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Novus Biologicals
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Image Search Results
Journal: FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Article Title: Elevated chemerin induces insulin resistance in human granulosa-lutein cells from polycystic ovary syndrome patients.
doi: 10.1096/fj.201802829R
Figure Lengend Snippet: Figure 1. Insulin signaling pathway was impaired in hGLs from patients with PCOS with IR. Insulin-stimulated IR-b Tyr1150/1151 phosphorylation (A, B), IRS1 Ser307 phosphorylation (A, C), total IRS2 expression (A, D), IRS1/2 Tyr612 phosphorylation (A, E), Akt Ser473 phosphorylation (A, F), and glucose uptake (A, G) in hGLs from either patients without PCOS without IR (n = 7) or with IR (n = 7) and either patients with PCOS without IR (n = 7) or with IR (n = 7). All values are means 6 SEM. *P , 0.05, **P , 0.01, against insulin in non-PCOS without IR or PCOS with IR group; &P , 0.05, against insulin in non-PCOS with IR group; #P , 0.05, ##P , 0.01, against insulin in PCOS without IR group.
Article Snippet: After determination of protein concentration by Bradford assay, 30 mg of protein from each sample was electrophoresed on a 10% SDS-polyacrylamide gel and transferred to a nitrocellulosemembrane.After blockingwith 5% nonfat milk, the membrane was incubated overnight at 4°C with antibodies against chemerin (1:1000 dilutions, AF2324; R&D Systems), CMKLR1 (1:500 dilutions, ab64881; Abcam), total insulin receptor b subunit (IR-b) (1:1000 dilutions, 3025; Cell Signaling Technology, Danvers, MA, USA), phosphorylated (phosphor)-IR (Tyr1150/1151) (1:1000 dilutions, 3024; Cell Signaling Technology), total IRS1 (1:500 dilutions, ab40777; Abcam),
Techniques: Phospho-proteomics, Expressing
Journal: FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Article Title: Elevated chemerin induces insulin resistance in human granulosa-lutein cells from polycystic ovary syndrome patients.
doi: 10.1096/fj.201802829R
Figure Lengend Snippet: Figure 3. Chemerin impaired insulin signaling and glucose uptake in cultured hGLs. A–E) Effect of prior chemerin (100 ng/ml, 24 h) treatment on the levels of IR-b Tyr1150/1151 phosphorylation (A, B), IRS1 Ser307 phosphorylation (A, C), IRS1/2 Tyr612 phosphorylation (A, D), and Akt Ser473 phosphorylation (A, E) (n = 5) after insulin (100 nM; 15 min) stimulation. F) Effect of prior chemerin (100 ng/ml, 24 h) treatment on total GLUT4 expression (n = 5). G–H) Effect of prior chemerin (100 ng/ml, 24 h) treatment on GLUT4 translocation (membrane GLUT4/cytoplasm GLUT4) (n = 5) and glucose uptake (n = 5) after insulin (100 nM, 30 min) stimulation. All values are means 6 SEM. *P , 0.05, **P , 0.01, ***P , 0.001, against control; #P , 0.05, ##P , 0.01, against +insulin.
Article Snippet: After determination of protein concentration by Bradford assay, 30 mg of protein from each sample was electrophoresed on a 10% SDS-polyacrylamide gel and transferred to a nitrocellulosemembrane.After blockingwith 5% nonfat milk, the membrane was incubated overnight at 4°C with antibodies against chemerin (1:1000 dilutions, AF2324; R&D Systems), CMKLR1 (1:500 dilutions, ab64881; Abcam), total insulin receptor b subunit (IR-b) (1:1000 dilutions, 3025; Cell Signaling Technology, Danvers, MA, USA), phosphorylated (phosphor)-IR (Tyr1150/1151) (1:1000 dilutions, 3024; Cell Signaling Technology), total IRS1 (1:500 dilutions, ab40777; Abcam),
Techniques: Cell Culture, Phospho-proteomics, Expressing, Translocation Assay, Membrane, Control
Journal: FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Article Title: Elevated chemerin induces insulin resistance in human granulosa-lutein cells from polycystic ovary syndrome patients.
doi: 10.1096/fj.201802829R
Figure Lengend Snippet: Figure 4. Knockdown of CMKLR1 restored insulin sensitivity in chemerin-treated hGLs. A) Efficacy of siRNA-mediated knockdown of CMKLR1 in hGLs (n = 4). B–G) Effect of prior chemerin (100 ng/ml, 24 h) treatment on the induction of IRS1 Ser307 phosphorylation (B, C), IRS1/2 Tyr612 phosphorylation (B, D), Akt Ser473 phosphorylation (B, E), GLUT4 translocation (membrane GLUT4/cytoplasm GLUT4) (F) (n = 4), and glucose uptake (G) (n = 4) by insulin (100 nM) in the presence or absence of siRNA-mediated knockdown of CMKLR1. All values are means 6 SEM. *P , 0.05, **P , 0.01, ***P , 0.001, against negative control (NC) or +insulin; #P , 0.05, ##P , 0.01, against chemerin + insulin.
Article Snippet: After determination of protein concentration by Bradford assay, 30 mg of protein from each sample was electrophoresed on a 10% SDS-polyacrylamide gel and transferred to a nitrocellulosemembrane.After blockingwith 5% nonfat milk, the membrane was incubated overnight at 4°C with antibodies against chemerin (1:1000 dilutions, AF2324; R&D Systems), CMKLR1 (1:500 dilutions, ab64881; Abcam), total insulin receptor b subunit (IR-b) (1:1000 dilutions, 3025; Cell Signaling Technology, Danvers, MA, USA), phosphorylated (phosphor)-IR (Tyr1150/1151) (1:1000 dilutions, 3024; Cell Signaling Technology), total IRS1 (1:500 dilutions, ab40777; Abcam),
Techniques: Knockdown, Phospho-proteomics, Translocation Assay, Membrane, Negative Control