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. 2012 Nov 12;17(11):13424–13438. doi: 10.3390/molecules171113424

Figure 5.

Figure 5

The effect of ISL on p47phox and gp91phox expression in HL-60 cells. (A) Cells were treated with ISL (0, 2.5, 5, or 10 μg/mL) for 72 h, and protein was extracted rapidly for Western blot analysis. β-Actin was used as the internal control. (B) The levels of p47phox and gp91phox mRNA expression in ISL-treated HL-60 cells. GAPDH was used as an internal control.