Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Western blot [3]
- Other assay [1]
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Validation data
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- Product number
- MA1-83191 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- GLUT4 Monoclonal Antibody (1F8)
- Antibody type
- Monoclonal
- Antigen
- Purifed from natural sources
- Description
- This antibody does not react with dog. This product requires enzyme-mediated antigen retrieval prior to staining of paraffin sections. Proteinase K is recommended. Mouse anti glucose transporter 4 antibody, clone 1F8 originally raised against rat intracellular low density microsomes (James et al.
- Reactivity
- Human, Mouse, Rat, Porcine, Rabbit
- Host
- Mouse
- Isotype
- IgG
- Antibody clone number
- 1F8
- Vial size
- 50 µg
- Concentration
- 1 mg/mL
- Storage
- Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Submitted references Cardiac contractility modulation ameliorates myocardial metabolic remodeling in a rabbit model of chronic heart failure through activation of AMPK and PPAR-α pathway.
Impaired HMG-CoA Reductase Activity Caused by Genetic Variants or Statin Exposure: Impact on Human Adipose Tissue, β-Cells and Metabolome.
Zhang F, Liu L, Xie Y, Wang J, Chen X, Zheng S, Li Y, Dang Y
Open medicine (Warsaw, Poland) 2022;17(1):365-374
Open medicine (Warsaw, Poland) 2022;17(1):365-374
Impaired HMG-CoA Reductase Activity Caused by Genetic Variants or Statin Exposure: Impact on Human Adipose Tissue, β-Cells and Metabolome.
Sarsenbayeva A, Jui BN, Fanni G, Barbosa P, Ahmed F, Kristófi R, Cen J, Chowdhury A, Skrtic S, Bergsten P, Fall T, Eriksson JW, Pereira MJ
Metabolites 2021 Aug 25;11(9)
Metabolites 2021 Aug 25;11(9)
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of 3T3-L1 lysate probed with a Glucose Transporter 4 monoclonal antibody (Product # MA1-83191) followed by Goat anti mouse IgG, Dylight 800 conjugate.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of 3T3-L1 lysate probed with a Glucose Transporter 4 monoclonal antibody (Product # MA1-83191)
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis was performed on membrane enriched extracts (30 µg lysate) of 3T3-L1 (Lane 1), 3T3-L1 differentiated to adipocytes (Lane 2), HeLa (Lane 3), Hep G2 (Lane 4), NIH/3T3 (Lane 5), C2C12 (Lane 6), tissue extracts of Mouse heart (Lane 7), Mouse Skin (Lane 8) and Mouse Skeletal Muscle (Lane 9). The blot was probed with Anti-GLUT4 Monoclonal Antibody (1F8) (Product # MA1-83191, 1:1000 dilution) and detected by chemiluminescence using Goat anti-Mouse IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate (Product # A28177, 0.25 µg/mL, 1:4000 dilution). A 53 kDa band corresponding to GLUT4 was observed across cell lines and tissue extracts tested and was also enhanced in 3T3-L1 after differentiating it to adipocytes. A 25 kDa band corresponding to free IgG was also observed in the tissue extracts.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 3 Effects of simvastatin and simvastatin acid on adipocyte differentiation. ( A ) Representative images of differentiation rate of adipocytes treated without (Control) or with Simvastatin 100 nM (Sim 100 nM), simvastatin hydroxy acid 8 and 30 nM (SA 8 nM and SA 30 nM, respectively). Left to right: Nuclei are shown in blue (DAPI), lipid droplets are shown in green (Bodipy), brightfield image, and merged. ( B ) Quantification of adipocyte differentiation rate. ( C ) The differentiation rate was also assessed by measuring the mRNA expression of the master regulator of adipogenesis PPARG . GUSB was used as the housekeeping gene. Relative gene expression was measured as 2 -DeltaDeltaCt . ( D ) Representative blot of GLUT4 expression in adipocytes treated without (Control) or with Simvastatin 100 nM (Sim 100 nM), simvastatin hydroxy acid 30 nM and 8.0 nM (SA 30 nM and SA 8 nM), respectively, at day 14. ( E ) Quantification of GLUT4 expression. Graphs show mean +- S.E.M. of n = 3 independent experiments.