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. 2010 Sep 9;285(46):35340–35349. doi: 10.1074/jbc.M110.156836

FIGURE 8.

FIGURE 8.

RanBPM inhibits Mgl-1 cell migration. A, stably transfected MDCK cells with respective constructs were checked for Mgl-1-mediated migratory and invasive potential by wound healing assays. Images were captured at a time interval between 0 and 16 h. Assays were performed in triplicate. B, percentage of migration was statistically analyzed from three separate experiments. n = 3. *, p < 0.05. C, stably transfected MDCK cells with empty vector, RanBPM, RanBPMΔSPRY, RanBPM shRNA1, and RanBPM shRNA2 were analyzed for endogenous Mgl-1 cell migration by wound healing assay. D, percentage of migration was statistically analyzed from three separate experiments. n = 3. *, p < 0.05.