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Dystrobrevin

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Involved in synapse maturation and required for normal muscle function.

Below are the list of possible Dystrobrevin products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Dystrobrevin alpha

 Dystrobrevin alpha ELISA Kit
 Dystrobrevin alpha Recombinant
 Dystrobrevin alpha Antibody
Also known as Dystrobrevin alpha (DTN-A) (Alpha-dystrobrevin).
DTNA: May be involved in the formation and stability of synapses as well as being involved in the clustering of nicotinic acetylcholine receptors. Defects in DTNA are the cause of left ventricular non- compaction type 1 (LVNC1). Left ventricular non- compaction is due to an arrest of myocardial morphogenesis. The disorder is charact
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erized by a hypertrophic left ventricle with deep trabeculations and with poor systolic function, with or without associated left ventricular dilation. In some cases, it is associated with other congenital heart anomalies such as ventricular septal defects, pulmonic stenosis and atrial septal defects. The right ventricle may also be affected. Belongs to the dystrophin family. Dystrobrevin subfamily. 10 isoforms of the human protein are produced by alternative splicing.

Protein type: Motility/polarity/chemotaxis

Cellular Component: axon; cell projection; cytoplasm; extrinsic to internal side of plasma membrane; protein complex; sarcolemma; synapse

Molecular Function: PDZ domain binding; protein binding
 Dtna ELISA Kit
 Dtna Recombinant
 Dtna Antibody
 Dtn ELISA Kit
 Dtn Recombinant
 Dtn Antibody
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Dystrobrevin beta

 Dystrobrevin beta ELISA Kit
 Dystrobrevin beta Recombinant
 Dystrobrevin beta Antibody
Also known as Dystrobrevin beta (DTN-B) (Beta-dystrobrevin).
DTNB: 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 var
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ious 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. [provided by RefSeq, Jul 2008]

Protein type: Calcium-binding; Motility/polarity/chemotaxis

Cellular Component: cytoplasm; synapse
 Dtnb ELISA Kit
 Dtnb Recombinant
 Dtnb Antibody
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Dystrobrevin-1

 Dystrobrevin-1 ELISA Kit
 Dystrobrevin-1 Recombinant
 Dystrobrevin-1 Antibody
Plays a role in cholinergic transmission and as a functional partner of dystrophin (dys-1), necessary for muscle maintenance.
 dyb-1 ELISA Kit
 dyb-1 Recombinant
 dyb-1 Antibody
 F47G6.1 ELISA Kit
 F47G6.1 Recombinant
 F47G6.1 Antibody
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