posted on 2015-03-10, 02:57authored byNami Kim, Hong Min Kim, Eun Soo Lee, Jung Ok Lee, Hye Jeong Lee, Soo Kyung Lee, Ji Wook Moon, Ji Hae Kim, Joong Kwan Kim, Su Jin Kim, Sun Hwa Park, Choon Hee Chung, Hyeon Soo Kim
The green fluorescent signal was detected using confocal microscopy. (B) C2C12 cells pre-treated with STO-609, a CaMKK inhibitor, for 30 min and then treated with 30 μM DBM for 1 h. The cells were then lysed with lysis buffer, and the phosphorylation of AMPKα2 was assessed by western blot using phosphorylation-specific antibodies. The level of total AMPKα2 was also assessed as a control for protein loading. * p < 0.05, as compared with basal condition. (C) Myoblast L6 cells were differentiated for 7 days and then pre-treated with STO-609 (1 μM) and then DBM (30 μM) for 1 h. Glucose uptake was then assayed for 2-DG uptake as described in the Methods. *p < 0.05, compared with control. **p < 0.05, compared with DBM-treated cells.