Anti-gamma Sarcoglycan Antibody [JA11-57]
ET1704-24
ApplicationsImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetSGCG
Overview
- SupplierHUABIO
- Product NameAnti-gamma Sarcoglycan Antibody [JA11-57]
- Delivery Days Customer7
- ApplicationsImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- Applications SupplierWB,IP,IHC-P
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDJA11-57
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID6445
- Target nameSGCG
- Target descriptionsarcoglycan gamma
- Target synonyms35DAG, A4, DAGA4, DMDA, DMDA1, LGMD2C, LGMDR5, MAM, SCARMD2, gamma-SG, gamma-sarcoglycan, 35 kDa dystrophin-associated glycoprotein, 35kD dystrophin-associated glycoprotein, sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
- HostRabbit
- IsotypeIgG
- Protein IDQ13326
- Protein NameGamma-sarcoglycan
- Scientific DescriptionThe sarcoglycan transmembrane proteins are members of the dystrophin complex. Sarcoglycans cluster together to form a complex, which is localized in the cell membrane of skeletal, cardiac and smooth muscle fibers. Four sarcoglycan subunit proteins, designated alpha-, beta-, gamma- and delta-sarcoglycan, form a complex on the skeletal muscle cell surface membrane. A genetic defect in any one of these proteins causes the loss or marked decrease of the whole sarcoglycan complex, which is observed in the autosomal recessive muscular dystrophy, sarcoglycanopathy. In smooth muscle, beta- and delta-sarcoglycans are associated with epsilon-sarcoglycan, a glycoprotein homologous to alpha-sarcoglycan. Additionally, a complete deficiency in delta-sarcoglycan is the cause of the Syrian hamster BIO.14 cardiomyopathy.
- ReactivityHuman
- Reactivity SupplierHuman
- Reactivity Supplier NoteMouse
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC41116161