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Human Polyclonal SGCB Primary Antibody für IHC, IHC (p) - ABIN4284180
Pozsgai, Griffin, Heller, Mendell, Rodino-Klapac: β-Sarcoglycan gene transfer decreases fibrosis and restores force in LGMD2E mice. in Gene therapy 2016
Show all 3 Pubmed References
This study demonstrated that LGMD2E is the most common type of sarcoglycanopathies in the Iranian population.
Clinical severity of limb-girdle muscular dystrophy type 2Emay be predicted by SGCB gene mutation and sarcoglycan (zeige SGCD Antikörper) protein expression.
Defective assembly of sarcoglycan (zeige SGCD Antikörper) complex in patients with beta-sarcoglycan gene mutations
beta-sarcoglycan and SPATA18 (zeige SPATA18 Antikörper) may have a role in limb-girdle muscular dystrophy type 2E
While the quantity of beta-sarcoglycan was nearly normal (zeige EEF1G Antikörper) in the limb girdle muscular dystrophy (LGMD)2E carrier, the levels of dysferlin (zeige DYSF Antikörper) protein were reduced to 50% of controls in the carriers of LGMD2B (zeige DYSF Antikörper).
These data suggest that formation of the beta-delta-core may promote the export and deposition of sarcoglycan (zeige SGCD Antikörper) subcomplexes at the plasma membrane, and therefore identifies a mechanism for sarcoglycan (zeige SGCD Antikörper) transport.
The limb-girdle muscular dystrophy patients with beta-sarcoglycan deficient LGMD2E do not enable an accurate prediction of the genotype.
Generate a new knock-in model carrying the missense mutation T151R in the beta-sarcoglycan gene since this is the second sarcoglycan (zeige SGCD Antikörper) protein with the most frequently reported missense mutations. Muscle analysis, performed at the age of 4 and 9-months, showed the presence of the mutated beta-sarcoglycan protein and of the other components of the dystrophin (zeige DMD Antikörper)-associated glycoprotein complex at the muscle membrane.
beta-Sarcoglycan deficiency reduces atherosclerotic plaque formation in ApoE (zeige APOE Antikörper)-knockout mouse model.
In Sgcb-null mice, severe morphological disruption was present from 4 weeks in both quadriceps and diaphragm, and included conspicuous deposition of extracellular matrix components.
Aging leads to changes in expression of beta-sarcoglycan in aged affected muscles (diaphragm and limb).
Sarcoglycan beta missense mutations affect sarcoglycan (zeige SGCD Antikörper) complex assembly and/or localization to the cell surface and provide information on the molecular mechanisms underlying the effects of various sarcoglycan (zeige SGCD Antikörper) mutations in muscular dystrophies.
Data demonstrate a novel function of the sarcoglycan (zeige SGCD Antikörper) complex in whole body glucose homeostasis and skeletal muscle metabolism, suggesting that the impairment of the skeletal muscle metabolism influences the pathogenesis of muscular dystrophy.
subcellular localization of dScgbeta dramatically changes during mitosis through possible association with tubulin (zeige TUBB Antikörper); these observations point to a complex role of sarcoglycans in non-muscle tissues.
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.
43 kDa dystrophin-associated glycoprotein
, beta-sarcoglycan(43kD dystrophin-associated glycoprotein)
, limb girdle muscular dystrophy 2E (non-linked families)
, sarcoglycan, beta (43kD dystrophin-associated glycoprotein)
, sarcoglycan beta
, SarcoGlycaN family member (sgn-1)