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PHF8 anticorps

PHF8 Reactivité: Humain WB Hôte: Lapin Monoclonal unconjugated
N° du produit ABIN7269263
  • Antigène Voir toutes PHF8 Anticorps
    PHF8 (PHD Finger Protein 8 (PHF8))
    Reactivité
    • 29
    • 11
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 29
    • 1
    Lapin
    Clonalité
    • 29
    • 1
    Monoclonal
    Conjugué
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp PHF8 est non-conjugé
    Application
    • 14
    • 6
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Fonction
    PHF8 Rabbit mAb
     Réactivité croisée
    Humain, Souris, Rat
    Attributs du produit
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    A synthesized peptide derived from human PHF8
    Isotype
    IgG
  • Indications d'application
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    PHF8 (PHD Finger Protein 8 (PHF8))
    Autre désignation
    PHF8 (PHF8 Produits)
    Synonymes
    anticorps 9830141C09Rik, anticorps mKIAA1111, anticorps JHDM1F, anticorps MRXSSD, anticorps ZNF422, anticorps RGD1561065, anticorps zPHF8, anticorps PHD finger protein 8, anticorps Phf8, anticorps PHF8, anticorps phf8
    Sujet
    The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. Defects in this gene are a cause of mental retardation syndromic X-linked Siderius type (MRXSSD). Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010],JHDM1F, KDM7B, MRXSSD, ZNF422,Epigenetic writers and erasers of core Histones,Epigenetic writers and erasers of core Histones_Demethylation,Epigenetics & Nuclear Signaling,PHF8
    Poids moléculaire
    140kDa
    ID gène
    23133
    UniProt
    Q9UPP1
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