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DOK7 anticorps

Cet anticorps Souris Monoclonal détecte spécifiquement DOK7 dans WB et FACS. Il présente une réactivité envers Humain.
N° du produit ABIN2719664

Aperçu rapide pour DOK7 anticorps (ABIN2719664)

Antigène

Voir toutes DOK7 Anticorps
DOK7 (Docking Protein 7 (DOK7))

Reactivité

  • 31
  • 22
  • 18
Humain

Hôte

  • 45
  • 4
  • 1
  • 1
Souris

Clonalité

  • 47
  • 4
Monoclonal

Conjugué

  • 20
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DOK7 est non-conjugé

Application

  • 40
  • 18
  • 13
  • 13
  • 10
  • 6
  • 6
  • 4
  • 4
  • 3
  • 2
Western Blotting (WB), Flow Cytometry (FACS)

Clone

3C12
  • Attributs du produit

    Homo sapiens docking protein 7 (DOK7), transcript variant 1

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogène

    Full length human recombinant protein of human DOK7(NP_775931) produced in HEK293T cell.

    Isotype

    IgG2b
  • Indications d'application

    WB 1:2000, 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

    DOK7 (Docking Protein 7 (DOK7))

    Autre désignation

    DOK7

    Sujet

    The protein encoded by this gene is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in this gene are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B. Alternative splicing results in multiple transcript variants.

    Poids moléculaire

    52.9 kDa

    ID gène

    285489

    NCBI Accession

    NM_173660

    HGNC

    285489

    Pathways

    Skeletal Muscle Fiber Development
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