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ENAH antibody (AA 485-589)

This anti-ENAH antibody is a Mouse Monoclonal antibody detecting ENAH in WB, ELISA and Coat. Suitable for Human.
Catalog No. ABIN6940390

Quick Overview for ENAH antibody (AA 485-589) (ABIN6940390)

Target

See all ENAH Antibodies
ENAH (Enabled Homolog (ENAH))

Reactivity

  • 50
  • 22
  • 20
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 37
  • 13
Mouse

Clonality

  • 37
  • 13
Monoclonal

Conjugate

  • 23
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ENAH antibody is un-conjugated

Application

  • 49
  • 15
  • 13
  • 6
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Coating (Coat)

Clone

ENAH-1988
  • Binding Specificity

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

    Purification

    Purified by Protein A/G

    Immunogen

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

    Isotype

    IgG2c kappa
  • Application Notes

    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.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-80 °C

    Storage Comment

    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.

    Expiry Date

    24 months
  • Target

    ENAH (Enabled Homolog (ENAH))

    Alternative Name

    ENAH

    Background

    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.

    Molecular Weight

    80/88/140kDa

    Gene ID

    55740

    UniProt

    Q8N8S7
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