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. 2017 Feb 16;8(12):20042–20055. doi: 10.18632/oncotarget.15373

Figure 10. A. Effects of H2O2 on NF-κB activation after silencing of TLR4 in RAW264.7 cells.

Figure 10

Phosphorylation levels of p65 and IκBα were determined by western blotting after knockdown of TLR4 using siRNA or thymol, NAC pre-treatment. β-actin serves as an internal control. B. Translocation of NF-κB p65 in TLR4-si RAW264.7 cells challenged with LPS as assessed using immunofluorescence. C. Expression of the cytokines, IL-1β and TNF-α, was detected using qPCR. GAPDH served as a control. CG indicates the control group. LPS indicates the LPS-stimulated group. TLR4-si indicates the TLR4 siRNA group. NAC indicates the N-acetyl cysteine group. The white arrow indicates the translocation of p65. Data represent the mean ± S.E.M. of three independent experiments. #p<0.01 vs. Control group. *p<0.05 vs. LPS group, **p<0.01 vs. LPS group.