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Effect of SA on the expression of osteoblast differentiation marker genes and Osterix. mMSCs were treated with SA at 150 μM in DMEM media for 14 d. Total RNA was isolated and subjected to RT-qPCR analysis using the primers for (A) ALP, (B) Col-I, (C) OC and (D) Osterix genes. RPL13A was used as an internal control for normalization. *indicates a significant increase compared to control (p < 0.05)
