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Eyes Absent Homolog 4 (EYA4) (Middle Region) Peptide

EYA4 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5512992
  • Antigène Tous les produits EYA4
    EYA4 (Eyes Absent Homolog 4 (EYA4))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 6
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    QESLPGLTNQ PGEFDTMQSP STPIKDLDER TCRSSGSKSR GRGRKNNPSP
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti- EYA4 Antibody. 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.
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    EYA4 (Eyes Absent Homolog 4 (EYA4))
    Synonymes
    B130023L16Rik Peptide, CMD1J Peptide, DFNA10 Peptide, EYA transcriptional coactivator and phosphatase 4 Peptide, Eya4 Peptide, EYA4 Peptide
    Sujet
    This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant non-syndromic sensorineural 10 locus. The encoded protein is also a putative oncogene that mediates DNA repair, apoptosis, and innate immunity following DNA damage, cellular damage, and viral attack. Defects in this gene are also associated with dilated cardiomyopathy 1J. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    Alias Symbols: CMD1J, DFNA10

    Protein Size: 585
    ID gène
    2070
    NCBI Accession
    NM_001301012, NP_004091
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