;182(1):14–22. doi: 10.1128/jb.182.1.14-22.2000

FIG. 6.

FIG. 6

Gel retardation experiments with purified B. japonicum HrcA. DNA-binding reactions were performed with DNA fragments derived from the promoter region of groESL5 (A) and groESL4 (A, C, and D). (B) groESL4 fragments represented schematically. CIRCE4* represents a DNA fragment in which the CIRCE element was mutated (see Materials and Methods). The amount of H6-HrcA used is indicated above each lane in all panels. The positions of radiolabeled free DNA (f) and retarded bands (r) are marked.