Syntrophin alpha 1 Antibody (1E1) - BSA Free

Western Blot: Syntrophin alpha 1 Antibody (1E1) [NBP2-22587] - The cell lysates of HepG2 (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human SNTA1 antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.

• Reactivity: Hu
• Applications: WB, ELISA, ICC/IF
• Clone: 1E1
• Clonality: Monoclonal
• Host: Mouse
• Conjugate: Unconjugated
• Format: BSA Free
• Concentration: 1 mg/ml

Syntrophin alpha 1 Antibody (1E1) - BSA Free Summary

• Immunogen: Recombinant human Syntrophin alpha 1 (1-505aa) purified from E. coli
• Isotype: IgG2b Kappa
• Clonality: Monoclonal
• Host: Mouse
• Gene: SNTA1
• Purity: Protein A purified

Applications/Dilutions

• Dilutions:
  • ELISA 1:100-1:2000
  • Immunocytochemistry/ Immunofluorescence
  • Western Blot 1:1000

Packaging, Storage & Formulations

• Storage: Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
• Buffer: PBS (pH 7.4), 10% Glycerol
• Preservative: 0.02% Sodium Azide
• Concentration: 1 mg/ml
• Purity: Protein A purified

Alternate Names for Syntrophin alpha 1 Antibody (1E1) - BSA Free

• 59 kDa dystrophin-associated protein A1 acidic component 1
• dJ1187J4.5
• LQT12
• Pro-TGF-alpha cytoplasmic domain-interacting protein 1
• SNT1alpha-1-syntrophin
• syntrophin, alpha 1 (dystrophin-associated protein A1, 59kD, acidic component)
• syntrophin, alpha 1 (dystrophin-associated protein A1, 59kDa, acidic component)
• syntrophin-1
• TACIP1acidic alpha 1 syntrophin

Background

SNTA1 (Syntrophin alpha 1) is 505 amino acid protein. SNTA1 is adapter protein that binds to and probably organizes the subcellular localization of a variety of membrane proteins. It may link various receptors to the actin cytoskeleton and the extracellular matrix via the dystrophin glycoprotein complex. SNTA1 plays an important role in synapse formation and in the organization of UTRN and acetylcholine receptors at the neuromuscular synapse. Defects of SNTA1 are the cause of long QT syndrome type 12 (LQT12).

Limitations

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.

Bioinformatics

• Gene Symbol: SNTA1
• Uniprot:
  • NP_003089(Human)