anti phospho insulin receptor β Search Results


94
Cell Applications Inc phosphorylated ir
Phosphorylated Ir, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc antiphospho igf ir rabbit polyclonal antibody tyr1131
FIGURE 2. Modulation of <t>IGF/IGF-IR</t> signaling caused by knockdown of IGFBP-2. The IGFBP-2-knockdown cells (IGFBP-2 KD) and control cells were treated with the indicated concentrations of IGF-I or IGF-II in serum-free con- dition, and extents of phosphorylation of IGF-IR (p-IGF-IR), Akt (p-Akt), and ERK1/2 (p-Erk1/2) were analyzed by immunoblot and a representative result of U251 was shown. The band intensity was measured and the ratio of phos- phorylated protein to the corresponding total protein was calculated.
Antiphospho Igf Ir Rabbit Polyclonal Antibody Tyr1131, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
Boster Bio igf 1
FIGURE 2. Modulation of <t>IGF/IGF-IR</t> signaling caused by knockdown of IGFBP-2. The IGFBP-2-knockdown cells (IGFBP-2 KD) and control cells were treated with the indicated concentrations of IGF-I or IGF-II in serum-free con- dition, and extents of phosphorylation of IGF-IR (p-IGF-IR), Akt (p-Akt), and ERK1/2 (p-Erk1/2) were analyzed by immunoblot and a representative result of U251 was shown. The band intensity was measured and the ratio of phos- phorylated protein to the corresponding total protein was calculated.
Igf 1, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biorbyt p insulin receptor
FIGURE 2. Modulation of <t>IGF/IGF-IR</t> signaling caused by knockdown of IGFBP-2. The IGFBP-2-knockdown cells (IGFBP-2 KD) and control cells were treated with the indicated concentrations of IGF-I or IGF-II in serum-free con- dition, and extents of phosphorylation of IGF-IR (p-IGF-IR), Akt (p-Akt), and ERK1/2 (p-Erk1/2) were analyzed by immunoblot and a representative result of U251 was shown. The band intensity was measured and the ratio of phos- phorylated protein to the corresponding total protein was calculated.
P Insulin Receptor, supplied by Biorbyt, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biorbyt anti pd l1
FIGURE 2. Modulation of <t>IGF/IGF-IR</t> signaling caused by knockdown of IGFBP-2. The IGFBP-2-knockdown cells (IGFBP-2 KD) and control cells were treated with the indicated concentrations of IGF-I or IGF-II in serum-free con- dition, and extents of phosphorylation of IGF-IR (p-IGF-IR), Akt (p-Akt), and ERK1/2 (p-Erk1/2) were analyzed by immunoblot and a representative result of U251 was shown. The band intensity was measured and the ratio of phos- phorylated protein to the corresponding total protein was calculated.
Anti Pd L1, supplied by Biorbyt, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc phospho tyr1150 1151 insulin receptor ins
Fold change of phosphorylation status and total protein content pre‐ to post‐exercise of <t>INSR</t> <t>Tyr1150/1151</t> , Akt Ser473 , AS160 Thr642 , GLUT4, AMPK Thr172 , ACC Ser79 , PDK4, PDH Ser293 and HSL Ser660 ( B ) with representative blots ( A ). Data shown as the mean ± SD. Differences between FAST vs . CARB and CARB vs . NIACIN assessed using a paired t test ( n = 8 males).
Phospho Tyr1150 1151 Insulin Receptor Ins, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio rabbit anti human igf ir
Fold change of phosphorylation status and total protein content pre‐ to post‐exercise of <t>INSR</t> <t>Tyr1150/1151</t> , Akt Ser473 , AS160 Thr642 , GLUT4, AMPK Thr172 , ACC Ser79 , PDK4, PDH Ser293 and HSL Ser660 ( B ) with representative blots ( A ). Data shown as the mean ± SD. Differences between FAST vs . CARB and CARB vs . NIACIN assessed using a paired t test ( n = 8 males).
Rabbit Anti Human Igf Ir, supplied by Boster Bio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio igf 1r rabbit anti rat polyclonal antibody
Fold change of phosphorylation status and total protein content pre‐ to post‐exercise of <t>INSR</t> <t>Tyr1150/1151</t> , Akt Ser473 , AS160 Thr642 , GLUT4, AMPK Thr172 , ACC Ser79 , PDK4, PDH Ser293 and HSL Ser660 ( B ) with representative blots ( A ). Data shown as the mean ± SD. Differences between FAST vs . CARB and CARB vs . NIACIN assessed using a paired t test ( n = 8 males).
Igf 1r Rabbit Anti Rat Polyclonal Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


FIGURE 2. Modulation of IGF/IGF-IR signaling caused by knockdown of IGFBP-2. The IGFBP-2-knockdown cells (IGFBP-2 KD) and control cells were treated with the indicated concentrations of IGF-I or IGF-II in serum-free con- dition, and extents of phosphorylation of IGF-IR (p-IGF-IR), Akt (p-Akt), and ERK1/2 (p-Erk1/2) were analyzed by immunoblot and a representative result of U251 was shown. The band intensity was measured and the ratio of phos- phorylated protein to the corresponding total protein was calculated.

Journal: Journal of Biological Chemistry

Article Title: Silencing of Insulin-like Growth Factor-binding Protein-2 in Human Glioblastoma Cells Reduces Both Invasiveness and Expression of Progression-associated Gene CD24

doi: 10.1074/jbc.m609567200

Figure Lengend Snippet: FIGURE 2. Modulation of IGF/IGF-IR signaling caused by knockdown of IGFBP-2. The IGFBP-2-knockdown cells (IGFBP-2 KD) and control cells were treated with the indicated concentrations of IGF-I or IGF-II in serum-free con- dition, and extents of phosphorylation of IGF-IR (p-IGF-IR), Akt (p-Akt), and ERK1/2 (p-Erk1/2) were analyzed by immunoblot and a representative result of U251 was shown. The band intensity was measured and the ratio of phos- phorylated protein to the corresponding total protein was calculated.

Article Snippet: The following primary antibodies were used: anti-human IGFBP-2 mouse monoclonal antibody (C-10; Santa Cruz Biotechnology, Santa Cruz, CA), anti- -actinmousemonoclonal antibody (AC-74; Sigma), anti-phosphoERK1/2 rabbit monoclonal antibody (Thr185/Tyr187, clone AW39;Upstate Cell Signaling Solutions, Lake Placid, NY), antiphospho-IGF-IR rabbit polyclonal antibody (Tyr1131), antiIGF-IR rabbit polyclonal antibody, anti-phospho-Akt mouse monoclonal antibody (Ser473), anti-Akt rabbit polyclonal antibody, anti-phospho-ERK1/2 rabbit monoclonal antibody (Thr185/Tyr187, clone AW39; Upstate Cell Signaling Solutions, Lake Placid, NY), anti-ERK1/2 rabbit polyclonal antibody, anticaspase-3, and cleaved capase-3 (Asp175) rabbit polyclonal antibodies, and anti-heat shock protein 70 rabbit polyclonal antibody (Cell Signaling Technology, Danvers, MA).

Techniques: Knockdown, Control, Phospho-proteomics, Western Blot

Fold change of phosphorylation status and total protein content pre‐ to post‐exercise of INSR Tyr1150/1151 , Akt Ser473 , AS160 Thr642 , GLUT4, AMPK Thr172 , ACC Ser79 , PDK4, PDH Ser293 and HSL Ser660 ( B ) with representative blots ( A ). Data shown as the mean ± SD. Differences between FAST vs . CARB and CARB vs . NIACIN assessed using a paired t test ( n = 8 males).

Journal: The Journal of Physiology

Article Title: Isolating the effects of carbohydrate and lipid availability on exercise‐induced skeletal muscle signalling in males

doi: 10.1113/JP289864

Figure Lengend Snippet: Fold change of phosphorylation status and total protein content pre‐ to post‐exercise of INSR Tyr1150/1151 , Akt Ser473 , AS160 Thr642 , GLUT4, AMPK Thr172 , ACC Ser79 , PDK4, PDH Ser293 and HSL Ser660 ( B ) with representative blots ( A ). Data shown as the mean ± SD. Differences between FAST vs . CARB and CARB vs . NIACIN assessed using a paired t test ( n = 8 males).

Article Snippet: Membranes were washed again in TBS‐T and incubated in primary antibodies against phospho Ser 79 acetyl‐CoA carboxlyase (ACC) (Cell Signaling Technologies, Danvers, MA, USA), phospho Thr172 AMP‐dependent protein kinase (AMPK) (Cell Signaling Technologies), phospho‐Thr642 Akt substrate of 160 kDa (AS160) (Cell Signaling Technologies), phospho‐Tyr1150/1151 insulin receptor (INS) (Cell Signaling Technologies), phospho‐Ser 473 protein kinase B (Akt) (Cell Signaling Technologie), phospho‐Ser660 hormone‐sensitive lipase (HSL) (Cell Signaling Technologies), phospho‐Ser 293 pyruvate dehydrogenase (PDH) (Cell Signaling Technologies), vinculin (Cell Signaling Technologies), pyruvate dehydrogenase kinase 4 (PDK4) (Abgent, San Diego, CA, USA) and beta‐actin (Protein Technologies, Stockport, UK) overnight at 4°C.

Techniques: Phospho-proteomics