Recombinant Mouse Sgca, His-tagged

• Cat.No.: Sgca-3387M
• Product Overview: Alpha-sarcoglycan (Sgca)

Specification

• Description: This gene encodes a member of the sarcoglycan alpha/epsilon family of transmembrane proteins. The encoded protein is part of the dystrophin-glycoprotein complex which links the extracellular matrix to the cytoskeleton in muscle fibers. Disruption of this gene results in progressive muscular dystrophy and is associated with the development of embryonal rhabdomysarcoma.
• Source: E. Coli or Yeast
• Species: Mouse
• Tag: His
• Form: This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications.
• Protein length: 387
• Purity: >90%
• Notes: Small volumes of Sgca recombinant protein may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice.
• Storage: Store at -20 degree C. For extended storage, store at -20 or -80 degree C.
• Storage Buffer: PBS pH 7.4, 50% glycerol
• Warning: This product is for research use only. Not for use in diagnostic or therapeutic procedures.

Gene Information

• Gene Name: Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) [ Mus musculus ]
• Official Symbol: Sgca
• Synonyms: SGCA; sarcoglycan, alpha (dystrophin-associated glycoprotein); alpha-sarcoglycan; alpha-SG; 50 kDa dystrophin-associated glycoprotein; sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein); Asg; 50DAG; 59kDa; adhalin
• Gene ID: 20391
• mRNA Refseq: NM_001136080
• Protein Refseq: NP_001129552
• Pathway: Arrhythmogenic right ventricular cardiomyopathy (ARVC), organism-specific biosystem; Arrhythmogenic right ventricular cardiomyopathy (ARVC), conserved biosystem; Dilated cardiomyopathy, organism-specific biosystem; Dilated cardiomyopathy, conserved biosys
• Function: calcium ion binding