Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal Glucose Transporter GLUT4 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB, IP, Dot and reacts with Human, Mouse, Rat, Transfected cell lysate - Human samples.
View Alternative Names
Glut4, Slc2a4, GT2, GLUT-4
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling SLC2A4 with ab313775 at 1/5000 (0.104 µg/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : No staining on human liver. The section was incubated with ab313775 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human skeletal muscle tissue labeling SLC2A4 with ab313775 at 1/5000 (0.104 µg/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on human skeletal muscle. The section was incubated with ab313775 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling SLC2A4 with ab313775 at 1/5000 (0.104 µg/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : No staining on mouse liver. The section was incubated with ab313775 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat skeletal muscle tissue labeling SLC2A4 with ab313775 at 1/5000 (0.104 µg/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on rat skeletal muscle. The section was incubated with ab313775 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat cardiac muscle tissue labeling SLC2A4 with ab313775 at 1/5000 (0.104 µg/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on rat cardiac muscle. The section was incubated with ab313775 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized 3T3-L1 (mouse embryonic fibroblast) cells labelling SLC2A4 with ab313775 at 1/100 (5.18 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 µg/ml) dilution (Green). Confocal image showing cytoplasmic staining in differentiated 3T3-L1 cells, and no staining in 3T3-L1 cells. Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8) ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5 µg/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 µg/ml) dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labeling SLC2A4 with ab313775 at 1/5000 (0.104 µg/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on mouse skeletal muscle (PMID : 2654938; PMID : 23877319; PMID : 33061888). The section was incubated with ab313775 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling SLC2A4 with ab313775 at 1/5000 (0.104 µg/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : No staining on rat liver. The section was incubated with ab313775 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation.
SLC2A4 was immunoprecipitated from 0.35 mg Mouse heart tissue lysate with ab313775 at 1/30 dilution (2µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab313775 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse heart tissue lysate 5 µg
Lane 2 : ab313775 IP in Mouse heart tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab313775 in mouse heart tissue lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 3 seconds The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 27302065).
All lanes:
Immunoprecipitation - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] (<a href='/en-us/products/primary-antibodies/glucose-transporter-glut4-antibody-epr26571-45-ab313775'>ab313775</a>) at 1/30 dilution
All lanes:
Mouse heart tissue lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 3s
- WB
Supplier Data
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Negative control : liver (PMID : 2654938). Samples are non-boiled as boiling may cause protein aggregation. In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution. Exposure time : 48 seconds
All lanes:
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] (<a href='/en-us/products/primary-antibodies/glucose-transporter-glut4-antibody-epr26571-45-ab313775'>ab313775</a>) at 1/1000 dilution
Lane 1:
Human skeletal muscle tissue lysate at 20 µg
Lane 2:
Human liver tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/1000 dilution
Observed band size: 51 kDa
false
Exposure time: 48s
- WB
Supplier Data
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This blot was developed using a high sensitivity ECL substrate. The high-sensitivity ECL substrate used allows for the detection of proteins in the mid-femtogram range.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] (<a href='/en-us/products/primary-antibodies/glucose-transporter-glut4-antibody-epr26571-45-ab313775'>ab313775</a>) at 1/1000 dilution
Lane 1:
RD (Human muscle rhabdomyosarcoma) whole cell lysate at 20 µg
Lane 2:
A673 (human muscle Ewing's Sarcoma) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 51 kDa
true
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Low expression : kidney (PMID : 2654938). Samples are non-boiled as boiling may cause protein aggregation. In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution. Exposure time : 105 seconds
All lanes:
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] (<a href='/en-us/products/primary-antibodies/glucose-transporter-glut4-antibody-epr26571-45-ab313775'>ab313775</a>) at 1/1000 dilution
Lane 1:
Mouse skeletal muscle tissue lysate at 20 µg
Lane 2:
Mouse heart tissue lysate at 20 µg
Lane 3:
Mouse kidney tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 51 kDa
false
Exposure time: 105s
- WB
Supplier Data
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This blot was developed using a high sensitivity ECL substrate. The high-sensitivity ECL substrate used allows for the detection of proteins in the mid-femtogram range.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] (<a href='/en-us/products/primary-antibodies/glucose-transporter-glut4-antibody-epr26571-45-ab313775'>ab313775</a>) at 1/1000 dilution
Lane 1:
Untreated 3T3-L1 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 2:
3T3-L1 differentiation for 6 days whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 51 kDa
true
Exposure time: 158s
- WB
Supplier Data
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Negative control : liver (PMID : 2654938), lung (PMID : 2654938). Samples are non-boiled as boiling may cause protein aggregation. In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution. Exposure time : 15 seconds
All lanes:
Western blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] (<a href='/en-us/products/primary-antibodies/glucose-transporter-glut4-antibody-epr26571-45-ab313775'>ab313775</a>) at 1/1000 dilution
Lane 1:
Rat heart tissue lysate at 20 µg
Lane 2:
Rat liver tissue lysate at 20 µg
Lane 3:
Rat lung tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 51 kDa
false
Exposure time: 15s
- Dot
Supplier Data
Dot Blot - Anti-Glucose Transporter GLUT4 antibody [EPR26571-45] - BSA and Azide free (AB313776)
This data was developed using ab313775, the same antibody clone in a different buffer formulation. Dot blot analysis of SLC2A4 using ab313775 at 1 : 1000 (0.518 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution. Exposure time : 8 seconds. Blocking and diluting buffer and concentration : 5% NFDM/TBST
Related conjugates and formulations (1)
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Anti-Glucose Transporter GLUT4 antibody [EPR26571-45]
Reactivity data
Product details
ab313776 is the carrier-free version of ab313775.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
GLUT4 helps regulate blood sugar levels through its control over glucose uptake in muscle and adipose tissues. As an important component of the insulin-regulated glucose transport system GLUT4 responds to increased insulin levels by moving to the cell's surface aiding in glucose transportation into the cell. This adaptive response reduces blood glucose concentration after food intake. GLUT4 operates largely independently but may interact with other glucose transporters like GLUT1 to maintain normal cellular glucose homeostasis.
Pathways
GLUT4 plays a significant role in the insulin signaling pathway and glucose homeostasis. Activation of the insulin receptor triggers a signaling cascade that includes enzymes like Akt (protein kinase B) which facilitates the translocation of GLUT4 vesicles to the plasma membrane. This translocation is important for glucose entry into the cells. Other key proteins in this pathway include IRS (insulin receptor substrate) proteins which act as signaling intermediates to link insulin receptor activation to downstream targets like GLUT4. Its activity is central to the maintenance of energy balance and storage in the body.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com