<p>EL4 T cells were incubated in DMEM medium with an immobilized anti-CD3/CD28 mAb in the presence or absence of si-OCILRP2. After incubation at 37°C for 48 h, the T cells were lysed, and aliquots of 20 µg of the whole-cell lysate were analyzed by western blotting using antibodies against phospho-Erk, Erk, phospho-Jnk, and Jnk (a) and phospho-Raf and phosphor-Akt (b). The data are expressed as a percentage of the level of active Erk or Jnk of the total Erk or Jnk. Each data point represents the mean ± S.E. from three separate experiments.</p
<p>A: Western blots to detect phosphorylated JNK and total JNK expression. Ratio of phosphorylated J...
<p>Extracts from DP thymocytes, column-purified mature T cells (T) and anti-CD3/CD28 stimulated T ce...
<p>LaminB1 was used to ensure equal sample loading. <b>Low panels.</b> Densitometric analysis of at ...
<p>Western blot analyses of protein extracts from CD3<sup>+</sup> T cells stimulated with immobilize...
<p>Representative immunoblots and densitometric analysis of (A) phosphorylated Akt (p-Akt) and total...
<p>The upper side of panel (A) shows a representative Western blot for Phospho-p44/42 MAPK (Erk1/2) ...
<p><b>Panel A.</b> Western blot analysis of total protein extracts from CD4+ T cells stimulated with...
<p>Phosphorylation of ERK1/2 in 293T cells transfected with empty vector, FSHRwt, FSHRmt, or FSHRwt/...
<p>Cells were pre-treated with NO-Cbl (300 µM, 16 h) followed by doxorubicin (20 µM, 4 h) or cisplat...
<p>(A) Three samples of Jurkat E6.1 T cells, HuT78 T cells, and APBTs were stimulated and the cellul...
<p>(<b>A</b>) LbetaT2 cells were starved overnight in serum-free DMEM and then treated by 10 nM WT, ...
<p>(<b>A</b>) AKR-2B and NIH 3T3 fibroblast were treated with TGF-β (2 ng/ml) for times ranging from...
<p>Phospho-Akt and phospho-Erk detected by western blot of cell lysates from MCF-7 and SKBR-3 cells ...
<p>Neutrophils were stimulated with C5a 100 ng/ml or buffer for 15 min followed by stimulation with ...
<p>Cells were incubated with GrK (200 nM) for 10 min, 30 min, or 2 h. Cell lysates were collected an...
<p>A: Western blots to detect phosphorylated JNK and total JNK expression. Ratio of phosphorylated J...
<p>Extracts from DP thymocytes, column-purified mature T cells (T) and anti-CD3/CD28 stimulated T ce...
<p>LaminB1 was used to ensure equal sample loading. <b>Low panels.</b> Densitometric analysis of at ...
<p>Western blot analyses of protein extracts from CD3<sup>+</sup> T cells stimulated with immobilize...
<p>Representative immunoblots and densitometric analysis of (A) phosphorylated Akt (p-Akt) and total...
<p>The upper side of panel (A) shows a representative Western blot for Phospho-p44/42 MAPK (Erk1/2) ...
<p><b>Panel A.</b> Western blot analysis of total protein extracts from CD4+ T cells stimulated with...
<p>Phosphorylation of ERK1/2 in 293T cells transfected with empty vector, FSHRwt, FSHRmt, or FSHRwt/...
<p>Cells were pre-treated with NO-Cbl (300 µM, 16 h) followed by doxorubicin (20 µM, 4 h) or cisplat...
<p>(A) Three samples of Jurkat E6.1 T cells, HuT78 T cells, and APBTs were stimulated and the cellul...
<p>(<b>A</b>) LbetaT2 cells were starved overnight in serum-free DMEM and then treated by 10 nM WT, ...
<p>(<b>A</b>) AKR-2B and NIH 3T3 fibroblast were treated with TGF-β (2 ng/ml) for times ranging from...
<p>Phospho-Akt and phospho-Erk detected by western blot of cell lysates from MCF-7 and SKBR-3 cells ...
<p>Neutrophils were stimulated with C5a 100 ng/ml or buffer for 15 min followed by stimulation with ...
<p>Cells were incubated with GrK (200 nM) for 10 min, 30 min, or 2 h. Cell lysates were collected an...
<p>A: Western blots to detect phosphorylated JNK and total JNK expression. Ratio of phosphorylated J...
<p>Extracts from DP thymocytes, column-purified mature T cells (T) and anti-CD3/CD28 stimulated T ce...
<p>LaminB1 was used to ensure equal sample loading. <b>Low panels.</b> Densitometric analysis of at ...