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mouse rat gdf15 quantikine elisa kit  (R&D Systems)


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    Structured Review

    R&D Systems mouse rat gdf15 quantikine elisa kit
    a, Daily food intake (g per mouse) measured in HFD-fed mice receiving daily intraperitoneal injections of vehicle (VEH) or BAY2402234 (BAY) at ZT0 or ZT12 for 7 consecutive days (n=20/group). b, Distribution of food intake between light and dark phases for the same conditions as in ( a) (n=4 cages/group). c, Representative immunoblots of hepatic FGF21 collected 4 h and 16 h after VEH or BAY injection at ZT0 (top) or ZT12 (bottom). LC, loading control. n=4/group/timepoint. d, Densitometric quantification of FGF21 normalized to LC at 4 h and 16 h after injection; ns, not significant; P < 0.05. e,g, Serum <t>GDF15</t> measured 4 h and 16 h after VEH or BAY injection at ZT0 ( e ; sampling at ZT4 and ZT16) or ZT12 ( g ; sampling at ZT16 and ZT4), respectively. n=4/group/timepoint. f,h, Daily water intake following injections at ZT0 ( f ) or ZT12 ( h ). n=8/group/timepoint. Data are mean ± s.e.m. Statistical comparisons were performed between VEH and BAY at each matched time point; ns, not significant; * P < 0.05. All experiments were performed in male C57BL/6J mice.
    Mouse Rat Gdf15 Quantikine Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 127 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse rat gdf15 quantikine elisa kit/product/R&D Systems
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    mouse rat gdf15 quantikine elisa kit - by Bioz Stars, 2026-05
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    Images

    1) Product Images from "Chronopharmacological targeting of mitochondrial dihydroorotate dehydrogenase prevents diet-induced obesity in male mice"

    Article Title: Chronopharmacological targeting of mitochondrial dihydroorotate dehydrogenase prevents diet-induced obesity in male mice

    Journal: bioRxiv

    doi: 10.64898/2026.04.18.719366

    a, Daily food intake (g per mouse) measured in HFD-fed mice receiving daily intraperitoneal injections of vehicle (VEH) or BAY2402234 (BAY) at ZT0 or ZT12 for 7 consecutive days (n=20/group). b, Distribution of food intake between light and dark phases for the same conditions as in ( a) (n=4 cages/group). c, Representative immunoblots of hepatic FGF21 collected 4 h and 16 h after VEH or BAY injection at ZT0 (top) or ZT12 (bottom). LC, loading control. n=4/group/timepoint. d, Densitometric quantification of FGF21 normalized to LC at 4 h and 16 h after injection; ns, not significant; P < 0.05. e,g, Serum GDF15 measured 4 h and 16 h after VEH or BAY injection at ZT0 ( e ; sampling at ZT4 and ZT16) or ZT12 ( g ; sampling at ZT16 and ZT4), respectively. n=4/group/timepoint. f,h, Daily water intake following injections at ZT0 ( f ) or ZT12 ( h ). n=8/group/timepoint. Data are mean ± s.e.m. Statistical comparisons were performed between VEH and BAY at each matched time point; ns, not significant; * P < 0.05. All experiments were performed in male C57BL/6J mice.
    Figure Legend Snippet: a, Daily food intake (g per mouse) measured in HFD-fed mice receiving daily intraperitoneal injections of vehicle (VEH) or BAY2402234 (BAY) at ZT0 or ZT12 for 7 consecutive days (n=20/group). b, Distribution of food intake between light and dark phases for the same conditions as in ( a) (n=4 cages/group). c, Representative immunoblots of hepatic FGF21 collected 4 h and 16 h after VEH or BAY injection at ZT0 (top) or ZT12 (bottom). LC, loading control. n=4/group/timepoint. d, Densitometric quantification of FGF21 normalized to LC at 4 h and 16 h after injection; ns, not significant; P < 0.05. e,g, Serum GDF15 measured 4 h and 16 h after VEH or BAY injection at ZT0 ( e ; sampling at ZT4 and ZT16) or ZT12 ( g ; sampling at ZT16 and ZT4), respectively. n=4/group/timepoint. f,h, Daily water intake following injections at ZT0 ( f ) or ZT12 ( h ). n=8/group/timepoint. Data are mean ± s.e.m. Statistical comparisons were performed between VEH and BAY at each matched time point; ns, not significant; * P < 0.05. All experiments were performed in male C57BL/6J mice.

    Techniques Used: Western Blot, Injection, Control, Sampling



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    a, Daily food intake (g per mouse) measured in HFD-fed mice receiving daily intraperitoneal injections of vehicle (VEH) or BAY2402234 (BAY) at ZT0 or ZT12 for 7 consecutive days (n=20/group). b, Distribution of food intake between light and dark phases for the same conditions as in ( a) (n=4 cages/group). c, Representative immunoblots of hepatic FGF21 collected 4 h and 16 h after VEH or BAY injection at ZT0 (top) or ZT12 (bottom). LC, loading control. n=4/group/timepoint. d, Densitometric quantification of FGF21 normalized to LC at 4 h and 16 h after injection; ns, not significant; P < 0.05. e,g, Serum <t>GDF15</t> measured 4 h and 16 h after VEH or BAY injection at ZT0 ( e ; sampling at ZT4 and ZT16) or ZT12 ( g ; sampling at ZT16 and ZT4), respectively. n=4/group/timepoint. f,h, Daily water intake following injections at ZT0 ( f ) or ZT12 ( h ). n=8/group/timepoint. Data are mean ± s.e.m. Statistical comparisons were performed between VEH and BAY at each matched time point; ns, not significant; * P < 0.05. All experiments were performed in male C57BL/6J mice.
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    a, Daily food intake (g per mouse) measured in HFD-fed mice receiving daily intraperitoneal injections of vehicle (VEH) or BAY2402234 (BAY) at ZT0 or ZT12 for 7 consecutive days (n=20/group). b, Distribution of food intake between light and dark phases for the same conditions as in ( a) (n=4 cages/group). c, Representative immunoblots of hepatic FGF21 collected 4 h and 16 h after VEH or BAY injection at ZT0 (top) or ZT12 (bottom). LC, loading control. n=4/group/timepoint. d, Densitometric quantification of FGF21 normalized to LC at 4 h and 16 h after injection; ns, not significant; P < 0.05. e,g, Serum <t>GDF15</t> measured 4 h and 16 h after VEH or BAY injection at ZT0 ( e ; sampling at ZT4 and ZT16) or ZT12 ( g ; sampling at ZT16 and ZT4), respectively. n=4/group/timepoint. f,h, Daily water intake following injections at ZT0 ( f ) or ZT12 ( h ). n=8/group/timepoint. Data are mean ± s.e.m. Statistical comparisons were performed between VEH and BAY at each matched time point; ns, not significant; * P < 0.05. All experiments were performed in male C57BL/6J mice.
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    a, Daily food intake (g per mouse) measured in HFD-fed mice receiving daily intraperitoneal injections of vehicle (VEH) or BAY2402234 (BAY) at ZT0 or ZT12 for 7 consecutive days (n=20/group). b, Distribution of food intake between light and dark phases for the same conditions as in ( a) (n=4 cages/group). c, Representative immunoblots of hepatic FGF21 collected 4 h and 16 h after VEH or BAY injection at ZT0 (top) or ZT12 (bottom). LC, loading control. n=4/group/timepoint. d, Densitometric quantification of FGF21 normalized to LC at 4 h and 16 h after injection; ns, not significant; P < 0.05. e,g, Serum <t>GDF15</t> measured 4 h and 16 h after VEH or BAY injection at ZT0 ( e ; sampling at ZT4 and ZT16) or ZT12 ( g ; sampling at ZT16 and ZT4), respectively. n=4/group/timepoint. f,h, Daily water intake following injections at ZT0 ( f ) or ZT12 ( h ). n=8/group/timepoint. Data are mean ± s.e.m. Statistical comparisons were performed between VEH and BAY at each matched time point; ns, not significant; * P < 0.05. All experiments were performed in male C57BL/6J mice.
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    R&D Systems gdf15 elisa
    Circulating <t>GDF15</t> levels increase in individuals with PBH after a mixed meal (A) Experimental design. Blood samples were collected from 15 individuals with PBH, 15 asymptomatic (Asx) individuals, and 10 overweight/obese (Ow/Ob) controls at 0, 30, and 120 min during a mixed-meal test. (B) Plasma glucose measured by yellow springs instruments (YSI). (C) Glucose nadir. (D–G) Plasma insulin, C-peptide, GLP-1, and GDF15 measured by ELISA. (H–P) Pearson correlation analyses between GDF15 and plama glucose (H–J), insulin (K–M), and GLP-1 (N–P) at fasting state, 30 min, and 120 min after meal digestion. Data are represented as mean ± SD. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗ p < 0.0001.
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    Circulating <t>GDF15</t> levels increase in individuals with PBH after a mixed meal (A) Experimental design. Blood samples were collected from 15 individuals with PBH, 15 asymptomatic (Asx) individuals, and 10 overweight/obese (Ow/Ob) controls at 0, 30, and 120 min during a mixed-meal test. (B) Plasma glucose measured by yellow springs instruments (YSI). (C) Glucose nadir. (D–G) Plasma insulin, C-peptide, GLP-1, and GDF15 measured by ELISA. (H–P) Pearson correlation analyses between GDF15 and plama glucose (H–J), insulin (K–M), and GLP-1 (N–P) at fasting state, 30 min, and 120 min after meal digestion. Data are represented as mean ± SD. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗ p < 0.0001.
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    Image Search Results


    a, Daily food intake (g per mouse) measured in HFD-fed mice receiving daily intraperitoneal injections of vehicle (VEH) or BAY2402234 (BAY) at ZT0 or ZT12 for 7 consecutive days (n=20/group). b, Distribution of food intake between light and dark phases for the same conditions as in ( a) (n=4 cages/group). c, Representative immunoblots of hepatic FGF21 collected 4 h and 16 h after VEH or BAY injection at ZT0 (top) or ZT12 (bottom). LC, loading control. n=4/group/timepoint. d, Densitometric quantification of FGF21 normalized to LC at 4 h and 16 h after injection; ns, not significant; P < 0.05. e,g, Serum GDF15 measured 4 h and 16 h after VEH or BAY injection at ZT0 ( e ; sampling at ZT4 and ZT16) or ZT12 ( g ; sampling at ZT16 and ZT4), respectively. n=4/group/timepoint. f,h, Daily water intake following injections at ZT0 ( f ) or ZT12 ( h ). n=8/group/timepoint. Data are mean ± s.e.m. Statistical comparisons were performed between VEH and BAY at each matched time point; ns, not significant; * P < 0.05. All experiments were performed in male C57BL/6J mice.

    Journal: bioRxiv

    Article Title: Chronopharmacological targeting of mitochondrial dihydroorotate dehydrogenase prevents diet-induced obesity in male mice

    doi: 10.64898/2026.04.18.719366

    Figure Lengend Snippet: a, Daily food intake (g per mouse) measured in HFD-fed mice receiving daily intraperitoneal injections of vehicle (VEH) or BAY2402234 (BAY) at ZT0 or ZT12 for 7 consecutive days (n=20/group). b, Distribution of food intake between light and dark phases for the same conditions as in ( a) (n=4 cages/group). c, Representative immunoblots of hepatic FGF21 collected 4 h and 16 h after VEH or BAY injection at ZT0 (top) or ZT12 (bottom). LC, loading control. n=4/group/timepoint. d, Densitometric quantification of FGF21 normalized to LC at 4 h and 16 h after injection; ns, not significant; P < 0.05. e,g, Serum GDF15 measured 4 h and 16 h after VEH or BAY injection at ZT0 ( e ; sampling at ZT4 and ZT16) or ZT12 ( g ; sampling at ZT16 and ZT4), respectively. n=4/group/timepoint. f,h, Daily water intake following injections at ZT0 ( f ) or ZT12 ( h ). n=8/group/timepoint. Data are mean ± s.e.m. Statistical comparisons were performed between VEH and BAY at each matched time point; ns, not significant; * P < 0.05. All experiments were performed in male C57BL/6J mice.

    Article Snippet: Serum GDF15 was measured with Mouse/Rat GDF15 Quantikine ELISA Kit (R&D Systems), following the manufacturer recommendations.

    Techniques: Western Blot, Injection, Control, Sampling

    Circulating GDF15 levels increase in individuals with PBH after a mixed meal (A) Experimental design. Blood samples were collected from 15 individuals with PBH, 15 asymptomatic (Asx) individuals, and 10 overweight/obese (Ow/Ob) controls at 0, 30, and 120 min during a mixed-meal test. (B) Plasma glucose measured by yellow springs instruments (YSI). (C) Glucose nadir. (D–G) Plasma insulin, C-peptide, GLP-1, and GDF15 measured by ELISA. (H–P) Pearson correlation analyses between GDF15 and plama glucose (H–J), insulin (K–M), and GLP-1 (N–P) at fasting state, 30 min, and 120 min after meal digestion. Data are represented as mean ± SD. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗ p < 0.0001.

    Journal: Cell Reports Medicine

    Article Title: Plasma GDF15 increases during hyperinsulinemic hypoglycemia in humans with post-bariatric hypoglycemia and after insulin exposure in mice

    doi: 10.1016/j.xcrm.2026.102656

    Figure Lengend Snippet: Circulating GDF15 levels increase in individuals with PBH after a mixed meal (A) Experimental design. Blood samples were collected from 15 individuals with PBH, 15 asymptomatic (Asx) individuals, and 10 overweight/obese (Ow/Ob) controls at 0, 30, and 120 min during a mixed-meal test. (B) Plasma glucose measured by yellow springs instruments (YSI). (C) Glucose nadir. (D–G) Plasma insulin, C-peptide, GLP-1, and GDF15 measured by ELISA. (H–P) Pearson correlation analyses between GDF15 and plama glucose (H–J), insulin (K–M), and GLP-1 (N–P) at fasting state, 30 min, and 120 min after meal digestion. Data are represented as mean ± SD. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗ p < 0.0001.

    Article Snippet: GDF15 ELISA (R&D systems, Minneapolis, MN, USA, MGD150) was performed on plasma samples according to manufacturer’s instructions.

    Techniques: Clinical Proteomics, Enzyme-linked Immunosorbent Assay

    GDF15 levels are elevated in PBH individuals during hypoglycemia induced by hyperinsulinemic hypoglycemic clamp (A) Experimental design. Blood samples were collected from 15 PBH, 15 Asx, and 10 Ow/Ob patients at time 0, 40, 90, 110, and 120 min during hyperinsulinemic hypoglycemic clamp. (B) Plasma glucose. (C) Plasma epinephrine. (D) Plasma norepinephrine. (E) Plasma GDF15. (F–H) Pearson correlation between glucose and GDF15. (I–K) Pearson correlation between epinephrine and GDF15. For all panels, asterisks denote significant difference between PBH vs. Ow/Ob (blue color), between PBH vs. Asx (green), or between PBH vs. Asx (orange). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗ p < 0.0001. Data are represented as mean ± SD.

    Journal: Cell Reports Medicine

    Article Title: Plasma GDF15 increases during hyperinsulinemic hypoglycemia in humans with post-bariatric hypoglycemia and after insulin exposure in mice

    doi: 10.1016/j.xcrm.2026.102656

    Figure Lengend Snippet: GDF15 levels are elevated in PBH individuals during hypoglycemia induced by hyperinsulinemic hypoglycemic clamp (A) Experimental design. Blood samples were collected from 15 PBH, 15 Asx, and 10 Ow/Ob patients at time 0, 40, 90, 110, and 120 min during hyperinsulinemic hypoglycemic clamp. (B) Plasma glucose. (C) Plasma epinephrine. (D) Plasma norepinephrine. (E) Plasma GDF15. (F–H) Pearson correlation between glucose and GDF15. (I–K) Pearson correlation between epinephrine and GDF15. For all panels, asterisks denote significant difference between PBH vs. Ow/Ob (blue color), between PBH vs. Asx (green), or between PBH vs. Asx (orange). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗ p < 0.0001. Data are represented as mean ± SD.

    Article Snippet: GDF15 ELISA (R&D systems, Minneapolis, MN, USA, MGD150) was performed on plasma samples according to manufacturer’s instructions.

    Techniques: Clinical Proteomics

    Heatmap showing correlations between GDF15 levels and hypoglycemia symptoms (Edinburgh Hypoglycemia Symptom Scale) during the hyperinsulinemic hypoglycemic clamp An asterisk (∗) indicates a significant correlation between the symptom and GDF15 levels during the hypoglycemic clamp (Pearson correlation, p < 0.05). Data include 15 individuals with PBH, 15 Asx, and 10 Ow/Ob, assessed at 0, 40, 90, and 110 min.

    Journal: Cell Reports Medicine

    Article Title: Plasma GDF15 increases during hyperinsulinemic hypoglycemia in humans with post-bariatric hypoglycemia and after insulin exposure in mice

    doi: 10.1016/j.xcrm.2026.102656

    Figure Lengend Snippet: Heatmap showing correlations between GDF15 levels and hypoglycemia symptoms (Edinburgh Hypoglycemia Symptom Scale) during the hyperinsulinemic hypoglycemic clamp An asterisk (∗) indicates a significant correlation between the symptom and GDF15 levels during the hypoglycemic clamp (Pearson correlation, p < 0.05). Data include 15 individuals with PBH, 15 Asx, and 10 Ow/Ob, assessed at 0, 40, 90, and 110 min.

    Article Snippet: GDF15 ELISA (R&D systems, Minneapolis, MN, USA, MGD150) was performed on plasma samples according to manufacturer’s instructions.

    Techniques:

    GDF15 levels are increased with insulin-induced hypoglycemia, and exogenous GDF15 inhibits food intake after meal-stimulated hypoglycemia (A) Experimental design for (B and C) ( n = 10 per group). (B and C) (B) Blood glucose and (C) plasma GDF15. (D–F) Pearson correlation between glucose and GDF15. (G) Schematic of the insulin-augmented mixed meal tolerance test ( n = 5 per group). (H and I) (H) Blood glucose and (I) body weight after GDF15 or saline treatment. (J) Blood glucose in male mice ( n = 5 per group). (K) Food intake during insulin-induced hypoglycemia in male mice. (L) Blood glucose in female mice ( n = 5 per group). (M) Food intake during insulin-induced hypoglycemia in female mice. In all panels, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001 by two-way ANOVA with Tukey’s multiple-comparison test. Data are presented as mean ± SD from two independent experiments.

    Journal: Cell Reports Medicine

    Article Title: Plasma GDF15 increases during hyperinsulinemic hypoglycemia in humans with post-bariatric hypoglycemia and after insulin exposure in mice

    doi: 10.1016/j.xcrm.2026.102656

    Figure Lengend Snippet: GDF15 levels are increased with insulin-induced hypoglycemia, and exogenous GDF15 inhibits food intake after meal-stimulated hypoglycemia (A) Experimental design for (B and C) ( n = 10 per group). (B and C) (B) Blood glucose and (C) plasma GDF15. (D–F) Pearson correlation between glucose and GDF15. (G) Schematic of the insulin-augmented mixed meal tolerance test ( n = 5 per group). (H and I) (H) Blood glucose and (I) body weight after GDF15 or saline treatment. (J) Blood glucose in male mice ( n = 5 per group). (K) Food intake during insulin-induced hypoglycemia in male mice. (L) Blood glucose in female mice ( n = 5 per group). (M) Food intake during insulin-induced hypoglycemia in female mice. In all panels, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001 by two-way ANOVA with Tukey’s multiple-comparison test. Data are presented as mean ± SD from two independent experiments.

    Article Snippet: GDF15 ELISA (R&D systems, Minneapolis, MN, USA, MGD150) was performed on plasma samples according to manufacturer’s instructions.

    Techniques: Clinical Proteomics, Saline, Comparison