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E01-GS-TPD inhibits A431 cell migration. Scratches were made in confluent A431 cultures to create a visible wound in the cell monolayer. Cultures were treated with recombinant protein at a final concentration of 0.5 µM for 24 h and the remaining wound area was compared to the initial wound at 0 h (a). The remaining wound area for each condition was then calculated to determine the effects of each protein on cell migration (b). Mean and standard deviation from n = 2 is shown.
