Full length protein
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
Constituents: 0.3% Glutathione, 0.79% Tris HCl
- 35 kDa dystrophin associated glycoprotein
- 35 kDa dystrophin-associated glycoprotein
Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix.
Expressed in skeletal and heart muscle.
Defects in SGCG are the cause of limb-girdle muscular dystrophy type 2C (LGMD2C) [MIM:253700]. LGMD2C is characterized by progressive muscle wasting from early childhood.
Belongs to the sarcoglycan beta/delta/gamma/zeta family.
Cell membrane > sarcolemma. Cytoplasm > cytoskeleton.
Information by UniProt
has not yet been referenced specifically in any publications.
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