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DTNB encodes dystrobrevin beta, a component of the dystrophin-associated protein complex (DPC). Additionally we are shipping Dystrobrevin beta Antibodies (68) and Dystrobrevin beta Kits (5) and many more products for this protein.
Showing 6 out of 7 products:
Data provide new insights into the role of beta-dystrobrevin in the molecular mechanisms underlying neuronal differentiation that could be relevant in the establishment of the cognitive impairment in Duchene muscular dystrophy.
beta-dystrobrevin interacts with the HMG20 (show UBC Proteins) proteins iBRAF (show HMG20A Proteins) and BRAF35 (show HMG20B Proteins)
results suggest that dysbindin (show DTNBP1 Proteins) assembled into BLOC-1 (show BLOC1S1 Proteins) is not a physiological binding partner of the dystrobrevins, likely due to engagement of its dystrobrevin (show DTNA Proteins)-binding region in interactions with other subunits
Dystrobrevin family gene expression in zebrafish is reported.
a novel function for dystrobrevin (show DTNA Proteins) as a motor protein receptor that might play a major role in the transport of components of the dystrophin (show DMD Proteins)-associated protein complex to specific sites in the cell
kinetics of the dystrobrevin-Kif5A interaction showed a lower affinity of alpha compared to that of beta-dystrobrevin for binding to kinesin
AlphaDB, betaDB, & dystrophin (show DMD Proteins) are concentrated at a discrete subset of inhibitory synapses on the somata & dendrites of cerebellar Purkinje cells. Sensorimotor behaviors reflecting cerebellar function are perturbed in mice lacking any of these proteins.
biglycan (show BGN Proteins) is important for the maintenance of muscle cell integrity and plays a direct role in regulating the expression and sarcolemmal localization of the intracellular signaling proteins dystrobrevin-1 and -2, alpha- and beta1-syntrophin (show SNTB1 Proteins) and nNOS (show NOS1 Proteins)
This gene encodes dystrobrevin beta, a component of the dystrophin-associated protein complex (DPC). The DPC consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and dystrobrevin alpha and beta. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Dystrobrevin beta is thought to interact with syntrophin and the DP71 short form of dystrophin. Alternatively spliced transcript variants encoding different isoforms have been identified.
, dystrobrevin beta
, dystrobrevin, beta
, dystrobrevin, gamma
, dystrobrevin beta-like
, myosin regulatory light chain 2, skeletal muscle isoform type 2
, fast skeletal myosin light chain 2
, Myosin regulatory light chain 2, skeletal muscle isoform type 1
, LOW QUALITY PROTEIN: dystrobrevin beta