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Ectodysplasin A (EDA) Peptide

EDA Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN939171
  • Target See all Ectodysplasin A (EDA) products
    Ectodysplasin A (EDA)
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 6
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    HLQGQGSAIQ VKNDLSGGVL NDWSRITMNP KVFKLHPRSG ELEVLVDGTY
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of EDA antibody,
    Alternative Names: Ectodysplasin A control peptide, Ectodysplasin A antibody Blocking Peptide, Anti-Ectodysplasin A Blocking Peptide, ED1 Blocking Peptide, ED1-A1 Blocking Peptide, ED1-A2 Blocking Peptide, EDA1 Blocking Peptide, EDA2 Blocking Peptide, HED Blocking Peptide, XHED Blocking Peptide, XLHED Blocking Peptide, EDA Blocking Peptide
  • Application Notes
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20 °C long term.
  • 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.
    Molecular Weight
    41 kDa
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