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Effect of LJE on intracellular lipid accumulation in HepG2 cells. Control (Con) cells were treated with 1% fat-free bovine serum albumin. (A) Oil Red O staining images of HepG2 cells (magnification 200×); (B) Quantitative Oil Red O contents at 500 nm; (C) Intracellular triglyceride contents were measured by fluorescence intensity. Data represent means ± SEM. ### p < 0.001 vs. Con; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. FFA.
