catalog number :
MBS7233681
products type :
ELISA Kit
products full name :
Human beta sarcoglycan (SGCB) ELISA Kit
products short name :
[beta sarcoglycan (SGCB)]
products name syn :
[Human b sarcoglycan (SGCB) ELISA Kit]
other names :
[beta-sarcoglycan; Beta-sarcoglycan; beta-sarcoglycan; 43DAG; beta-SG; 43 kDa dystrophin-associated glycoprotein; limb girdle muscular dystrophy 2E (non-linked families); beta-sarcoglycan(43kD dystrophin-associated glycoprotein); sarcoglycan, beta (43kDa dystrophin-associated glycoprotein); 43 kDa dystrophin-associated glycoprotein; 43DAG; A3b]
products gene name :
[SGCB]
products gene name syn :
[SGCB]
other gene names :
[SGCB; SGCB; A3b; SGC; LGMD2E; Beta-SG; 43DAG]
uniprot entry name :
SGCB_HUMAN
storage stability :
Store all reagents at 2-8 degree C.
other info1 :
Samples: Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate. Assay Type: Competitive. Detection Range: 0.5-10ng/mL. Sensitivity: 0.1ng/mL
products categories :
Signal Transduction
ncbi acc num :
NP_000223.1
ncbi gb acc num :
NM_000232.4
ncbi mol weight :
34,777 Da
ncbi pathways :
Arrhythmogenic Right Ventricular Cardiomyopathy Pathway (672454); Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Pathway (117293); Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Pathway (116129); Dilated Cardiomyopathy Pathway (121494); Dilated Cardiomyopathy Pathway (121285); Hypertrophic Cardiomyopathy (HCM) Pathway (114229); Hypertrophic Cardiomyopathy (HCM) Pathway (106591); Viral Myocarditis Pathway (125138)
ncbi summary :
This gene encodes a member of the sarcoglycan family. Sarcoglycans are transmembrane components in the dystrophin-glycoprotein complex which help stabilize the muscle fiber membranes and link the muscle cytoskeleton to the extracellular matrix. Mutations in this gene have been associated with limb-girdle muscular dystrophy.[provided by RefSeq, Oct 2008]
uniprot summary :
SGCB: 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. Defects in SGCB are the cause of limb-girdle muscular dystrophy type 2E (LGMD2E). LGMD2E is an autosomal recessive disorder. Belongs to the sarcoglycan beta/delta/gamma/zeta family. Protein type: Dystrophin complex; Membrane protein, integral. Chromosomal Location of Human Ortholog: 4q12. Cellular Component: dystrophin-associated glycoprotein complex; cytoskeleton; integral to plasma membrane; cytoplasm; sarcoglycan complex; sarcolemma. Biological Process: muscle development; cardiac muscle cell development; muscle fiber development. Disease: Muscular Dystrophy, Limb-girdle, Type 2e
size4 :
10x96-Strip-Wells