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. 2017 Apr 6;26(2):157–166. doi: 10.4062/biomolther.2016.234

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Copyright © 2018 The Korean Society of Applied Pharmacology

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 7. — Effect of diosmetin on Nrf2/HO-1 pathway in vitro. (A, B) RAW264.7 and A549 cells were treated with diosmetin (40 μM) for the indicated time, and then the cells were collected. Protein expression of Nrf2 and HO-1 in total cell lysates was determined by western blot in RAW264.7 (A) and A549 (B) cells. (C, D) Densitometry quantitation of protein expression in RAW264.7 (C) and A549 (D) cells. β-actin acted as an internal control. Data was expressed as means ± SEM. n=5. ^**p<0.01 vs the control group.