DTNA anticorps

N° du produit ABIN2719777

Détail du produit anti-DTNA anticorps

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp DTNA est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Attributs du produit: Homo sapiens dystrobrevin, alpha (DTNA), transcript variant 5

Purification: Purified from mouse ascites fluids by affinity chromatography

Immunogène: Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.

Clone: 1B11

Isotype: IgG2b

Information d'application

Indications d'application: WB 1:2000, IF 1:100, FLOW 1:100

Commentaires:

The concentration of the product may vary between diferrent lots.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

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

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.

Poids moléculaire: 58.7 kDa

ID gène: 1837

NCBI Accession: NM_032979

HGNC: 1837