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Effect of CAt extract treatment on AKT, ERK, and p38 protein expression in HepG2 and Mahlavu cells. HepG2 and Mahlavu cells were incubated with CAt extract (25 or 30 μg/mL) for the indicated time points (0, 6, 12, 24, and 48 h) then subjected to Western blotting analysis. The actin level was used as loading control. †: Significant difference between control and treatment, p < 0.05.
