Fig. 4.
Fig. 4. Transcription factor binding and transactivation capacity of the κB site of β2m. / (A) EMSA showing binding of complexes to the κB site of β2m. Using specific Abs, the complex binding to the κB was shown to contain p50 and p65. The presence of c-Rel and RelB was weakly detectable in Raji and MSH B cells. Note the difference in the quantity of complex formation with an equal loading as in Figure3. Arrowheads indicate NF-κB complexes binding the κB site; *, supershifted complex(es). (B) Transient transfection of wild-type β2m- and κB site–mutated reporter constructs with p50 and p65 expression vectors (1 μg) in Tera-2 cells. The luciferase activity values were normalized with the Renilla luciferase activity values and are expressed as mean ± SD of 4 samples. The induction ratios are indicated above the histogram. RLU indicates relative light units.

Transcription factor binding and transactivation capacity of the κB site of β2m.

(A) EMSA showing binding of complexes to the κB site of β2m. Using specific Abs, the complex binding to the κB was shown to contain p50 and p65. The presence of c-Rel and RelB was weakly detectable in Raji and MSH B cells. Note the difference in the quantity of complex formation with an equal loading as in Figure3. Arrowheads indicate NF-κB complexes binding the κB site; *, supershifted complex(es). (B) Transient transfection of wild-type β2m- and κB site–mutated reporter constructs with p50 and p65 expression vectors (1 μg) in Tera-2 cells. The luciferase activity values were normalized with the Renilla luciferase activity values and are expressed as mean ± SD of 4 samples. The induction ratios are indicated above the histogram. RLU indicates relative light units.

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