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. Author manuscript; available in PMC: 2009 Aug 15.
Published in final edited form as: Life Sci. 2008 Jun 28;83(7-8):293–300. doi: 10.1016/j.lfs.2008.06.017

Figure 5.

Figure 5

Electrophoretic mobility shift assay (EMSA) showing the DNA binding activity of NF-κB in nuclear protein fractions from untreated (control), isoflavone-, curcumin-, or isoflavone + curcumin-treated BxPC-3 and Colo-357 cells. Super-shift assay showed that NF-κB band was shifted because of the formation of bigger complex after addition of anti- NF-κB p65 antibody. This assay confirmed the specificity of NF-κB binding to the DNA consensus sequence.