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. 2000 Feb;182(3):637–646. doi: 10.1128/jb.182.3.637-646.2000

FIG. 1.

FIG. 1

Affinity chromatography of FecR-(His)6 (A) and (His)10-FecR (B) on a Ni-NTA agarose column. The eluted fractions were subjected to SDS-PAGE (with 15% acrylamide gels) and stained with Coomassie brilliant blue. (C) Western blotting of Ni-NTA agarose column eluant fractions with anti-FecR serum. FecR-(His)6, (His)10-FecR, and their proteolytic cleavage products are indicated by arrows. Numbers indicate molecular masses in kilodaltons.