Glut4 Antibody (3G10A3) - BSA Free
Novus Biologicals | Catalog # NBP2-22214
Key Product Details
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Immunogen
Reactivity Notes
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Theoretical MW
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for Glut4 Antibody (3G10A3) - BSA Free
Western Blot: Glut4 Antibody (3G10A3)BSA Free [NBP2-22214]
Western Blot: Glut4 Antibody (3G10A3) [NBP2-22214] - Western blot analysis using Glucose Transporter GLUT4 mouse mAb against HeLa (1), NIH3T3 (2), 3T3-L1 (3) cell lysate and Mouse heart (4) tissue lysate.Immunocytochemistry/ Immunofluorescence: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214]
Immunocytochemistry/Immunofluorescence: Glut4 Antibody (3G10A3) [NBP2-22214] - Analysis of HepG2 cells using Glucose Transporter GLUT4 mouse mAb (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.Immunohistochemistry-Paraffin: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214]
Immunohistochemistry-Paraffin: Glut4 Antibody (3G10A3) [NBP2-22214] - analysis of cardiac muscle tissues using SLC2A4 mouse mAb with DAB staining.Flow Cytometry: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214]
Flow Cytometry: Glut4 Antibody (3G10A3) [NBP2-22214] - Flow cytometric analysis of HeLa cells using Glucose Transporter GLUT4 mouse mAb (green) and negative control (purple).Western Blot: Glut4 Antibody (3G10A3)BSA Free [NBP2-22214]
Western Blot: Glut4 Antibody (3G10A3) [NBP2-22214] - Western blot analysis using Glucose Transporter Glut4 Antibody (3G10A3)mAb against HEK293 (1) and Glucose Transporter GLUT4 (AA: 224-353)-hIgGFc transfected HEK293 (2) cell lysate.Western Blot: Glut4 Antibody (3G10A3)BSA Free [NBP2-22214]
Western Blot: Glut4 Antibody (3G10A3) [NBP2-22214] - human Glucose Transporter GLUT4 recombinant protein.Immunocytochemistry/ Immunofluorescence: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214]
Immunocytochemistry/Immunofluorescence: Glut4 Antibody (3G10A3) [NBP2-22214] - Analysis of HeLa cells using Glucose Transporter GLUT4 mouse mAb (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.Immunohistochemistry-Paraffin: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214]
Immunohistochemistry-Paraffin: Glut4 Antibody (3G10A3) [NBP2-22214] - Analysis of paraffin-embedded bladder cancer tissues using Glucose Transporter GLUT4 mouse mAb with DAB staining.ELISA: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214]
ELISA: Glut4 Antibody (3G10A3) [NBP2-22214] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng)Western Blot: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214] -
Supporting data 2 for Figure 1.(A-B) Body weight (A) and fasting glucose levels (B) of mice fed a HFD for 0, 1, 2, or 4 weeks. One-way ANOVA compared to 0 week HFD-fed mice, **p<0.01, ***p<0.001, ****p<0.0001. n=10 (C) ITT on mice fed a HFD for 0, 1, 2, 4 weeks, and mice fed 2 week HFD and 2 week ND. The mice were fasted for 6 hours and injected with insulin (0.75 U/kg body weight). One-way ANOVA, *p<0.05. n=8 (0 week ND), 10 (1 week HFD), 10 (2 week HFD), 10 (2 week HFD), and 6 (2 week HFD +2 week ND). (D–F) Immunoblots of vWAT(D), sWAT(E), and BAT (F) from mice fed a HFD for 0, 1, 2, or 4 weeks. Mice were fasted for 6 hours and injected with insulin (0.75 U/kg body weight). n=5. See Figure 1—figure supplement 2—source data 1.Figure 1—figure supplement 2—source data 1.Uncropped blots and source data for graphs for Figure 1—figure supplement 2.Uncropped blots and source data for graphs for Figure 1—figure supplement 2. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36920797), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214] -
Supporting data 2 for Figure 1.(A-B) Body weight (A) and fasting glucose levels (B) of mice fed a HFD for 0, 1, 2, or 4 weeks. One-way ANOVA compared to 0 week HFD-fed mice, **p<0.01, ***p<0.001, ****p<0.0001. n=10 (C) ITT on mice fed a HFD for 0, 1, 2, 4 weeks, and mice fed 2 week HFD and 2 week ND. The mice were fasted for 6 hours and injected with insulin (0.75 U/kg body weight). One-way ANOVA, *p<0.05. n=8 (0 week ND), 10 (1 week HFD), 10 (2 week HFD), 10 (2 week HFD), and 6 (2 week HFD +2 week ND). (D–F) Immunoblots of vWAT(D), sWAT(E), and BAT (F) from mice fed a HFD for 0, 1, 2, or 4 weeks. Mice were fasted for 6 hours and injected with insulin (0.75 U/kg body weight). n=5. See Figure 1—figure supplement 2—source data 1.Figure 1—figure supplement 2—source data 1.Uncropped blots and source data for graphs for Figure 1—figure supplement 2.Uncropped blots and source data for graphs for Figure 1—figure supplement 2. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36920797), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214] -
Supporting data 2 for Figure 1.(A-B) Body weight (A) and fasting glucose levels (B) of mice fed a HFD for 0, 1, 2, or 4 weeks. One-way ANOVA compared to 0 week HFD-fed mice, **p<0.01, ***p<0.001, ****p<0.0001. n=10 (C) ITT on mice fed a HFD for 0, 1, 2, 4 weeks, and mice fed 2 week HFD and 2 week ND. The mice were fasted for 6 hours and injected with insulin (0.75 U/kg body weight). One-way ANOVA, *p<0.05. n=8 (0 week ND), 10 (1 week HFD), 10 (2 week HFD), 10 (2 week HFD), and 6 (2 week HFD +2 week ND). (D–F) Immunoblots of vWAT(D), sWAT(E), and BAT (F) from mice fed a HFD for 0, 1, 2, or 4 weeks. Mice were fasted for 6 hours and injected with insulin (0.75 U/kg body weight). n=5. See Figure 1—figure supplement 2—source data 1.Figure 1—figure supplement 2—source data 1.Uncropped blots and source data for graphs for Figure 1—figure supplement 2.Uncropped blots and source data for graphs for Figure 1—figure supplement 2. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36920797), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Glut4 Antibody (3G10A3) - BSA Free [NBP2-22214] -
mTORC2 in adipose tissue is required for cold‐induced glucose uptake and glycolysis2‐deoxyglucose‐6‐phosphate (2DG6P) accumulation in BAT of AdRiKO and control mice housed at 22 or at 4C for 4 h (n = 6/group).Extracellular acidification rate (ECAR) of BAT explants from AdRiKO and control mice housed at 22 or at 4C for 4 h (n = 7/group).Immunoblot analysis of BAT from AdRiKO and control mice housed at 22 or at 4C for 8 h for the indicated proteins (n = 6/group, each lane represents a mix of 3 mice).Immunoblot analysis of isolated plasma membranes from BAT of AdRiKO and control mice housed at 22 or at 4C for 8 h for the indicated proteins (n = 6/group, each lane represents a mix of 3 mice).Immunoblot analysis of mitochondrial and cytosolic fractions from BAT of AdRiKO and control mice housed at 22 or at 4C for 4 h for the indicated proteins (n = 6/group, each lane represents a mix of 3 mice).Cytosolic hexokinase activity in BAT of AdRiKO and control mice housed at 22 or at 4C for 4 h [n = 5 (control 22C), n = 5 (AdRiKO 22C), n = 7 (control 4C), n = 7 (AdRiKO 4C)].Mitochondrial hexokinase activity in BAT of AdRiKO and control mice housed at 22 or at 4C for 4 h [n = 5 (control 22C), n = 5 (AdRiKO 22C), n = 7 (control 4C), n = 7 (AdRiKO 4C)].Data information: Data represent mean +/- SEM. Statistically significant differences between AdRiKO and control mice were determined with unpaired Student's t‐test and are indicated with asterisks (*P < 0.05). Statistically significant differences between temperatures were determined with unpaired Student's t‐test and are indicated with a number sign (#P < 0.05; ##P < 0.01; ###P < 0.001). The exact P‐value for each significant difference can be found in Appendix Table S2. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/26772600), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for Glut4 Antibody (3G10A3) - BSA Free
ELISA
Flow Cytometry
Immunocytochemistry/ Immunofluorescence
Immunohistochemistry
Immunohistochemistry-Paraffin
Western Blot
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Advanced Features
- Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
- Spillover Popups - Visualize the spectra of individual fluorochromes
- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
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Background: Glut4
Alternate Names
Gene Symbol
Additional Glut4 Products
Product Documents for Glut4 Antibody (3G10A3) - BSA Free
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Product Specific Notices for Glut4 Antibody (3G10A3) - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- 7-Amino Actinomycin D (7-AAD) Cell Viability Flow Cytometry Protocol
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
- Extracellular Membrane Flow Cytometry Protocol
- Flow Cytometry Protocol for Cell Surface Markers
- Flow Cytometry Protocol for Staining Membrane Associated Proteins
- Flow Cytometry Staining Protocols
- Flow Cytometry Troubleshooting Guide
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- How to Run an R&D Systems DuoSet ELISA
- How to Run an R&D Systems Quantikine ELISA
- How to Run an R&D Systems Quantikine™ QuicKit™ ELISA
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Intracellular Flow Cytometry Protocol Using Alcohol (Methanol)
- Intracellular Flow Cytometry Protocol Using Detergents
- Intracellular Nuclear Staining Flow Cytometry Protocol Using Detergents
- Intracellular Staining Flow Cytometry Protocol Using Alcohol Permeabilization
- Intracellular Staining Flow Cytometry Protocol Using Detergents to Permeabilize Cells
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Propidium Iodide Cell Viability Flow Cytometry Protocol
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Liperfluo
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Characterization of Human Th22 Cells
- Protocol for the Characterization of Human Th9 Cells
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- Quantikine HS ELISA Kit Assay Principle, Alkaline Phosphatase
- Quantikine HS ELISA Kit Principle, Streptavidin-HRP Polymer
- R&D Systems Quality Control Western Blot Protocol
- Sandwich ELISA (Colorimetric) – Biotin/Streptavidin Detection Protocol
- Sandwich ELISA (Colorimetric) – Direct Detection Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: ELISA
- Troubleshooting Guide: Fluorokine Flow Cytometry Kits
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars