Anti-TUG

Evaluated by Western Blotting in NIH3T3/L1 cell lysate.

Western Blotting Analysis: A 1:1,000 dilution of this antibody detected TUG in 10 µg of NIH3T3/L1 cell lysate.

Anti-TUG Antibody, Cat. No. ABN1664, is a highly specific rabbit polyclonal antibody that targets TUG and has been tested in Immunoprecipitation and Western blotting..

Research Category
Neuroscience

Western Blotting Analysis: A representative lot detected TUG in Western Blotting applications (Belman, J.P., et. al. (2015). J Biol Chem. 290(7):4447-63).

Immunoprecipitation Analysis: A representative lot detected TUG in Immunoprecipitation applications (Belman, J.P., et. al. (2015). J Biol Chem. 290(7):4447-63).

This polyclonal antibody detects TUG in NIH3T3/L1 cells. It targets an epitope within 29 amino acids from the N-terminal region.

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Tether containing UBX domain for GLUT4 (UniProt: Q8VBT9; also known as Alveolar soft part sarcoma chromosomal region candidate gene 1 protein homolog, TUG) is encoded by the Aspscr1 (also known as Tug) gene (Gene ID: 68938) in murine species. TUG is a 60-kDa protein present in the cytosol and on membranes. In the absence of insulin, it binds and sequesters GLUT4 intracellularly. Insulin stimulates the release of GLUT4 from TUG and facilitates GLUT4 translocation to cell membrane. TUG undergoes site-specific endoproteolytic cleavage, which separates a GLUT4-binding, N-terminal region of TUG from a C-terminal region. It has been shown that in 3T3-L1 cells, depletion of TUG can mobilize ~60-nm vesicles to the cell surface and these vesicles carry GLUT4 storage vesicle (GSV) cargoes and fuse with the plasma membrane. GSVs are distinct from other exocytic vesicles. It is shown that during exposure to insulin, GSV cargoes recycle in ~150-nm vesicles characteristic of endosomes and can bypass a TUG-regulated membrane trafficking step. Hence, GLUT4 can participate in two different exocytic pathways, which are active at distinct times after insulin addition in 3T3-L1 cells. It has been shown that TUG can link GLUT4 to Golgi matrix proteins, PIST and Golgin-160. Cleavage of TUG separates an N-terminal region that binds GLUT4 from a C-terminal region that binds Golgin-160 and this cleavage thus untethers GSVs from the Golgi matrix. (Ref.: Bogan, JS et al. (2012). J. Biol. Chem. 287(28); 23932 23947).

~59 kDa observed; 59.80 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

Epitope: N-terminus

KLH-conjugated linear peptide corresponding to 29 amino acids from the N-terminal region of murine Tether containing UBX domain for GLUT4 (TUG).

Concentration: Please refer to lot specific datasheet.

Rabbit polyclonal antiserum with 0.05% sodium azide.

Unpurified

Stable for 1 year at -20°C from date of receipt.

Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.