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ENAH anticorps (AA 485-589)

Cet anticorps anti-ENAH est un anticorps Souris Monoclonal détectant ENAH dans WB, ELISA et Coat. Adapté pour Humain.
N° du produit ABIN6940390

Aperçu rapide pour ENAH anticorps (AA 485-589) (ABIN6940390)

Antigène

Voir toutes ENAH Anticorps
ENAH (Enabled Homolog (ENAH))

Reactivité

  • 51
  • 23
  • 21
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 37
  • 14
Souris

Clonalité

  • 37
  • 14
Monoclonal

Conjugué

  • 24
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ENAH est non-conjugé

Application

  • 50
  • 15
  • 13
  • 7
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Coating (Coat)

Clone

ENAH-1988
  • Épitope

    • 11
    • 8
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 485-589

    Purification

    Purified by Protein A/G

    Immunogène

    Recombinant fragment of human MENA protein (around aa 485-589) (exact sequence is proprietary)

    Isotype

    IgG2c kappa
  • Indications d'application

    Positive Control: MCF-7 cells. Uterus.

    Known Application: ELISA (For coating, order Ab without BSA),Western Blot (1-2 μg/mL)Optimal dilution for a specific application should be determined.

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    10 mM PBS with 0.05 % BSA & 0.05 % 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,-80 °C

    Stockage commentaire

    Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required.

    Date de péremption

    24 months
  • Antigène

    ENAH (Enabled Homolog (ENAH))

    Autre désignation

    ENAH

    Sujet

    The Wiskott-Aldrich syndrome (WAS) is characterized by thrombocytopenia, eczema, defects in cell-mediated and humoral immunity and a propensity for lymphoproliferative diseases. The syndrome is the result of a mutation in the gene encoding a proline-rich protein termed WASP. WASP is a downstream effector of Cdc42 and has been implicated in actin polymerization and cyto- skeletal organization. Distantly related proteins, VASP (vasodilator-stimulated phosphoprotein) and Mena (for mammalian enabled protein), are involved in the regulation of cytoskeletal dynamics. Both Mena and VASP accumulate at focal adhesions. Mena is highly expressed in the developing nervous system and may be involved in growth cone motility and axon guidance.

    Poids moléculaire

    80/88/140kDa

    ID gène

    55740

    UniProt

    Q8N8S7
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