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human fgf 21 quantikine elisa  (R&D Systems)


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    R&D Systems human fgf 21 quantikine elisa
    Human Fgf 21 Quantikine Elisa, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 165 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fgf21/Human+FGF-21+Quantikine+ELISA+Kit/pmc07065370-129-9-7
    Average 95 stars, based on 165 article reviews
    human fgf 21 quantikine elisa - by Bioz Stars, 2026-11
    95/100 stars

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    Related Articles

    Analysis:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Enzyme-linked Immunosorbent Assay:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Clinical Proteomics:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Mouse Assay:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Microscopy:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Sandwich ELISA:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Biomarker Discovery:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Planar Chromatography:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Activity Assay:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to

    Sodium Assay:

    Article Title: Postprandial amino acid profiles and gastric behavior after consumption of milk and plant-based alternatives: a randomized cross-over study in healthy males
    Article Snippet: PrePrint: t, the data were log-transformed before analysis. FGF21: EDTA plasma concentrations were determined using an enzyme-linked immunosorbent assay (ELISA) method (Quantikine® ELISA, catalog number DF2100, R&D Systems) according to the manufacturer’s instructions. The detection range was 31.3 – 2000 pg/ml. 10% of the samples were analyzed in duplo. Coefficients of variation for those ranged from 0.1% to



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    Circulating biomarkers levels in chronic heart failure patients and controls

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Circulating biomarkers levels in chronic heart failure patients and controls

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques:

    Circulating miRNAs and cytokines as molecular signatures of heart failure. Differences in serum levels of GDF-15 and FGF-21 in CHF patients and controls. Serum levels of GDF-15 by ELISA assay in patients with heart failure (HF) ( n = 25) and the control group ( n = 10). ( A ) Data showed significant upregulation of GDF-15 in CHF vs controls ( P < .001). ( B ) FGF-21 levels did not differ significantly between groups. Correlations between GDF-15 and selected miRNAs in CHF patients. ( C , D ) In CHF patients, GDF-15 levels were positively associated with miR-29b ( ρ = 0.42, P = .037) and miR-486 ( ρ = 0.42, P = .039). Data are expressed as fold change and are presented as mean ± SEM. Student's t -test or Mann–Whitney test was used for normally distributed data or non-normally distributed data, respectively. *** P ≤ .001.

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Circulating miRNAs and cytokines as molecular signatures of heart failure. Differences in serum levels of GDF-15 and FGF-21 in CHF patients and controls. Serum levels of GDF-15 by ELISA assay in patients with heart failure (HF) ( n = 25) and the control group ( n = 10). ( A ) Data showed significant upregulation of GDF-15 in CHF vs controls ( P < .001). ( B ) FGF-21 levels did not differ significantly between groups. Correlations between GDF-15 and selected miRNAs in CHF patients. ( C , D ) In CHF patients, GDF-15 levels were positively associated with miR-29b ( ρ = 0.42, P = .037) and miR-486 ( ρ = 0.42, P = .039). Data are expressed as fold change and are presented as mean ± SEM. Student's t -test or Mann–Whitney test was used for normally distributed data or non-normally distributed data, respectively. *** P ≤ .001.

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques: Enzyme-linked Immunosorbent Assay, Control, MANN-WHITNEY

    Molecular profiles in CHF patients. Differences in serum levels of GDF-15 and FGF-21 among heart failure patients with and without cardiac cachexia. Circulating levels of GDF-15 and FGF-21 were analyzed in CHF patients with cardiac cachexia (CC) ( n = 10) and without cardiac cachexia (nCC) ( n = 15), and a control group ( n = 10). ( A ) Significant difference in GDF-15 levels was observed between patients with CC or nCC vs controls (all P < .001). ( B ) Levels of FGF-21 were significantly higher in CHF with CC compared with nCC ( P = .012) and vs controls ( P = .010) ( C ). Spearman’s correlation analysis revealed that in CHF patients with CC, GDF-15 negatively correlated with miR-21 ( ρ = −0.81, P = .007). ( D ) In the same group, FGF-21 negatively correlated with miR-486 ( ρ = −0.69, P = .035). Data are expressed as fold change and are presented as mean ± SEM. One-way ANOVA test or Kruskal–Wallis test was used for normally distributed data or non-normally distributed data, respectively. * P < .05, *** P ≤ .001.

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Molecular profiles in CHF patients. Differences in serum levels of GDF-15 and FGF-21 among heart failure patients with and without cardiac cachexia. Circulating levels of GDF-15 and FGF-21 were analyzed in CHF patients with cardiac cachexia (CC) ( n = 10) and without cardiac cachexia (nCC) ( n = 15), and a control group ( n = 10). ( A ) Significant difference in GDF-15 levels was observed between patients with CC or nCC vs controls (all P < .001). ( B ) Levels of FGF-21 were significantly higher in CHF with CC compared with nCC ( P = .012) and vs controls ( P = .010) ( C ). Spearman’s correlation analysis revealed that in CHF patients with CC, GDF-15 negatively correlated with miR-21 ( ρ = −0.81, P = .007). ( D ) In the same group, FGF-21 negatively correlated with miR-486 ( ρ = −0.69, P = .035). Data are expressed as fold change and are presented as mean ± SEM. One-way ANOVA test or Kruskal–Wallis test was used for normally distributed data or non-normally distributed data, respectively. * P < .05, *** P ≤ .001.

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques: Control, Analysis

    Molecular profiles in cachectic patients with severe CHF. FGF-21 concentrations and their associations with NYHA functional class in patients with CHF. ( A ) Data show higher FGF-21 levels in NYHA class III-IV ( n = 13) compared with class I-II ( n = 9) ( P = .050) and the control group ( n = 10) ( P = .050). ( B ) In NYHA class III-IV, FGF-21 positively correlated with miR-15b ( r = 0.68, P = .014). Data are expressed as fold change and are presented as mean ± SEM. One-way ANOVA test or Kruskal–Wallis test was used for normally distributed data or non-normally distributed data, respectively. * P < .05.

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Molecular profiles in cachectic patients with severe CHF. FGF-21 concentrations and their associations with NYHA functional class in patients with CHF. ( A ) Data show higher FGF-21 levels in NYHA class III-IV ( n = 13) compared with class I-II ( n = 9) ( P = .050) and the control group ( n = 10) ( P = .050). ( B ) In NYHA class III-IV, FGF-21 positively correlated with miR-15b ( r = 0.68, P = .014). Data are expressed as fold change and are presented as mean ± SEM. One-way ANOVA test or Kruskal–Wallis test was used for normally distributed data or non-normally distributed data, respectively. * P < .05.

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques: Functional Assay, Control

    Schematic representation of the circulating molecular profile associated with chronic heart failure and cardiac cachexia, characterized by dysregulation of muscle- and remodelling-related miRNAs and increased stress-responsive cytokines. CHF patients showed reduced miR-15b, miR-29b, miR-133a, and miR-486 and increased GDF-15, while cardiac cachexia was further associated with lower miR-29b and higher FGF-21 levels.

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Schematic representation of the circulating molecular profile associated with chronic heart failure and cardiac cachexia, characterized by dysregulation of muscle- and remodelling-related miRNAs and increased stress-responsive cytokines. CHF patients showed reduced miR-15b, miR-29b, miR-133a, and miR-486 and increased GDF-15, while cardiac cachexia was further associated with lower miR-29b and higher FGF-21 levels.

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques: