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Ectodysplasin A (EDA) (Middle Region) Peptide

EDA Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN976122
  • Target See all Ectodysplasin A (EDA) products
    Ectodysplasin A (EDA)
    Protein Region
    Middle Region
    Origin
    Human
    Source
    • 6
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-EDA antibody (Catalog #: ARP44519_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    Ectodysplasin A (EDA)
    Synonyms
    ECTD1 Peptide, ED1 Peptide, ED1-A1 Peptide, ED1-A2 Peptide, EDA-A1 Peptide, EDA-A2 Peptide, EDA1 Peptide, EDA2 Peptide, HED Peptide, HED1 Peptide, ODT1 Peptide, STHAGX1 Peptide, XHED Peptide, XLHED Peptide, si:ch73-223d24.5 Peptide, Ed1 Peptide, Eda-A1 Peptide, Eda-A2 Peptide, Ta Peptide, tabby Peptide, RGD1563178 Peptide, ectodysplasin A Peptide, ectodysplasin-A Peptide, EDA Peptide, eda Peptide, Eda Peptide
    Background
    EDA is a type II membrane protein that can be cleaved by furin to produce a secreted form. It 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. 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.

    Alias Symbols: ED1, ED1-A1, ED1-A2, EDA1, EDA2, HED, XHED, XLHED, ODT1, STHAGX1

    Protein Interaction Partner: EDA,EDA2R,EDAR,FURIN,EDAR

    Protein Size: 389
    Molecular Weight
    41 kDa
    Gene ID
    1896
    NCBI Accession
    NM_001005609, NP_001005609
    UniProt
    B7ZLU4
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