"Sgca" Related Products

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Recombinant Mouse Sgca, His-tagged

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

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