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plasma fgf21 concentrations  (R&D Systems)


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    R&D Systems plasma fgf21 concentrations
    Plasma Fgf21 Concentrations, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 218 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/plasma+fgf21/Human+FGF-21+Quantikine+ELISA+Kit/us11372004-352-0-18
    Average 95 stars, based on 218 article reviews
    plasma fgf21 concentrations - by Bioz Stars, 2026-11
    95/100 stars

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    Enzyme-linked Immunosorbent Assay:

    Article Title: Metformin increases glycolysis and the stress-induced cytokine GDF15 but not FGF21 in humans
    Article Snippet: .. Media stored at -80 °C was thawed on ice, and GDF15 and FGF21 protein levels were measured using the Human GDF-15 Quantikine ELISA Kit (R&D Systems, MN, US) and Human FGF-21 Quantikine ELISA Kit (R&D Systems, MN, US) according to the manufacturer’s protocol. .. The optical density was measured on a Spectramax Plus 384 Microplate Reader (Molecular Devices, CA, USA) at wavelengths of 450 nm and 570 nm.

    Article Title: Charting the circulating proteome in ME/CFS using cross-system profiling to uncover mechanistic insights.
    Article Snippet: .. Serum samples were stored at − 80 ◦ C. REAGENT or RESOURCE SOURCE IDENTIFIER Critical commerical assays Custom Luminex Human Discovery assay R&D Systems Cat# LXSAHM; RRID:AB_2924693 Quantikine Ready-To-Use ELISA kit (FGF-21) R&D Systems Cat# DF2100; RRID:AB_2783729 Quantikine Ready-To-Use ELISA kit (GDF-15) R&D Systems Cat# DGD150; RRID:AB_2877710 Quantikine Ready-To-Use ELISA kit (C-peptide) R&D Systems Cat# DICP00 SomaScan Discovery, 7 K SomaLogic Inc v. 4.1 Biological samples Human serum samples ME/CFS Biobank, Haukeland University Hospital, Norway RituxME: NCT02229942 CycloME: NCT02444091 Deposited data Proteomics dataset Deposited in the PRIDE 90 repository (PRIDE: PAD000026) N/A Metabolomics data Hoel et al. 17 ; DOI: https://doi.org/ 10.1172/jci.insight.149217 N/A Software and algorithms GraphPad Prism 9 GraphPad Software N/A R (4.5.1) https://www.r-project.org N/A Rstudio (2025.09.1 + 401) Posit Software N/A R package: Vegan (2.7.0) DOI: https://doi.org/10.32614/CRAN.package.vegan N/A R package: limma (3.64.3) DOI: https://doi.org/10.18129/B9.bioc.limma N/A R package: variancePartition (1.38.1) DOI: https://doi.org/10.18129/B9.bioc.variancePartition N/A R package: ppcor (1.1) DOI: https://doi.org/10.32614/CRAN.package.ppcor N/A R package: clusterProfiler (4.16.0) DOI: https://doi.org/10.18129/B9.bioc.clusterProfiler N/A R package: ComplexHeatmap (2.24.1) DOI: https://doi.org/10.18129/B9.bioc.ComplexHeatmap N/A R package: ggplot2 (4.0.0) DOI: https://doi.org/10.32614/CRAN.package.ggplot2 N/A R package: tidygraph (1.3.1) DOI: https://doi.org/10.32614/CRAN.package.tidygraph N/A R package: igraph (2.2.0) DOI: https://doi.org/10.32614/CRAN.package.igraph N/A R package: ggpubr (0.6.2) DOI: https://doi.org/10.32614/CRAN.package.ggpubr N/A Cellinker DOI: https://doi.org/10.1093/bioinformatics/btab036 N/A BioRender BioRender N/A Microsoft Office Excel Microsoft N/A Other Human protein atlas (HPA) https://www.proteinatlas.org/ N/A Cell Reports Medicine 7, 102647, March 17, 2026 e1 OPEN ACCESS In total, 54 ME/CFS and 29 HC participants were analyzed on the aptamer-platform. ..

    Article Title: Metformin increases glycolysis and the stress-induced cytokine GDF15 but not FGF21 in humans
    Article Snippet: .. FGF21 was measured on fasting serum samples by the human FGF21 Quantikine ® ELISA assay essentially as described (R&D Systems, Abingdon, UK). ..

    Article Title: Charting the circulating proteome in ME/CFS using cross-system profiling to uncover mechanistic insights.
    Article Snippet: .. ELISA was performed using Quantikine Ready-to-Use ELISA kits (R&D Systems) for FGF-21 (Cat#: DF2100), C-peptide (Cat#: DICP00), and GDF-15 (Cat#: DG0150). ..

    Article Title: Charting the circulating proteome in ME/CFS using cross-system profiling to uncover mechanistic insights
    Article Snippet: Seventy-seven target proteins ( ) were quantified using the Luminex Human Discovery Assay (Cat. #LXSAHM; R&D Systems), following the manufacturer’s instructions. .. ELISA was performed using Quantikine Ready-to-Use ELISA kits (R&D Systems) for FGF-21 (Cat#: DF2100), C-peptide (Cat#: DICP00), and GDF-15 (Cat#: DG0150). ..

    Luminex:

    Article Title: Charting the circulating proteome in ME/CFS using cross-system profiling to uncover mechanistic insights.
    Article Snippet: .. Serum samples were stored at − 80 ◦ C. REAGENT or RESOURCE SOURCE IDENTIFIER Critical commerical assays Custom Luminex Human Discovery assay R&D Systems Cat# LXSAHM; RRID:AB_2924693 Quantikine Ready-To-Use ELISA kit (FGF-21) R&D Systems Cat# DF2100; RRID:AB_2783729 Quantikine Ready-To-Use ELISA kit (GDF-15) R&D Systems Cat# DGD150; RRID:AB_2877710 Quantikine Ready-To-Use ELISA kit (C-peptide) R&D Systems Cat# DICP00 SomaScan Discovery, 7 K SomaLogic Inc v. 4.1 Biological samples Human serum samples ME/CFS Biobank, Haukeland University Hospital, Norway RituxME: NCT02229942 CycloME: NCT02444091 Deposited data Proteomics dataset Deposited in the PRIDE 90 repository (PRIDE: PAD000026) N/A Metabolomics data Hoel et al. 17 ; DOI: https://doi.org/ 10.1172/jci.insight.149217 N/A Software and algorithms GraphPad Prism 9 GraphPad Software N/A R (4.5.1) https://www.r-project.org N/A Rstudio (2025.09.1 + 401) Posit Software N/A R package: Vegan (2.7.0) DOI: https://doi.org/10.32614/CRAN.package.vegan N/A R package: limma (3.64.3) DOI: https://doi.org/10.18129/B9.bioc.limma N/A R package: variancePartition (1.38.1) DOI: https://doi.org/10.18129/B9.bioc.variancePartition N/A R package: ppcor (1.1) DOI: https://doi.org/10.32614/CRAN.package.ppcor N/A R package: clusterProfiler (4.16.0) DOI: https://doi.org/10.18129/B9.bioc.clusterProfiler N/A R package: ComplexHeatmap (2.24.1) DOI: https://doi.org/10.18129/B9.bioc.ComplexHeatmap N/A R package: ggplot2 (4.0.0) DOI: https://doi.org/10.32614/CRAN.package.ggplot2 N/A R package: tidygraph (1.3.1) DOI: https://doi.org/10.32614/CRAN.package.tidygraph N/A R package: igraph (2.2.0) DOI: https://doi.org/10.32614/CRAN.package.igraph N/A R package: ggpubr (0.6.2) DOI: https://doi.org/10.32614/CRAN.package.ggpubr N/A Cellinker DOI: https://doi.org/10.1093/bioinformatics/btab036 N/A BioRender BioRender N/A Microsoft Office Excel Microsoft N/A Other Human protein atlas (HPA) https://www.proteinatlas.org/ N/A Cell Reports Medicine 7, 102647, March 17, 2026 e1 OPEN ACCESS In total, 54 ME/CFS and 29 HC participants were analyzed on the aptamer-platform. ..

    Software:

    Article Title: Charting the circulating proteome in ME/CFS using cross-system profiling to uncover mechanistic insights.
    Article Snippet: .. Serum samples were stored at − 80 ◦ C. REAGENT or RESOURCE SOURCE IDENTIFIER Critical commerical assays Custom Luminex Human Discovery assay R&D Systems Cat# LXSAHM; RRID:AB_2924693 Quantikine Ready-To-Use ELISA kit (FGF-21) R&D Systems Cat# DF2100; RRID:AB_2783729 Quantikine Ready-To-Use ELISA kit (GDF-15) R&D Systems Cat# DGD150; RRID:AB_2877710 Quantikine Ready-To-Use ELISA kit (C-peptide) R&D Systems Cat# DICP00 SomaScan Discovery, 7 K SomaLogic Inc v. 4.1 Biological samples Human serum samples ME/CFS Biobank, Haukeland University Hospital, Norway RituxME: NCT02229942 CycloME: NCT02444091 Deposited data Proteomics dataset Deposited in the PRIDE 90 repository (PRIDE: PAD000026) N/A Metabolomics data Hoel et al. 17 ; DOI: https://doi.org/ 10.1172/jci.insight.149217 N/A Software and algorithms GraphPad Prism 9 GraphPad Software N/A R (4.5.1) https://www.r-project.org N/A Rstudio (2025.09.1 + 401) Posit Software N/A R package: Vegan (2.7.0) DOI: https://doi.org/10.32614/CRAN.package.vegan N/A R package: limma (3.64.3) DOI: https://doi.org/10.18129/B9.bioc.limma N/A R package: variancePartition (1.38.1) DOI: https://doi.org/10.18129/B9.bioc.variancePartition N/A R package: ppcor (1.1) DOI: https://doi.org/10.32614/CRAN.package.ppcor N/A R package: clusterProfiler (4.16.0) DOI: https://doi.org/10.18129/B9.bioc.clusterProfiler N/A R package: ComplexHeatmap (2.24.1) DOI: https://doi.org/10.18129/B9.bioc.ComplexHeatmap N/A R package: ggplot2 (4.0.0) DOI: https://doi.org/10.32614/CRAN.package.ggplot2 N/A R package: tidygraph (1.3.1) DOI: https://doi.org/10.32614/CRAN.package.tidygraph N/A R package: igraph (2.2.0) DOI: https://doi.org/10.32614/CRAN.package.igraph N/A R package: ggpubr (0.6.2) DOI: https://doi.org/10.32614/CRAN.package.ggpubr N/A Cellinker DOI: https://doi.org/10.1093/bioinformatics/btab036 N/A BioRender BioRender N/A Microsoft Office Excel Microsoft N/A Other Human protein atlas (HPA) https://www.proteinatlas.org/ N/A Cell Reports Medicine 7, 102647, March 17, 2026 e1 OPEN ACCESS In total, 54 ME/CFS and 29 HC participants were analyzed on the aptamer-platform. ..

    other:

    Article Title: Association of serum fibroblast growth factor 21 levels with coronary artery calcification and coronary intervention in patients with chronic total occlusion
    Article Snippet: Serum FGF21 levels were measured by ELISA (DF2100; R&D Systems, Minneapolis, Minnesota, USA), according to the manufacturer’s instructions.

    Article Title: The Association Between Serum FGF21 Level and Coronary Artery Calcification: Impact of the Degree of Insulin Resistance
    Article Snippet: Serum FGF21 was measured by Enzyme-Linked Immunosorbent Assay (DF2100, R&D Systems, Minneapolis, MN, USA), according to the manufacturer’s instructions.



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    Age and ex-matched SLC25A13 mutation carriers from the TWB were assayed for <t>FGF21</t> circulation and urinary sodium. The data show that male (A) and female (B) mutation carriers have higher levels of FGF21 than control participants and that male and female mutation carriers have higher levels of urinary sodium (C) than control participants. Further, female CD patients have much higher levels of circulating FGF21 than control female age-matched participants (D). (A) Plasma FGF21 levels (N = 25 per group); (B) Plasma FGF21 levels (N = 27 controls, N = 25 carriers); (C) urinary sodium (N = 48 controls, N = 49 carriers); (D) plasma FGF21 (N = 10 controls, N = 2 CD). Symbols: □ male controls; ■ male carriers; ○ female controls; ● female carriers; ● female CD patients. P values are from Student’s t-test.
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    Fig. 3. Effect of FGH21 addition on GH signaling. A, B) Immunoblotting of JAK2, p-JAK2, STAT5b, and HSP90. Fao cells were cultured in the Full or Zero medium with 0–10 [5] pM of recombinant <t>FGF21</t> for 24 h. Cells were then treated with 100 nM GH or vehicle for 10 min. C) Igf1 mRNA levels were quantified using real-time qPCR. Values were normalized against the Actb mRNA level. Fao cells were cultured in the full medium with or without 100 nM GH and 0–105 pM of FGF21 for 24 h. Total RNA was isolated. Bar: means ± SEM (n = 3), *p < 0.05. (D) The expression of α-klotho (Kl), β-klotho (Klb), and FGF Receptor (Fgfr) 1–4 in Fao cells, rat primary hepatocytes, and rat tissue samples were analyzed using reverse transcription-PCR. (E) Immnoblotting of Erk and p-Erk. Fao cells were cultured in the full medium for 24 h. The cells were then treated with 0–104 pM of FGF21 or vehicle for 10 min.
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    R&D Systems plasma fgf21
    Fig. 3. Effect of FGH21 addition on GH signaling. A, B) Immunoblotting of JAK2, p-JAK2, STAT5b, and HSP90. Fao cells were cultured in the Full or Zero medium with 0–10 [5] pM of recombinant <t>FGF21</t> for 24 h. Cells were then treated with 100 nM GH or vehicle for 10 min. C) Igf1 mRNA levels were quantified using real-time qPCR. Values were normalized against the Actb mRNA level. Fao cells were cultured in the full medium with or without 100 nM GH and 0–105 pM of FGF21 for 24 h. Total RNA was isolated. Bar: means ± SEM (n = 3), *p < 0.05. (D) The expression of α-klotho (Kl), β-klotho (Klb), and FGF Receptor (Fgfr) 1–4 in Fao cells, rat primary hepatocytes, and rat tissue samples were analyzed using reverse transcription-PCR. (E) Immnoblotting of Erk and p-Erk. Fao cells were cultured in the full medium for 24 h. The cells were then treated with 0–104 pM of FGF21 or vehicle for 10 min.
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    Age and ex-matched SLC25A13 mutation carriers from the TWB were assayed for FGF21 circulation and urinary sodium. The data show that male (A) and female (B) mutation carriers have higher levels of FGF21 than control participants and that male and female mutation carriers have higher levels of urinary sodium (C) than control participants. Further, female CD patients have much higher levels of circulating FGF21 than control female age-matched participants (D). (A) Plasma FGF21 levels (N = 25 per group); (B) Plasma FGF21 levels (N = 27 controls, N = 25 carriers); (C) urinary sodium (N = 48 controls, N = 49 carriers); (D) plasma FGF21 (N = 10 controls, N = 2 CD). Symbols: □ male controls; ■ male carriers; ○ female controls; ● female carriers; ● female CD patients. P values are from Student’s t-test.

    Journal: medRxiv

    Article Title: Elevated FGF21 and triglycerides in SLC25A13 carriers support the G3P-ChREBP Citrin Deficiency disease hypothesis

    doi: 10.64898/2025.12.10.25342016

    Figure Lengend Snippet: Age and ex-matched SLC25A13 mutation carriers from the TWB were assayed for FGF21 circulation and urinary sodium. The data show that male (A) and female (B) mutation carriers have higher levels of FGF21 than control participants and that male and female mutation carriers have higher levels of urinary sodium (C) than control participants. Further, female CD patients have much higher levels of circulating FGF21 than control female age-matched participants (D). (A) Plasma FGF21 levels (N = 25 per group); (B) Plasma FGF21 levels (N = 27 controls, N = 25 carriers); (C) urinary sodium (N = 48 controls, N = 49 carriers); (D) plasma FGF21 (N = 10 controls, N = 2 CD). Symbols: □ male controls; ■ male carriers; ○ female controls; ● female carriers; ● female CD patients. P values are from Student’s t-test.

    Article Snippet: Plasma FGF21 levels were quantified in duplicate using the Quantikine® Human FGF-21 ELISA kit (R&D Systems, DF2100) according to the manufacturer’s protocol.

    Techniques: Mutagenesis, Control, Clinical Proteomics

    (A) TGs were compared between the N = 7 control participants and the N =45 SLC25A13 mutation carriers for whom TG values were available in the TWB. These data show a nonsignificant TG increase in mutation carriers. (B) A plot of TGs as a function of FGF21 in mutation carriers shows a strong positive correlation (Pearson’s correlation R = 0.58) that is counter to the depression of TGs by genetically proxied FGF21 in the general population and consistent with elevation of FGF21 and lipogenic transcription by a potentiated ChREBP system in SLC25A13 carriers.

    Journal: medRxiv

    Article Title: Elevated FGF21 and triglycerides in SLC25A13 carriers support the G3P-ChREBP Citrin Deficiency disease hypothesis

    doi: 10.64898/2025.12.10.25342016

    Figure Lengend Snippet: (A) TGs were compared between the N = 7 control participants and the N =45 SLC25A13 mutation carriers for whom TG values were available in the TWB. These data show a nonsignificant TG increase in mutation carriers. (B) A plot of TGs as a function of FGF21 in mutation carriers shows a strong positive correlation (Pearson’s correlation R = 0.58) that is counter to the depression of TGs by genetically proxied FGF21 in the general population and consistent with elevation of FGF21 and lipogenic transcription by a potentiated ChREBP system in SLC25A13 carriers.

    Article Snippet: Plasma FGF21 levels were quantified in duplicate using the Quantikine® Human FGF-21 ELISA kit (R&D Systems, DF2100) according to the manufacturer’s protocol.

    Techniques: Control, Mutagenesis

    Fig. 3. Effect of FGH21 addition on GH signaling. A, B) Immunoblotting of JAK2, p-JAK2, STAT5b, and HSP90. Fao cells were cultured in the Full or Zero medium with 0–10 [5] pM of recombinant FGF21 for 24 h. Cells were then treated with 100 nM GH or vehicle for 10 min. C) Igf1 mRNA levels were quantified using real-time qPCR. Values were normalized against the Actb mRNA level. Fao cells were cultured in the full medium with or without 100 nM GH and 0–105 pM of FGF21 for 24 h. Total RNA was isolated. Bar: means ± SEM (n = 3), *p < 0.05. (D) The expression of α-klotho (Kl), β-klotho (Klb), and FGF Receptor (Fgfr) 1–4 in Fao cells, rat primary hepatocytes, and rat tissue samples were analyzed using reverse transcription-PCR. (E) Immnoblotting of Erk and p-Erk. Fao cells were cultured in the full medium for 24 h. The cells were then treated with 0–104 pM of FGF21 or vehicle for 10 min.

    Journal: Biochemical and biophysical research communications

    Article Title: Growth hormone resistance induced by amino acid deprivation in fao cells is independent of FGF21.

    doi: 10.1016/j.bbrc.2024.149811

    Figure Lengend Snippet: Fig. 3. Effect of FGH21 addition on GH signaling. A, B) Immunoblotting of JAK2, p-JAK2, STAT5b, and HSP90. Fao cells were cultured in the Full or Zero medium with 0–10 [5] pM of recombinant FGF21 for 24 h. Cells were then treated with 100 nM GH or vehicle for 10 min. C) Igf1 mRNA levels were quantified using real-time qPCR. Values were normalized against the Actb mRNA level. Fao cells were cultured in the full medium with or without 100 nM GH and 0–105 pM of FGF21 for 24 h. Total RNA was isolated. Bar: means ± SEM (n = 3), *p < 0.05. (D) The expression of α-klotho (Kl), β-klotho (Klb), and FGF Receptor (Fgfr) 1–4 in Fao cells, rat primary hepatocytes, and rat tissue samples were analyzed using reverse transcription-PCR. (E) Immnoblotting of Erk and p-Erk. Fao cells were cultured in the full medium for 24 h. The cells were then treated with 0–104 pM of FGF21 or vehicle for 10 min.

    Article Snippet: Plasma FGF21 concentrations were measured using a mouse/rat FGF21 ELISA kit (Proteintech, IL, USA).

    Techniques: Western Blot, Cell Culture, Recombinant, Isolation, Expressing, Reverse Transcription