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Ectodysplasin A antibody (Biotin)

This anti-Ectodysplasin A antibody is a Human Chimeric antibody detecting Ectodysplasin A in FACS. Suitable for Human.
Catalog No. ABIN7608189

Quick Overview for Ectodysplasin A antibody (Biotin) (ABIN7608189)

Target

See all Ectodysplasin A (EDA) Antibodies
Ectodysplasin A (EDA)

Reactivity

  • 71
  • 55
  • 29
  • 10
  • 7
  • 7
  • 7
  • 7
  • 6
  • 6
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 68
  • 6
Human, Rabbit

Clonality

  • 67
  • 6
  • 1
Chimeric

Conjugate

  • 29
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Ectodysplasin A antibody is conjugated to Biotin

Application

  • 64
  • 34
  • 26
  • 26
  • 20
  • 12
  • 10
  • 6
  • 5
  • 3
  • 1
  • 1
Flow Cytometry (FACS)

Clone

DMC388
  • Purpose

    Biotinylated Anti-EDA antibody(DMC388), IgG1 Chimeric mAb

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG1
  • Application Notes

    Flow Cyt 1:100

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    Storage

    -20 °C,-80 °C

    Storage Comment

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    Expiry Date

    12 months
  • Target

    Ectodysplasin A (EDA)

    Alternative Name

    EDA

    Background

    The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene.

    UniProt

    Q92838

    Pathways

    Tube Formation
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