DTNA anticorps (C-Term)

N° du produit ABIN656504

L’anticorps Lapin Polyclonal anti-DTNA a été validé pour WB, IF et IHC (p). Il convient pour détecter DTNA dans des échantillons de Humain et Souris.

Aperçu rapide pour DTNA anticorps (C-Term) (ABIN656504)

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DTNA est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB31275

Détail du produit anti-DTNA anticorps

Épitope: AA 692-721, C-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This DTNA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 692-721 amino acids from the C-terminal region of human DTNA.

Isotype: Ig Fraction

Information d'application

Indications d'application: IF: 1:10~50. WB: 1:2000. WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur DTNA

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Autre désignation: 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: 83901

ID gène: 1837

NCBI Accession: NP_001121647, NP_001185867, NP_001185868, NP_001185869, NP_001185871, NP_001185873, NP_001185874, NP_001381, NP_001382, NP_001383, NP_116757, NP_116760, NP_116761, NP_116762, NP_116763

UniProt: Q9Y4J8