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mouse monoclonal anti glut4  (Proteintech)


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    Proteintech mouse monoclonal anti glut4
    Mouse Monoclonal Anti Glut4, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 202 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+glut4+monoclonal+antibody/10__1530_slash_ec___25___0430-329-28-33?v=Proteintech
    Average 96 stars, based on 202 article reviews
    mouse monoclonal anti glut4 - by Bioz Stars, 2026-08
    96/100 stars

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    Effect of Andrographis paniculata on <t>glucose</t> <t>transporter</t> <t>4</t> (GLUT 4) expression (A) and numerical data representing GLUT 4 expression (B). Data are expressed as mean ± SD for 10 rats per group and analyzed by unpaired T -test. * p < 0.05 vs. control.
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    Effect of Andrographis paniculata on <t>glucose</t> <t>transporter</t> <t>4</t> (GLUT 4) expression (A) and numerical data representing GLUT 4 expression (B). Data are expressed as mean ± SD for 10 rats per group and analyzed by unpaired T -test. * p < 0.05 vs. control.
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    Figure 5. Effect of gintonin on <t>GLUT4</t> expression in total lysates and plasma membrane fractions of C2C12 myotubes. (A) GLUT4 expression in total lysates. (B) GLUT4 expression in the plasma membrane fraction. C2C12 myotubes were treated with gintonin (GT, 10 µg/mL) for 120 min or insulin (INS, 100 nM) for 30 min. GLUT4 expression in total lysates and plasma membrane fraction of C2C12 myotubes was detected by immunoblotting. β-actin and Na+/K+ ATPase were also detected as loading controls. All data are shown as the mean ± SEM (n = 4); ** p < 0.01; *** p < 0.001 vs. untreated control cells (Con). Original western blot images can be found in Supplementary File S1.
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    Figure 5. Effect of gintonin on <t>GLUT4</t> expression in total lysates and plasma membrane fractions of C2C12 myotubes. (A) GLUT4 expression in total lysates. (B) GLUT4 expression in the plasma membrane fraction. C2C12 myotubes were treated with gintonin (GT, 10 µg/mL) for 120 min or insulin (INS, 100 nM) for 30 min. GLUT4 expression in total lysates and plasma membrane fraction of C2C12 myotubes was detected by immunoblotting. β-actin and Na+/K+ ATPase were also detected as loading controls. All data are shown as the mean ± SEM (n = 4); ** p < 0.01; *** p < 0.001 vs. untreated control cells (Con). Original western blot images can be found in Supplementary File S1.
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    Figure 5. Effect of gintonin on <t>GLUT4</t> expression in total lysates and plasma membrane fractions of C2C12 myotubes. (A) GLUT4 expression in total lysates. (B) GLUT4 expression in the plasma membrane fraction. C2C12 myotubes were treated with gintonin (GT, 10 µg/mL) for 120 min or insulin (INS, 100 nM) for 30 min. GLUT4 expression in total lysates and plasma membrane fraction of C2C12 myotubes was detected by immunoblotting. β-actin and Na+/K+ ATPase were also detected as loading controls. All data are shown as the mean ± SEM (n = 4); ** p < 0.01; *** p < 0.001 vs. untreated control cells (Con). Original western blot images can be found in Supplementary File S1.
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    Proteintech mouse anti glut4 monoclonal antibody
    ZnT 3 deletion is associated with a significant impairment of insulin signaling in the hippocampus. (A) Body mass analysis of ZnT 3 - / - and WT mice. *, ### Denote significant difference between groups indicated by the connector lines, p < 0.05, p < 0.001, two-way ANOVA with LSD post-hoc test. (B) Brain weight analysis of ZnT 3 - / - and WT mice. Two-way ANOVA with LSD post-hoc test. (C, D) The blood glucose levels in male (C) and female (D) mice (ZnT 3 - / - ; and WT) after fasting; n = 6 for both ZnT 3 - / - and n = 5 for both WT groups. Two-way ANOVA with LSD post-hoc test. (E, F) mRNA expression levels of Slc2a1 (GLUT1), Slc2a3 (GLUT3), and Slc2a4 <t>(GLUT4)</t> in cortex (E) ; and Slc2a1 (GLUT1), Slc2a3 (GLUT3), and Slc2a4 (GLUT4) and Insr (INSR) in hippocampus (F) . Expression levels are normalized to housekeeping gene Gapdh . * Denotes significant difference between groups indicated by the connector lines, p < 0.05, Mann-Whitney test. (G, H) Immunofluorescence staining of hippocampal sections of 9-months old mice. (G) : GLUT3-(red), DAPI-(blue) and GFAP (green). (H) : GLUT4-(green), DAPI-(blue) and NeuN (red). Scale bar, 50 μm; Zoom Scale bar, 5 μm. (I, J) Statistical analysis of images as those shown in (G) and (H) . * Denotes significant difference between groups indicated by the connector lines, p < 0.05, Mann-Whitney test.
    Mouse Anti Glut4 Monoclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 96 stars, based on 1 article reviews
    mouse anti glut4 monoclonal antibody - by Bioz Stars, 2026-08
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    Cell Signaling Technology Inc mouse monoclonal glut4
    ZnT 3 deletion is associated with a significant impairment of insulin signaling in the hippocampus. (A) Body mass analysis of ZnT 3 - / - and WT mice. *, ### Denote significant difference between groups indicated by the connector lines, p < 0.05, p < 0.001, two-way ANOVA with LSD post-hoc test. (B) Brain weight analysis of ZnT 3 - / - and WT mice. Two-way ANOVA with LSD post-hoc test. (C, D) The blood glucose levels in male (C) and female (D) mice (ZnT 3 - / - ; and WT) after fasting; n = 6 for both ZnT 3 - / - and n = 5 for both WT groups. Two-way ANOVA with LSD post-hoc test. (E, F) mRNA expression levels of Slc2a1 (GLUT1), Slc2a3 (GLUT3), and Slc2a4 <t>(GLUT4)</t> in cortex (E) ; and Slc2a1 (GLUT1), Slc2a3 (GLUT3), and Slc2a4 (GLUT4) and Insr (INSR) in hippocampus (F) . Expression levels are normalized to housekeeping gene Gapdh . * Denotes significant difference between groups indicated by the connector lines, p < 0.05, Mann-Whitney test. (G, H) Immunofluorescence staining of hippocampal sections of 9-months old mice. (G) : GLUT3-(red), DAPI-(blue) and GFAP (green). (H) : GLUT4-(green), DAPI-(blue) and NeuN (red). Scale bar, 50 μm; Zoom Scale bar, 5 μm. (I, J) Statistical analysis of images as those shown in (G) and (H) . * Denotes significant difference between groups indicated by the connector lines, p < 0.05, Mann-Whitney test.
    Mouse Monoclonal Glut4, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+glut4+monoclonal+antibody/pm37714510-337-42-50?v=Cell+Signaling+Technology+Inc
    Average 96 stars, based on 1 article reviews
    mouse monoclonal glut4 - by Bioz Stars, 2026-08
    96/100 stars
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    Image Search Results


    Effect of Andrographis paniculata on glucose transporter 4 (GLUT 4) expression (A) and numerical data representing GLUT 4 expression (B). Data are expressed as mean ± SD for 10 rats per group and analyzed by unpaired T -test. * p < 0.05 vs. control.

    Journal: Frontiers in Nutrition

    Article Title: Andrographis paniculata improves glucose regulation by enhancing insulin sensitivity and upregulating GLUT 4 expression in Wistar rats

    doi: 10.3389/fnut.2024.1416641

    Figure Lengend Snippet: Effect of Andrographis paniculata on glucose transporter 4 (GLUT 4) expression (A) and numerical data representing GLUT 4 expression (B). Data are expressed as mean ± SD for 10 rats per group and analyzed by unpaired T -test. * p < 0.05 vs. control.

    Article Snippet: The procedures were performed using Thermo Fischer Kit (Thermo Fischer Scientific Inc., USA) and anti-mouse GLUT4 monoclonal for GLUT4 expression (Thermo Fischer Scientific Inc., USA).

    Techniques: Expressing, Control

    Figure 5. Effect of gintonin on GLUT4 expression in total lysates and plasma membrane fractions of C2C12 myotubes. (A) GLUT4 expression in total lysates. (B) GLUT4 expression in the plasma membrane fraction. C2C12 myotubes were treated with gintonin (GT, 10 µg/mL) for 120 min or insulin (INS, 100 nM) for 30 min. GLUT4 expression in total lysates and plasma membrane fraction of C2C12 myotubes was detected by immunoblotting. β-actin and Na+/K+ ATPase were also detected as loading controls. All data are shown as the mean ± SEM (n = 4); ** p < 0.01; *** p < 0.001 vs. untreated control cells (Con). Original western blot images can be found in Supplementary File S1.

    Journal: Biomolecules

    Article Title: Gintonin Stimulates Glucose Uptake in Myocytes: Involvement of Calcium and Extracellular Signal-Regulated Kinase Signaling.

    doi: 10.3390/biom14101316

    Figure Lengend Snippet: Figure 5. Effect of gintonin on GLUT4 expression in total lysates and plasma membrane fractions of C2C12 myotubes. (A) GLUT4 expression in total lysates. (B) GLUT4 expression in the plasma membrane fraction. C2C12 myotubes were treated with gintonin (GT, 10 µg/mL) for 120 min or insulin (INS, 100 nM) for 30 min. GLUT4 expression in total lysates and plasma membrane fraction of C2C12 myotubes was detected by immunoblotting. β-actin and Na+/K+ ATPase were also detected as loading controls. All data are shown as the mean ± SEM (n = 4); ** p < 0.01; *** p < 0.001 vs. untreated control cells (Con). Original western blot images can be found in Supplementary File S1.

    Article Snippet: The cell membrane fraction and total cell lysate were also used to measure GLUT4 expression by immunoblotting using a mouse anti-GLUT4 monoclonal antibody (Santa Cruz Biotechnology) and a goat anti-mouse IgG antibody conjugated to HRP (Santa Cruz Biotechnology).

    Techniques: Expressing, Clinical Proteomics, Membrane, Western Blot, Control

    Figure 6. Possible signaling pathways of gintonin (GT)-induced glucose uptake in C2C12 myotubes. Gintonin induces transient increases in intracellular calcium concentrations and ERK activation via LPA receptor (LPAR) activation. These may lead to increases in the expression and translocation of GLUT4, subsequently increasing glucose uptake. PLC, phospholipase C; ERK, extracellular signal-regulated kinase; GLUT4, glucose transporter type 4.

    Journal: Biomolecules

    Article Title: Gintonin Stimulates Glucose Uptake in Myocytes: Involvement of Calcium and Extracellular Signal-Regulated Kinase Signaling.

    doi: 10.3390/biom14101316

    Figure Lengend Snippet: Figure 6. Possible signaling pathways of gintonin (GT)-induced glucose uptake in C2C12 myotubes. Gintonin induces transient increases in intracellular calcium concentrations and ERK activation via LPA receptor (LPAR) activation. These may lead to increases in the expression and translocation of GLUT4, subsequently increasing glucose uptake. PLC, phospholipase C; ERK, extracellular signal-regulated kinase; GLUT4, glucose transporter type 4.

    Article Snippet: The cell membrane fraction and total cell lysate were also used to measure GLUT4 expression by immunoblotting using a mouse anti-GLUT4 monoclonal antibody (Santa Cruz Biotechnology) and a goat anti-mouse IgG antibody conjugated to HRP (Santa Cruz Biotechnology).

    Techniques: Protein-Protein interactions, Activation Assay, Expressing, Translocation Assay

    ZnT 3 deletion is associated with a significant impairment of insulin signaling in the hippocampus. (A) Body mass analysis of ZnT 3 - / - and WT mice. *, ### Denote significant difference between groups indicated by the connector lines, p < 0.05, p < 0.001, two-way ANOVA with LSD post-hoc test. (B) Brain weight analysis of ZnT 3 - / - and WT mice. Two-way ANOVA with LSD post-hoc test. (C, D) The blood glucose levels in male (C) and female (D) mice (ZnT 3 - / - ; and WT) after fasting; n = 6 for both ZnT 3 - / - and n = 5 for both WT groups. Two-way ANOVA with LSD post-hoc test. (E, F) mRNA expression levels of Slc2a1 (GLUT1), Slc2a3 (GLUT3), and Slc2a4 (GLUT4) in cortex (E) ; and Slc2a1 (GLUT1), Slc2a3 (GLUT3), and Slc2a4 (GLUT4) and Insr (INSR) in hippocampus (F) . Expression levels are normalized to housekeeping gene Gapdh . * Denotes significant difference between groups indicated by the connector lines, p < 0.05, Mann-Whitney test. (G, H) Immunofluorescence staining of hippocampal sections of 9-months old mice. (G) : GLUT3-(red), DAPI-(blue) and GFAP (green). (H) : GLUT4-(green), DAPI-(blue) and NeuN (red). Scale bar, 50 μm; Zoom Scale bar, 5 μm. (I, J) Statistical analysis of images as those shown in (G) and (H) . * Denotes significant difference between groups indicated by the connector lines, p < 0.05, Mann-Whitney test.

    Journal: Frontiers in Molecular Neuroscience

    Article Title: Genetic deletion of zinc transporter ZnT 3 induces progressive cognitive deficits in mice by impairing dendritic spine plasticity and glucose metabolism

    doi: 10.3389/fnmol.2024.1375925

    Figure Lengend Snippet: ZnT 3 deletion is associated with a significant impairment of insulin signaling in the hippocampus. (A) Body mass analysis of ZnT 3 - / - and WT mice. *, ### Denote significant difference between groups indicated by the connector lines, p < 0.05, p < 0.001, two-way ANOVA with LSD post-hoc test. (B) Brain weight analysis of ZnT 3 - / - and WT mice. Two-way ANOVA with LSD post-hoc test. (C, D) The blood glucose levels in male (C) and female (D) mice (ZnT 3 - / - ; and WT) after fasting; n = 6 for both ZnT 3 - / - and n = 5 for both WT groups. Two-way ANOVA with LSD post-hoc test. (E, F) mRNA expression levels of Slc2a1 (GLUT1), Slc2a3 (GLUT3), and Slc2a4 (GLUT4) in cortex (E) ; and Slc2a1 (GLUT1), Slc2a3 (GLUT3), and Slc2a4 (GLUT4) and Insr (INSR) in hippocampus (F) . Expression levels are normalized to housekeeping gene Gapdh . * Denotes significant difference between groups indicated by the connector lines, p < 0.05, Mann-Whitney test. (G, H) Immunofluorescence staining of hippocampal sections of 9-months old mice. (G) : GLUT3-(red), DAPI-(blue) and GFAP (green). (H) : GLUT4-(green), DAPI-(blue) and NeuN (red). Scale bar, 50 μm; Zoom Scale bar, 5 μm. (I, J) Statistical analysis of images as those shown in (G) and (H) . * Denotes significant difference between groups indicated by the connector lines, p < 0.05, Mann-Whitney test.

    Article Snippet: The following primary antibodies were used: rabbit anti-GLUT3 ployclonal antibody (20403-1-AP, Proteintech, USA; 1:2,000); mouse anti-GLUT4 monoclonal antibody (66846-1-lg, Proteintech, USA; 1:2,000); rabbit anti-GSK-3β monoclonal antibody (D5C5Z, Cell Signaling, USA; 1:1,000); and anti-GAPDH recombinant rabbit monoclonal antibody (SA30-01, HUABIO, China; 1:5,000).

    Techniques: Expressing, MANN-WHITNEY, Immunofluorescence, Staining