To help expand confirm the repressive aftereffect of the ZBRK1-binding theme for the MMP9 promoter, heterologous reporters generated by inserting a wild-type ZBRK1-binding theme, 1524/1497 oligonucleotides, or a mutated ZBRK1-binding theme, 1524/1497 oligonucleotides in to the pGL2-promoter vector, were useful for the reporter assay

To help expand confirm the repressive aftereffect of the ZBRK1-binding theme for the MMP9 promoter, heterologous reporters generated by inserting…