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. 2003 Jan;185(2):688–692. doi: 10.1128/JB.185.2.688-692.2003

FIG. 3.

FIG. 3.

Gel mobility shift assays of NACWT or NACNC with the full-length gdhA promoter. Increasing amounts of purified NACWT-his (lanes 2 to 7) or NACL111K-his (lanes 8 to 13) were incubated with 128 nM DNA fragment containing both NAC-binding sites. Lanes 1 to 7 contained 0, 25, 50, 75, 100, 125, and 150 nM active NACWT-his, respectively. Lanes 8 to 13 contained 150, 125, 100, 75, 50, and 25 nM NACL111K-his, respectively.