Figure 1.
Figure 1. Binding of USF1 and USF2 to the TME in HEL cells. (A) Detection of USF1 and USF2 among the TME binding proteins. Western blotting was performed with fractions from a DNA affinity column. Fraction numbers of affinity column elute are indicated above. *Faint USF1 band. TME binding activity of each fraction was measured by EMSA. (B-C) Detection of USF1 and USF2 in the TME binding complex in HEL cells by the supershift assay. A supershift assay was performed with nuclear extracts of HEL cells and factor-specific antibodies. Arrow indicates supershifted band. The TME probe (B) or TMEmut probe (C) that includes the mutations in the E-box motifs was used. (–) indicates no antibody.

Binding of USF1 and USF2 to the TME in HEL cells. (A) Detection of USF1 and USF2 among the TME binding proteins. Western blotting was performed with fractions from a DNA affinity column. Fraction numbers of affinity column elute are indicated above. *Faint USF1 band. TME binding activity of each fraction was measured by EMSA. (B-C) Detection of USF1 and USF2 in the TME binding complex in HEL cells by the supershift assay. A supershift assay was performed with nuclear extracts of HEL cells and factor-specific antibodies. Arrow indicates supershifted band. The TME probe (B) or TMEmut probe (C) that includes the mutations in the E-box motifs was used. (–) indicates no antibody.

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