ARG58501

anti-DTNA / alpha dystrobrevin antibody

anti-DTNA / alpha dystrobrevin antibody for Western blot and Human,Mouse

Overview

Product Description Rabbit Polyclonal antibody recognizes DTNA / alpha dystrobrevin
Tested Reactivity Hu, Ms
Tested Application WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name DTNA / alpha dystrobrevin
Antigen Species Human
Immunogen Recombinant fusion protein corresponding to aa. 240-480 of Human DTNA / alpha dystrobrevin (NP_001381.2).
Conjugation Un-conjugated
Alternate Names D18S892E; DTN; DRP3; Dystrobrevin alpha; Alpha-dystrobrevin; LVNC1; Dystrophin-related protein 3; DTN-A

Application Instructions

Application Suggestion
Tested Application Dilution
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Mouse brain
Observed Size ~ 80 kDa

Properties

Form Liquid
Purification Affinity purified.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 13527 Mouse DTNA

GeneID: 1837 Human DTNA

Swiss-port # Q9D2N4 Mouse Dystrobrevin alpha

Swiss-port # Q9Y4J8 Human Dystrobrevin alpha

Gene Symbol DTNA
Gene Full Name dystrobrevin, alpha
Background The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Function May be involved in the formation and stability of synapses as well as being involved in the clustering of nicotinic acetylcholine receptors. [UniProt]
Cellular Localization Cytoplasm, Cell junction, synapse, Cell membrane. [UniProt]
Calculated MW 84 kDa
PTM Phosphorylation of DTN-1 on tyrosine kinase substrate domain present in the C-terminus. [UniProt]

Images (1) Click the Picture to Zoom In

  • ARG58501 anti-DTNA / alpha dystrobrevin antibody WB image

    Western blot: 25 µg of Mouse brain lysate stained with ARG58501 anti-DTNA / alpha dystrobrevin antibody at 1:3000 dilution.