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. 2016 Aug 10;7(36):58405–58417. doi: 10.18632/oncotarget.11168

Figure 4. GHK-Cu suppressed the activation of the p38 MAPK signaling pathway in LPS-induced RAW 264.7 cells activation.

Figure 4

A. Western blotting was performed using a specific antibody for the detection of the phosphorylation of p38 MAPK, JNK1/2, and ERK1/2. p38 MAPK, JNK1/2, and ERK1/2 were used as loading controls. B. The blots were subjected to a densitometric analysis and relative quantification. The values are the means ± SD after normalization for p38 MAPK, JNK1/2, and ERK1/2 (n = 3). A representative blot is shown for each condition. *p < 0.05, statistically significant difference. CTL, control.