<p>The effect of EPO on p-Akt was determined. H9C2 cells (A) were subjected to 8 hrs hypoxia and 30 mins of reperfusion with or without pre-treatment with 20 U/ml EPO and 1 µM Wortmannin before 30 mins for 24 hrs and stained with p-AKT antibody. EPO increase p-Akt. (B) Represents the quantification green florescence, which indicates the increase in levels of p-Akt. Data are presented as means ± SEM of the ratios from three independent experiments * denotes p<0.001 for analyses compared to H/R.</p
<p><b>A</b>] Cell surface EPOR detection using antibody EC-c38.5 – Among rabbit monoclonal antibodie...
<p>Changes in phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells trea...
: Erythropoietin (EPO) has both erythropoietic and tissue-protective properties. The EPO analogues c...
<p>The effect of EPO on p-Akt was determined using Western blot. H9C2 cells were <sup>i</sup>subject...
<p>The effect of EPO on cell viability was determined using MTT assay. H9C2 cells were subjected to ...
<p>The effect of EPO on caspase-3 activity was determined using caspase-3 colorimetric assay. H9C2 c...
<p>The effect of EPO on intracellular calcium and MPTP opening was determined using time–lapse imagi...
<p>The effect of EPO on apoptosis and necrosis was determined using Acridine/Orange (Ao/EtBr) double...
<p>(<b>A</b>) Western blot analysis was performed for phosphorylated (p-)-PRAS40 (p-PRAS40, Thr<sup>...
<p>The effect of EPO on Membrane potential was determined by colocalization studies using Rhodamine-...
<p>ARPE-19 cells were treated with Epo (0.3∼10 nM) (<b>A</b>) or LA (100–1000 nM) (<b>B</b>) for 18–...
<p>(A) RCC cells were treated with 0–100 U/ml Epo for 5 min after serum starvation for 24 hours. Com...
<p>Immunofluorescence (A), Real-time PCR (B) and Western blot analysis (C) demonstrated that ephrin-...
<p>(A) NCI-H838 cells were serum and Epo-starved overnight in medium containing 0.1% serum then trea...
<p>(A) WT or Akt DKO MEF cells were subjected to normoxia (C) or hypoxia (0.1%±0.1 O<sub>2</sub>) (H...
<p><b>A</b>] Cell surface EPOR detection using antibody EC-c38.5 – Among rabbit monoclonal antibodie...
<p>Changes in phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells trea...
: Erythropoietin (EPO) has both erythropoietic and tissue-protective properties. The EPO analogues c...
<p>The effect of EPO on p-Akt was determined using Western blot. H9C2 cells were <sup>i</sup>subject...
<p>The effect of EPO on cell viability was determined using MTT assay. H9C2 cells were subjected to ...
<p>The effect of EPO on caspase-3 activity was determined using caspase-3 colorimetric assay. H9C2 c...
<p>The effect of EPO on intracellular calcium and MPTP opening was determined using time–lapse imagi...
<p>The effect of EPO on apoptosis and necrosis was determined using Acridine/Orange (Ao/EtBr) double...
<p>(<b>A</b>) Western blot analysis was performed for phosphorylated (p-)-PRAS40 (p-PRAS40, Thr<sup>...
<p>The effect of EPO on Membrane potential was determined by colocalization studies using Rhodamine-...
<p>ARPE-19 cells were treated with Epo (0.3∼10 nM) (<b>A</b>) or LA (100–1000 nM) (<b>B</b>) for 18–...
<p>(A) RCC cells were treated with 0–100 U/ml Epo for 5 min after serum starvation for 24 hours. Com...
<p>Immunofluorescence (A), Real-time PCR (B) and Western blot analysis (C) demonstrated that ephrin-...
<p>(A) NCI-H838 cells were serum and Epo-starved overnight in medium containing 0.1% serum then trea...
<p>(A) WT or Akt DKO MEF cells were subjected to normoxia (C) or hypoxia (0.1%±0.1 O<sub>2</sub>) (H...
<p><b>A</b>] Cell surface EPOR detection using antibody EC-c38.5 – Among rabbit monoclonal antibodie...
<p>Changes in phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells trea...
: Erythropoietin (EPO) has both erythropoietic and tissue-protective properties. The EPO analogues c...