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quantikine elisa kits  (R&D Systems)


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    Structured Review

    R&D Systems quantikine elisa kits
    Quantikine Elisa Kits, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 287 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+gdf+15/Human+GDF-15+Quantikine+ELISA+Kit/pmc13624431-104-6-9
    Average 96 stars, based on 287 article reviews
    quantikine elisa kits - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Convergent Roles of Growth Differentiation Factor-15 (GDF-15) in Mechanotransduction, Vascular Disorganization, and Immune Suppression in Melanoma
    Article Snippet: .. 24 h later, conditioned media were collected from the plates and analyzed by GDF-15 ELISA for quantification of protein levels in cell culture media and serum samples, using the DOST ELISA for human GDF-15 (R&D Systems) according to the manufacturer’s protocol. ..

    Article Title: Lower circulating mitochondrial DNA and increased mitokines suggest significant mitochondrial dysfunction in systemic lupus erythematosus with renal involvement.
    Article Snippet: .. GDF- 15 and FGF- 21 levels were assessed in 147 serum and 46 plasma samples by ELISA using the Human GDF- 15 and FGF- 21 ELISA Kit (R&D Systems, Minneapolis, USA). ..

    Article Title: Lower circulating mitochondrial DNA and increased mitokines suggest significant mitochondrial dysfunction in systemic lupus erythematosus with renal involvement
    Article Snippet: .. GDF-15 and FGF-21 levels were assessed in 147 serum and 46 plasma samples by ELISA using the Human GDF-15 and FGF-21 ELISA Kit (R&D Systems, Minneapolis, USA). ..

    Cell Culture:

    Article Title: Convergent Roles of Growth Differentiation Factor-15 (GDF-15) in Mechanotransduction, Vascular Disorganization, and Immune Suppression in Melanoma
    Article Snippet: .. 24 h later, conditioned media were collected from the plates and analyzed by GDF-15 ELISA for quantification of protein levels in cell culture media and serum samples, using the DOST ELISA for human GDF-15 (R&D Systems) according to the manufacturer’s protocol. ..

    Clinical Proteomics:

    Article Title: Lower circulating mitochondrial DNA and increased mitokines suggest significant mitochondrial dysfunction in systemic lupus erythematosus with renal involvement.
    Article Snippet: .. GDF- 15 and FGF- 21 levels were assessed in 147 serum and 46 plasma samples by ELISA using the Human GDF- 15 and FGF- 21 ELISA Kit (R&D Systems, Minneapolis, USA). ..

    Article Title: Lower circulating mitochondrial DNA and increased mitokines suggest significant mitochondrial dysfunction in systemic lupus erythematosus with renal involvement
    Article Snippet: .. GDF-15 and FGF-21 levels were assessed in 147 serum and 46 plasma samples by ELISA using the Human GDF-15 and FGF-21 ELISA Kit (R&D Systems, Minneapolis, USA). ..

    Recombinant:

    Article Title: A-031 Development of novel ELISAs for total GDF-15 and H-specific GDF-15
    Article Snippet: citation ID: hvae106.031 A-031 Development of novel ELISAs for total GDF-15 and H-specific GDF-15 B. Kalra, H. Parekh, A. S. Patel, S. Mistry, M. Hyvonen, and A. Kumar Ansh Labs, Webster, TX University of Cambridge, Cambridge, United Kingdom BACKGROUND: To develop sensitive and specific ELISAs for the quantitative measurement of total human GDF-15 and H-specific (H202D mutant) GDF-15 in human serum, and other biological fluids.. Growth/differentiation Factor 15 (GDF-15) is a divergent member of the TGF-β superfamily of growth factors.. It is encoded in humans by a gene in chromosome 19.

    Article Title: A-030 Evaluation of the Analytical Performance of Two Reproductive Endocrinology Related Assays on the Atellica CI Analyzer
    Article Snippet: citation ID: hvae106.030 A-030 Evaluation of the Analytical Performance of Two Reproductive Endocrinology Related Assays on the Atellica CI Analyzer M. Quintanilla, R. Aleo, J. Warnock, G. Arrode-Bruses, and H. Leipold Siemens Healthcare Diagnostics Inc., Tarrytown, NY BACKGROUND: The Atellica® CI Analyzer is an automated, highthroughput integrated chemistry and immunoassay analyzer utilizing both Atellica® CH and Atellica® IM Assays.. This study evaluated the analytical performance of the Atellica IM Sex Hormone Binding Globulin (SHBG) and the total Testosterone II (TSTII) Assays on the Atellica CI Analyzer.. METHODS: Precision studies were performed according to CLSI EP05-A3 using native and contrived human serum samples.

    Article Title: Senescence of endothelial cells promotes phenotypic changes in adventitial fibroblasts: possible implications for vascular aging
    Article Snippet: .. In addition, hAdv cells were stimulated for 48 h with recombinant human GDF-15 (rhGDF-15; R&D Systems, #957-GD) at concentration of 200 ng/ml. .. In some experiments, hAdv cells were stimulated for 48 h with rhGDF-15 and then erastin (MedChem Express) was added for the next 24 h.

    Concentration Assay:

    Article Title: Senescence of endothelial cells promotes phenotypic changes in adventitial fibroblasts: possible implications for vascular aging
    Article Snippet: .. In addition, hAdv cells were stimulated for 48 h with recombinant human GDF-15 (rhGDF-15; R&D Systems, #957-GD) at concentration of 200 ng/ml. .. In some experiments, hAdv cells were stimulated for 48 h with rhGDF-15 and then erastin (MedChem Express) was added for the next 24 h.



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    Image Search Results


    (A) Proteome Profiler Human XL cytokine array (105 cytokines) of conditioned medium from proliferating, doxorubicin-induced (Dox), and Gem/Cis-induced senescent-like RBE cells. (B) Gdf15 mRNA in proliferating versus senescent-like murine CCA (SB1) cells. (C) Gdf15 mRNA in control vs AP-treated SB-p16-ATTAC tumors. (D) Schematic of in vitro studies. (E-F) Arg1 and iNOS mRNA in bone-marrow-derived macrophage (BMDM) incubated for 72 h with conditioned medium from vehicle- or alisertib-treated SB1 cells expressing shCtrl or shGdf15 . (G) Bulk RNA-seq heatmap (row Z-scores) of naïve bone marrow-derived macrophages (BMDM) cultured 72 h with conditioned media (CM) from SB-p16-shCtrl or SB- p16-Gdf15 OE cells. (H) ARG1 mRNA in human monocyte-derived macrophages ± recombinant human GDF-15 (Qkine Qk017; TGF-β1-free), qRT-PCR relative to vehicle; mean ± SEM, n = 6. (I) Division index (CFSE dilution, normalized to T-cells-only) of anti-CD3/CD28-activated CD8⁺ T cells co-cultured with BMDMs incubated for 72 h with conditioned medium from vehicle- or alisertib-treated SB1 cells expressing shCtrl or shGdf15 . Data are mean ± SEM; *, P<0.05; **, P<0.01; ****, P<0.0001; ns, not significant.

    Journal: bioRxiv

    Article Title: Therapy-induced senescent-like cancer cells drive macrophage-mediated immunosuppression in cholangiocarcinoma

    doi: 10.64898/2026.06.24.734341

    Figure Lengend Snippet: (A) Proteome Profiler Human XL cytokine array (105 cytokines) of conditioned medium from proliferating, doxorubicin-induced (Dox), and Gem/Cis-induced senescent-like RBE cells. (B) Gdf15 mRNA in proliferating versus senescent-like murine CCA (SB1) cells. (C) Gdf15 mRNA in control vs AP-treated SB-p16-ATTAC tumors. (D) Schematic of in vitro studies. (E-F) Arg1 and iNOS mRNA in bone-marrow-derived macrophage (BMDM) incubated for 72 h with conditioned medium from vehicle- or alisertib-treated SB1 cells expressing shCtrl or shGdf15 . (G) Bulk RNA-seq heatmap (row Z-scores) of naïve bone marrow-derived macrophages (BMDM) cultured 72 h with conditioned media (CM) from SB-p16-shCtrl or SB- p16-Gdf15 OE cells. (H) ARG1 mRNA in human monocyte-derived macrophages ± recombinant human GDF-15 (Qkine Qk017; TGF-β1-free), qRT-PCR relative to vehicle; mean ± SEM, n = 6. (I) Division index (CFSE dilution, normalized to T-cells-only) of anti-CD3/CD28-activated CD8⁺ T cells co-cultured with BMDMs incubated for 72 h with conditioned medium from vehicle- or alisertib-treated SB1 cells expressing shCtrl or shGdf15 . Data are mean ± SEM; *, P<0.05; **, P<0.01; ****, P<0.0001; ns, not significant.

    Article Snippet: Human recombinant GDF-15 was from Qkine (Qk017) and murine recombinant GDF-15 from R&D Systems (8944-GD/CF).

    Techniques: Control, In Vitro, Derivative Assay, Incubation, Expressing, RNA Sequencing, Cell Culture, Recombinant, Quantitative RT-PCR

    (A) Macrophages express TGFBR2, the candidate non-canonical GDF-15 receptor, in murine and human CCA single-cell RNA-seq. (B) α-TGFBR2 western blot (WB) of streptavidin pull-down (top) and input (middle) from naïve BMDMs treated with biotin-supplemented conditioned media (CM) from CCA cells expressing GDF-15-BioID2-HA or SEC61B-BioID2-HA (ER control); α-HA blot of CM (bottom) confirms bait secretion. (C) GDF-15 induces macrophage phospho-STAT6 but not phospho-SMAD2/3, reflecting non-canonical TGFBR2 output. (D) WB of BMDMs stimulated with control or GDF-15-overexpressing (GDF-15 OE ) CM for 0 or 1 h: p-STAT6, STAT6, p-SMAD3, SMAD3. (E) Arg1 mRNA in BMDMs transfected with siCtrl or siTgfbr2 and stimulated with control or rGDF-15. n = 6. Data are mean ± SEM; *, P<0.05; **, P<0.01; ****, P<0.0001; ns, not significant.

    Journal: bioRxiv

    Article Title: Therapy-induced senescent-like cancer cells drive macrophage-mediated immunosuppression in cholangiocarcinoma

    doi: 10.64898/2026.06.24.734341

    Figure Lengend Snippet: (A) Macrophages express TGFBR2, the candidate non-canonical GDF-15 receptor, in murine and human CCA single-cell RNA-seq. (B) α-TGFBR2 western blot (WB) of streptavidin pull-down (top) and input (middle) from naïve BMDMs treated with biotin-supplemented conditioned media (CM) from CCA cells expressing GDF-15-BioID2-HA or SEC61B-BioID2-HA (ER control); α-HA blot of CM (bottom) confirms bait secretion. (C) GDF-15 induces macrophage phospho-STAT6 but not phospho-SMAD2/3, reflecting non-canonical TGFBR2 output. (D) WB of BMDMs stimulated with control or GDF-15-overexpressing (GDF-15 OE ) CM for 0 or 1 h: p-STAT6, STAT6, p-SMAD3, SMAD3. (E) Arg1 mRNA in BMDMs transfected with siCtrl or siTgfbr2 and stimulated with control or rGDF-15. n = 6. Data are mean ± SEM; *, P<0.05; **, P<0.01; ****, P<0.0001; ns, not significant.

    Article Snippet: Human recombinant GDF-15 was from Qkine (Qk017) and murine recombinant GDF-15 from R&D Systems (8944-GD/CF).

    Techniques: Single Cell, RNA Sequencing, Western Blot, Expressing, Control, Transfection

    (A) Strategy for p16-promoter-restricted Gdf15 silencing (shRNA) and Gdf15 overexpression. (B) qPCR validation of Gdf15 knockdown and overexpression in senescent-like SB1 cells. (C-D) Subcutaneous model and tumor-burden quantification. (E) GeoMx spatial profiling of GDF-15 expression and macrophage infiltration in human CCA. Region-of-interest (ROI)-level analysis plotting GDF-15 expression against macrophage score; each point is one ROI, with the linear fit and 95% confidence band shown. Spearman ρ = 0.63, P = 0.0067. Data are mean ± SEM; **, P<0.01; ****, P<0.0001.

    Journal: bioRxiv

    Article Title: Therapy-induced senescent-like cancer cells drive macrophage-mediated immunosuppression in cholangiocarcinoma

    doi: 10.64898/2026.06.24.734341

    Figure Lengend Snippet: (A) Strategy for p16-promoter-restricted Gdf15 silencing (shRNA) and Gdf15 overexpression. (B) qPCR validation of Gdf15 knockdown and overexpression in senescent-like SB1 cells. (C-D) Subcutaneous model and tumor-burden quantification. (E) GeoMx spatial profiling of GDF-15 expression and macrophage infiltration in human CCA. Region-of-interest (ROI)-level analysis plotting GDF-15 expression against macrophage score; each point is one ROI, with the linear fit and 95% confidence band shown. Spearman ρ = 0.63, P = 0.0067. Data are mean ± SEM; **, P<0.01; ****, P<0.0001.

    Article Snippet: Human recombinant GDF-15 was from Qkine (Qk017) and murine recombinant GDF-15 from R&D Systems (8944-GD/CF).

    Techniques: shRNA, Over Expression, Biomarker Discovery, Knockdown, Expressing

    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. Circulating miRNA levels and GDF-15 correlations according to ejection fraction and cachexia status in CHF patients. Circulating miRNA levels were analyzed in CHF patients with preserved ejection fraction without cachexia (HFpEF + nCC) ( n = 7) and with reduced ejection fraction with cachexia (HFrEF + CC) ( n = 5) and a control group ( n = 10). ( A ) Data shows significant downregulation of miR-29b ( P = .019) in HFrEF + CC vs HFpEF + nCC and vs controls ( P = .002). ( B ) In HFpEF + nCC, GDF-15 showed a strong positive correlation with miR-29b ( r = 0.82, P = .034). 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 ≤ .01.

    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. Circulating miRNA levels and GDF-15 correlations according to ejection fraction and cachexia status in CHF patients. Circulating miRNA levels were analyzed in CHF patients with preserved ejection fraction without cachexia (HFpEF + nCC) ( n = 7) and with reduced ejection fraction with cachexia (HFrEF + CC) ( n = 5) and a control group ( n = 10). ( A ) Data shows significant downregulation of miR-29b ( P = .019) in HFrEF + CC vs HFpEF + nCC and vs controls ( P = .002). ( B ) In HFpEF + nCC, GDF-15 showed a strong positive correlation with miR-29b ( r = 0.82, P = .034). 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 ≤ .01.

    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

    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:

    Factors associated with GDF-15. Univariate analysis of the correlations of GDF-15 with the (a) estimated glomerular filtration rate (eGFR), (b) ln urine protein-to-creatinine ratio (UPCR), (c) ln N-terminal pro-B-type natriuretic peptide (NT-proBNP), (d) hemoglobin, (e) ln interleukin-6 (IL-6), (f) ln tumor necrosis factor-α (TNF-α), (g) albumin, and (h) lean tissue index.

    Journal: The Journal of Nutrition, Health & Aging

    Article Title: Association of growth differentiation factor-15 with muscle wasting and anemia in chronic kidney disease

    doi: 10.1016/j.jnha.2026.100835

    Figure Lengend Snippet: Factors associated with GDF-15. Univariate analysis of the correlations of GDF-15 with the (a) estimated glomerular filtration rate (eGFR), (b) ln urine protein-to-creatinine ratio (UPCR), (c) ln N-terminal pro-B-type natriuretic peptide (NT-proBNP), (d) hemoglobin, (e) ln interleukin-6 (IL-6), (f) ln tumor necrosis factor-α (TNF-α), (g) albumin, and (h) lean tissue index.

    Article Snippet: Plasma levels of GDF-15 were quantified using the Human GDF-15 Quantikine enzyme-linked immunosorbent assay (ELISA) Kit (R&D Systems, Minneapolis, MN, USA), with intra- and inter-assay coefficients of variation <5%.

    Techniques: Filtration

    Kaplan–Meier curves by growth differentiation factor-15 (GDF-15) median. Participants with GDF-15 concentrations above the median had a higher cumulative incidence of all-cause mortality than those with lower concentrations (log-rank P < 0.001). Numbers at risk are shown below the plot.

    Journal: The Journal of Nutrition, Health & Aging

    Article Title: Association of growth differentiation factor-15 with muscle wasting and anemia in chronic kidney disease

    doi: 10.1016/j.jnha.2026.100835

    Figure Lengend Snippet: Kaplan–Meier curves by growth differentiation factor-15 (GDF-15) median. Participants with GDF-15 concentrations above the median had a higher cumulative incidence of all-cause mortality than those with lower concentrations (log-rank P < 0.001). Numbers at risk are shown below the plot.

    Article Snippet: Plasma levels of GDF-15 were quantified using the Human GDF-15 Quantikine enzyme-linked immunosorbent assay (ELISA) Kit (R&D Systems, Minneapolis, MN, USA), with intra- and inter-assay coefficients of variation <5%.

    Techniques: