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. Author manuscript; available in PMC: 2014 Jul 7.
Published in final edited form as: Biol Psychiatry. 2009 May 7;66(3):214–222. doi: 10.1016/j.biopsych.2009.02.033

Fig. 5.

Fig. 5

Specific binding of Freud-2 to human DRE sequences. Electrophoretic mobility shift assay (EMSA) was done using bacterially expressed purified recombinant GST-Freud-2 fusion protein (GST-hF2) or GST alone with labelled 5′or 3′DRE from the human 5-HT1A promoter. For competition, unlabelled 5′or 3′DRE (cold) were used at 100-fold molar excess. Antibody to GST (GST-Ab, 2 μl/sample) was added as indicated. A single band (arrow) was detected which was competed with excess unlabeled 5′ or 3′ DRE, indicating that Freud-2 protein binds both 5′ and 3′ DRE from human 5-HT1A promoter.