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. 2018 Jul 11;8:10426. doi: 10.1038/s41598-018-28745-8

Figure 10.

Figure 10

Effect of rLOX-PP on FAK (Tyr397) and ERK (Thr202/Tyr204) phosphorylation induced by VEGF in HUVECs: (a) HUVECs were treated with rLOX-PP and vehicle ctrl. After treatment, cells were treated with 10 ng/mL of VEGF for 15 min. Whole cell extract were prepared and the samples were subjected to western blotting using antibodies against pFAK (Tyr397), total FAK, pERK (Thr202/Tyr204), total ERK and β–actin was used as loading control. The full-length blots are represented in Supplementary Figs 12, 13, 14, 15 and 16. (b) Bar graph represents the quantification of western blot using ImageJ software for pFAK (Tyr397) and (c) pERK (Thr202/Tyr204). (d) HUVECs were treated with rLOX-PP without stimulation of VEGF. Cell lysate were subjected to western blotting using pFAK (Tyr397), total FAK, pERK (Thr202/Tyr204), total ERK and β–actin. The full-length blots are represented in Supplementary Figs 12, 13, 14, 15 and 16. (e) Densitogram of the western blot shows the ratio of pFAK to total FAK, normalized with β-actin. (f) Densitogram of the western blot shows the ratio of pERK to total ERK, normalized with β-actin. Values were expressed as mean ± SD, n = 3. **p < 0.01, *p < 0.05 versus VEGF + Vehicle ctrl. #p < 0.05 versus CTRL. (CTRL – Control; Vehicle ctrl – Vehicle control).