<p>L6 myotubes were starved for 2 hours in serum free high glucose DMEM containing 0.2%BSA followed by incubation for 2 h with 30 µM of BMS309403.</p
<p>Ncls treatment led to (A) increased phospho-AMPKα (pAMPKα), increased phospho-ACC2 (pACC2), and (...
<p>The cells were then lysed with lysis buffer, and the phosphorylation of AMPKα was assessed by wes...
<p>BMDMs were cultured in the presence of different concentrations of A-769662 for 2 hours (A), or B...
<p>C2C12 myotubes were starved for 2 hours in serum free high glucose DMEM containing 0.2%BSA follow...
<p>C2C12 myotubes were starved for 2 hours in serum free high glucose DMEM containing 0.2% BSA follo...
<p>(a) Indicated agents were treated for 5 min and 5 µM concentration with or without 30 min pre-inc...
<p>C2C12 myotubes were pretreated with compound C (C.C) for 30 min followed by the addition of BMS30...
<p>(A) Differentiated L6 cells were treated with MES (0.1 ms, 1 V/cm, 55 pps) for 10 min. Cell lysat...
<p><b>A</b> AMPK Thr<sup>172</sup>-phosphorylation in L6 myoblast after stimulation with 1μM compoun...
<p>(a) L6 myotubes were pre-incubated with the AMPK chemical inhibitor, compound c, for 30 min and t...
<p>L6 myotubes were transfected with vehicle, unrelated siRNA or AMPKα1/2 siRNA as described in Rese...
<p>Western blotting analysis of AMPK phosphorylation in C2C12 myobubes overexpressing FABP3 with or ...
<p>This is a representative blot from three individual experiments. The density of the bands were qu...
<p>(A,B) BMDMs were pre-treated with A-769662 (100, 250 or 500 μM) for 2 hours before stimulated wit...
Additional file 1: Figure S1. EXE induced AMPKα activation and 2DG-uptake in cultured L6 myotubes. M...
<p>Ncls treatment led to (A) increased phospho-AMPKα (pAMPKα), increased phospho-ACC2 (pACC2), and (...
<p>The cells were then lysed with lysis buffer, and the phosphorylation of AMPKα was assessed by wes...
<p>BMDMs were cultured in the presence of different concentrations of A-769662 for 2 hours (A), or B...
<p>C2C12 myotubes were starved for 2 hours in serum free high glucose DMEM containing 0.2%BSA follow...
<p>C2C12 myotubes were starved for 2 hours in serum free high glucose DMEM containing 0.2% BSA follo...
<p>(a) Indicated agents were treated for 5 min and 5 µM concentration with or without 30 min pre-inc...
<p>C2C12 myotubes were pretreated with compound C (C.C) for 30 min followed by the addition of BMS30...
<p>(A) Differentiated L6 cells were treated with MES (0.1 ms, 1 V/cm, 55 pps) for 10 min. Cell lysat...
<p><b>A</b> AMPK Thr<sup>172</sup>-phosphorylation in L6 myoblast after stimulation with 1μM compoun...
<p>(a) L6 myotubes were pre-incubated with the AMPK chemical inhibitor, compound c, for 30 min and t...
<p>L6 myotubes were transfected with vehicle, unrelated siRNA or AMPKα1/2 siRNA as described in Rese...
<p>Western blotting analysis of AMPK phosphorylation in C2C12 myobubes overexpressing FABP3 with or ...
<p>This is a representative blot from three individual experiments. The density of the bands were qu...
<p>(A,B) BMDMs were pre-treated with A-769662 (100, 250 or 500 μM) for 2 hours before stimulated wit...
Additional file 1: Figure S1. EXE induced AMPKα activation and 2DG-uptake in cultured L6 myotubes. M...
<p>Ncls treatment led to (A) increased phospho-AMPKα (pAMPKα), increased phospho-ACC2 (pACC2), and (...
<p>The cells were then lysed with lysis buffer, and the phosphorylation of AMPKα was assessed by wes...
<p>BMDMs were cultured in the presence of different concentrations of A-769662 for 2 hours (A), or B...