DTNA anticorps (AA 240-480)

N° du produit ABIN6139849

Détail du produit anti-DTNA anticorps

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Épitope: AA 240-480

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DTNA est non-conjugé

Application: Western Blotting (WB)

Séquence: PVECSYCHSE SMMGFRYRCQ QCHNYQLCQD CFWRGHAGGS HSNQHQMKEY TSWKSPAKKL TNALSKSLSC ASSREPLHPM FPDQPEKPLN LAHIVDTWPP RPVTSMNDTL FSHSVPSSGS PFITRSSPPK DSEVEQNKLL ARAAPAFLKG KGIQYSLNVA DRLADEHVLI GLYVNMLRNN PSCMLESSNR LDEEHRLIAR YAARLAAESS SSQPPQQRSA PDISFTIDAN KQQRQLIAEL E

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 240-480 of human DTNA (NP_001381.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur DTNA

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Autre désignation: DTNA (DTNA Produits)

Synonymes: anticorps adtn, anticorps atnb, anticorps MGC146484, anticorps 2210407P21Rik, anticorps A0, anticorps Dtn, anticorps a-DB-1, anticorps adbn, anticorps D18S892E, anticorps DRP3, anticorps DTN, anticorps DTN-A, anticorps LVNC1, anticorps Dtna-ps1, anticorps RGD1561985, anticorps dystrobrevin alpha, anticorps dystrobrevin, alpha, anticorps DTNA, anticorps dtna, anticorps LOC100195747, anticorps Dtna

Sujet: 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.,DTNA,D18S892E,DRP3,DTN,DTN-A,LVNC1,Signal Transduction,Cell Biology & Developmental Biology,Cell Adhesion,Tight Junctions,Cytoskeleton,Neuroscience,Cell Type Marker,Neuron marker,Synapse marker,DTNA

Poids moléculaire: 22 kDa/36 kDa/41-44 kDa/50 kDa/58-83 kDa

ID gène: 1837

UniProt: Q9Y4J8