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Figure 3 Figure 3. Effect of complex C1 on PANC-1 cell’s migratory potential. Cells were treated with DMSO or 1 µM complex C1, and scratch was made on 100% confluent cells in Petri dish. Gap was captured and measured after 0 h and 24 h (representative images are presented in upper panel). Cell migration was determined in 24 h time point by calculating percentage of wound closure compared to the gap width at 0 h that was set as 100%. Results were presented as the means ± SEM of at least three independent experiments. Student’s t-test was used to calculate p-values (* p ≤ 0.05).
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