Sarcoglycan α rabbit pAb
Sarcoglycan alpha (SGCA) Homo sapiens This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008],
Product Specifications
Background
Product Name Alternative
SGCA; ADL; DAG2; Alpha-sarcoglycan; Alpha-SG; 50 kDa dystrophin-associated glycoprotein; 50DAG; Adhalin; Dystroglycan-2
UniProt
Q16586
Swiss Prot
Q16586
Reactivity
Human; Mouse
Immunogen
The antiserum was produced against synthesized peptide derived from human SGCA. AA range:161-210
Target
Sarcoglycan α
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC
Concentration
1 mg/ml
Dilution
WB 1:500-2000; IHC-p 1:50-300
Buffer
-20°C/1 year
Molecular Weight
43kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
43kD
Fragment
IgG
Subcellular Location
Cell membrane, sarcolemma ; Single-pass type I membrane protein . Cytoplasm, cytoskeleton .
Other Product Names
SGCA; ADL; DAG2; Alpha-sarcoglycan; Alpha-SG; 50 kDa dystrophin-associated glycoprotein; 50DAG; Adhalin; Dystroglycan-2
Gene ID (Human)
6442
Available Sizes
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items
