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DTNA anticorps

L’anticorps Souris Monoclonal anti-DTNA a été validé pour WB et FACS. Il convient pour détecter DTNA dans des échantillons de Humain et Singe.
N° du produit ABIN2719781

Aperçu rapide pour DTNA anticorps (ABIN2719781)

Antigène

Voir toutes DTNA Anticorps
DTNA (Dystrobrevin alpha (DTNA))

Reactivité

  • 17
  • 13
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Singe

Hôte

  • 16
  • 7
Souris

Clonalité

  • 19
  • 4
Monoclonal

Conjugué

  • 18
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DTNA est non-conjugé

Application

  • 22
  • 14
  • 9
  • 8
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

2F9
  • 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.

    Isotype

    IgG2a
  • Indications d'application

    WB 1:500~2000, FLOW 1:100

    Commentaires

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • 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
  • 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

    58.7 kDa

    ID gène

    1837

    NCBI Accession

    NM_032979

    HGNC

    1837
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