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quantikine human gdf15 nag 1 elisa kit  (R&D Systems)
99
R&D Systems quantikine human gdf15 nag 1 elisa kit
Expression levels of <t>NAG-1,</t> and its transcription factor EGR-1, are induced in PC-3 cells upon GLP treatment. (A) Quantification of the mRNA expression levels of NAG-1 and EGR-1 in a time-dependent manner (0-24 h) following treatment of PC-3 cells with 5 mg/ml GLP. Data are presented as the means ± standard error from three independent experiments. Two-way ANOVA with post hoc Bonferroni's correction for multiple comparison was used to determine statistical significance. * indicates time-dependent effects; # indicates effects of GLP treatment. * P<0.05 and ** P<0.01 compared with the 0 h group for each treatment. # P<0.05 and ## P<0.01 compared with the untreated control group at each time-point. (B) Quantification of the mRNA expression levels of NAG-1 and EGR-1 in a dose-dependent manner following treatment of PC-3 cells with GLP (0-10 mg/ml) for 24 h. Induction of EGR-1 and NAG-1 protein expression upon GLP treatment in a (C) time-dependent and (D) dose-dependent manner, as determined by western blotting. β-actin was used as an internal control. (E) GLP induced NAG-1 promoter activity, as determined by luciferase assay. Fold-changes were normalized to pRL-null expressing Renilla luciferase protein. (F) ELISA of the concentration of NAG-1 protein in the cell culture medium following treatment with 0-10 mg/ml GLP for 48 h. Data presented were normalized to the concentration of protein in lysates from each sample. All data are presented as the means ± standard error of three independent experiments. * P<0.05, ** P<0.01 compared with the control group (one-way ANOVA with Dunnett's correction). ANOVA, analysis of variance; EGR-1, early growth response-1; GLP, Ganoderma lucidum polysaccharides; NAG-1, non-steroidal anti-inflammatory drug-activated gene-1; RLU, relative light units.
Quantikine Human Gdf15 Nag 1 Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/quantikine human gdf15 nag 1 elisa kit/product/R&D Systems
Average 99 stars, based on 1 article reviews
quantikine human gdf15 nag 1 elisa kit - by Bioz Stars, 2026-03
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gdf 15 dy957  (R&D Systems)
94
R&D Systems gdf 15 dy957
Expression levels of <t>NAG-1,</t> and its transcription factor EGR-1, are induced in PC-3 cells upon GLP treatment. (A) Quantification of the mRNA expression levels of NAG-1 and EGR-1 in a time-dependent manner (0-24 h) following treatment of PC-3 cells with 5 mg/ml GLP. Data are presented as the means ± standard error from three independent experiments. Two-way ANOVA with post hoc Bonferroni's correction for multiple comparison was used to determine statistical significance. * indicates time-dependent effects; # indicates effects of GLP treatment. * P<0.05 and ** P<0.01 compared with the 0 h group for each treatment. # P<0.05 and ## P<0.01 compared with the untreated control group at each time-point. (B) Quantification of the mRNA expression levels of NAG-1 and EGR-1 in a dose-dependent manner following treatment of PC-3 cells with GLP (0-10 mg/ml) for 24 h. Induction of EGR-1 and NAG-1 protein expression upon GLP treatment in a (C) time-dependent and (D) dose-dependent manner, as determined by western blotting. β-actin was used as an internal control. (E) GLP induced NAG-1 promoter activity, as determined by luciferase assay. Fold-changes were normalized to pRL-null expressing Renilla luciferase protein. (F) ELISA of the concentration of NAG-1 protein in the cell culture medium following treatment with 0-10 mg/ml GLP for 48 h. Data presented were normalized to the concentration of protein in lysates from each sample. All data are presented as the means ± standard error of three independent experiments. * P<0.05, ** P<0.01 compared with the control group (one-way ANOVA with Dunnett's correction). ANOVA, analysis of variance; EGR-1, early growth response-1; GLP, Ganoderma lucidum polysaccharides; NAG-1, non-steroidal anti-inflammatory drug-activated gene-1; RLU, relative light units.
Gdf 15 Dy957, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gdf 15 dy957/product/R&D Systems
Average 94 stars, based on 1 article reviews
gdf 15 dy957 - by Bioz Stars, 2026-03
94/100 stars
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Expression levels of NAG-1, and its transcription factor EGR-1, are induced in PC-3 cells upon GLP treatment. (A) Quantification of the mRNA expression levels of NAG-1 and EGR-1 in a time-dependent manner (0-24 h) following treatment of PC-3 cells with 5 mg/ml GLP. Data are presented as the means ± standard error from three independent experiments. Two-way ANOVA with post hoc Bonferroni's correction for multiple comparison was used to determine statistical significance. * indicates time-dependent effects; # indicates effects of GLP treatment. * P<0.05 and ** P<0.01 compared with the 0 h group for each treatment. # P<0.05 and ## P<0.01 compared with the untreated control group at each time-point. (B) Quantification of the mRNA expression levels of NAG-1 and EGR-1 in a dose-dependent manner following treatment of PC-3 cells with GLP (0-10 mg/ml) for 24 h. Induction of EGR-1 and NAG-1 protein expression upon GLP treatment in a (C) time-dependent and (D) dose-dependent manner, as determined by western blotting. β-actin was used as an internal control. (E) GLP induced NAG-1 promoter activity, as determined by luciferase assay. Fold-changes were normalized to pRL-null expressing Renilla luciferase protein. (F) ELISA of the concentration of NAG-1 protein in the cell culture medium following treatment with 0-10 mg/ml GLP for 48 h. Data presented were normalized to the concentration of protein in lysates from each sample. All data are presented as the means ± standard error of three independent experiments. * P<0.05, ** P<0.01 compared with the control group (one-way ANOVA with Dunnett's correction). ANOVA, analysis of variance; EGR-1, early growth response-1; GLP, Ganoderma lucidum polysaccharides; NAG-1, non-steroidal anti-inflammatory drug-activated gene-1; RLU, relative light units.

Journal: International Journal of Oncology

Article Title: Effects of non-steroidal anti-inflammatory drug-activated gene-1 on Ganoderma lucidum polysaccharides-induced apoptosis of human prostate cancer PC-3 cells

doi: 10.3892/ijo.2018.4578

Figure Lengend Snippet: Expression levels of NAG-1, and its transcription factor EGR-1, are induced in PC-3 cells upon GLP treatment. (A) Quantification of the mRNA expression levels of NAG-1 and EGR-1 in a time-dependent manner (0-24 h) following treatment of PC-3 cells with 5 mg/ml GLP. Data are presented as the means ± standard error from three independent experiments. Two-way ANOVA with post hoc Bonferroni's correction for multiple comparison was used to determine statistical significance. * indicates time-dependent effects; # indicates effects of GLP treatment. * P<0.05 and ** P<0.01 compared with the 0 h group for each treatment. # P<0.05 and ## P<0.01 compared with the untreated control group at each time-point. (B) Quantification of the mRNA expression levels of NAG-1 and EGR-1 in a dose-dependent manner following treatment of PC-3 cells with GLP (0-10 mg/ml) for 24 h. Induction of EGR-1 and NAG-1 protein expression upon GLP treatment in a (C) time-dependent and (D) dose-dependent manner, as determined by western blotting. β-actin was used as an internal control. (E) GLP induced NAG-1 promoter activity, as determined by luciferase assay. Fold-changes were normalized to pRL-null expressing Renilla luciferase protein. (F) ELISA of the concentration of NAG-1 protein in the cell culture medium following treatment with 0-10 mg/ml GLP for 48 h. Data presented were normalized to the concentration of protein in lysates from each sample. All data are presented as the means ± standard error of three independent experiments. * P<0.05, ** P<0.01 compared with the control group (one-way ANOVA with Dunnett's correction). ANOVA, analysis of variance; EGR-1, early growth response-1; GLP, Ganoderma lucidum polysaccharides; NAG-1, non-steroidal anti-inflammatory drug-activated gene-1; RLU, relative light units.

Article Snippet: The Quantikine Human GDF15/NAG-1 ELISA kit (cat. no. DY957) was purchased from R&D Systems, Inc. (Minneapolis, MN, USA).

Techniques: Expressing, Comparison, Western Blot, Activity Assay, Luciferase, Enzyme-linked Immunosorbent Assay, Concentration Assay, Cell Culture

GLP-induced apoptosis of PC-3 cells is mediated through NAG-1 induction. (A) NAG-1 siRNA successfully knocked down NAG-1 expression in PC-3 cells, as determined by western blotting. (B) NAG-1 siRNA inhibited GLP-induced NAG-1 expression, as determined by western blotting. (C) NAG-1 siRNA inhibited GLP-induced apoptosis, as determined by flow cytometry. Percentage of early and late apoptotic of PC-3 cells induced by GLP is presented in the lower panel. (D) NAG-1 siRNA inhibited GLP-induced PARP cleavage and the suppression of pro-caspase-3, -6 and -9 protein expression. β-actin was used as an internal control. Data are presented as the means ± standard error. * P<0.05, ** P<0.01 compared with the control group (one-way analysis of variance with Dunnett's correction). ## P<0.01, compared with GLP-treated cells. GLP, Ganoderma lucidum polysaccharides; NAG-1, non-steroidal anti-inflammatory drug-activated gene-1; PARP, poly(ADP-ribose) polymerase; PI, propidium iodide; siRNA, small interfering RNA.

Journal: International Journal of Oncology

Article Title: Effects of non-steroidal anti-inflammatory drug-activated gene-1 on Ganoderma lucidum polysaccharides-induced apoptosis of human prostate cancer PC-3 cells

doi: 10.3892/ijo.2018.4578

Figure Lengend Snippet: GLP-induced apoptosis of PC-3 cells is mediated through NAG-1 induction. (A) NAG-1 siRNA successfully knocked down NAG-1 expression in PC-3 cells, as determined by western blotting. (B) NAG-1 siRNA inhibited GLP-induced NAG-1 expression, as determined by western blotting. (C) NAG-1 siRNA inhibited GLP-induced apoptosis, as determined by flow cytometry. Percentage of early and late apoptotic of PC-3 cells induced by GLP is presented in the lower panel. (D) NAG-1 siRNA inhibited GLP-induced PARP cleavage and the suppression of pro-caspase-3, -6 and -9 protein expression. β-actin was used as an internal control. Data are presented as the means ± standard error. * P<0.05, ** P<0.01 compared with the control group (one-way analysis of variance with Dunnett's correction). ## P<0.01, compared with GLP-treated cells. GLP, Ganoderma lucidum polysaccharides; NAG-1, non-steroidal anti-inflammatory drug-activated gene-1; PARP, poly(ADP-ribose) polymerase; PI, propidium iodide; siRNA, small interfering RNA.

Article Snippet: The Quantikine Human GDF15/NAG-1 ELISA kit (cat. no. DY957) was purchased from R&D Systems, Inc. (Minneapolis, MN, USA).

Techniques: Expressing, Western Blot, Flow Cytometry, Small Interfering RNA

Working model of the molecular mechanisms by which GLP exerts its anticancer activity in prostate cancer PC-3 cells. GLP-induced apoptosis is mediated by NAG-1 induction, which may serve a pivotal role in GLP-induced cell death in prostate cancer cells.

Journal: International Journal of Oncology

Article Title: Effects of non-steroidal anti-inflammatory drug-activated gene-1 on Ganoderma lucidum polysaccharides-induced apoptosis of human prostate cancer PC-3 cells

doi: 10.3892/ijo.2018.4578

Figure Lengend Snippet: Working model of the molecular mechanisms by which GLP exerts its anticancer activity in prostate cancer PC-3 cells. GLP-induced apoptosis is mediated by NAG-1 induction, which may serve a pivotal role in GLP-induced cell death in prostate cancer cells.

Article Snippet: The Quantikine Human GDF15/NAG-1 ELISA kit (cat. no. DY957) was purchased from R&D Systems, Inc. (Minneapolis, MN, USA).

Techniques: Activity Assay