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CCM2 anticorps

Cet anticorps anti-CCM2 est un anticorps Souris Monoclonal détectant CCM2 dans WB, IF et IHC. Adapté pour Humain.
N° du produit ABIN2725241

Aperçu rapide pour CCM2 anticorps (ABIN2725241)

Antigène

Voir toutes CCM2 Anticorps
CCM2 (Cerebral Cavernous Malformation 2 (CCM2))

Reactivité

  • 27
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 19
  • 7
  • 1
Souris

Clonalité

  • 23
  • 4
Monoclonal

Conjugué

  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CCM2 est non-conjugé

Application

  • 18
  • 6
  • 5
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)

Clone

2E4
  • Attributs du produit

    Homo sapiens cerebral cavernous malformation 2 (CCM2), transcript variant 2

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogène

    Full length human recombinant protein of human CCM2(NP_113631) produced in HEK293T cell.

    Isotype

    IgG1
  • Indications d'application

    WB 1:2000, IHC 1:150, IF 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

    CCM2 (Cerebral Cavernous Malformation 2 (CCM2))

    Autre désignation

    CCM2

    Sujet

    This gene encodes a scaffold protein that functions in the stress-activated p38 Mitogen-activated protein kinase (MAPK) signaling cascade. The protein interacts with SMAD specific E3 ubiquitin protein ligase 1 (also known as SMURF1) via a phosphotyrosine binding domain to promote RhoA degradation. The protein is required for normal cytoskeletal structure, cell-cell interactions, and lumen formation in endothelial cells. Mutations in this gene result in cerebral cavernous malformations. Multiple transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    48.7 kDa

    ID gène

    83605

    NCBI Accession

    NM_031443

    HGNC

    83605

    Pathways

    Cell-Cell Junction Organization
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