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Recombinant Ectodysplasin A antibody (PE)

The Rabbit Chimeric anti-Ectodysplasin A antibody is suitable to detect Ectodysplasin A in samples from Human. It has been validated for FACS.
Catalog No. ABIN7867239
$927.69
Plus shipping costs $50.00
100 tests
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Recombinant Ectodysplasin A antibody (PE) (ABIN7867239)

Target

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

Antibody Type

Recombinant Antibody

Reactivity

  • 76
  • 56
  • 29
  • 10
  • 7
  • 7
  • 7
  • 7
  • 6
  • 6
  • 4
  • 3
  • 3
  • 2
  • 1
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  • 1
Human

Host

  • 69
  • 9
  • 2
Rabbit

Clonality

  • 67
  • 9
  • 2
Chimeric

Conjugate

  • 32
  • 5
  • 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 PE

Application

  • 64
  • 36
  • 26
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  • 23
  • 12
  • 10
  • 6
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  • 3
  • 2
  • 1
Flow Cytometry (FACS)

Clone

DMC388
  • Purpose

    PE-conjugated 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

    Liquid

    Buffer

    Liquid PBS with 0.05 %  Proclin300, 1 % BSA

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    4 °C

    Storage Comment

    Store at 2°C-8°C for 6 months

    Expiry Date

    6 months
  • Target

    Ectodysplasin A (EDA)

    Alternative Name

    EDA

    Background

    Synonyms: ED1, EDA2

    Target 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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