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PHF8 antibody

PHF8 Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7269263
  • Target See all PHF8 Antibodies
    PHF8 (PHD Finger Protein 8 (PHF8))
    Reactivity
    • 29
    • 11
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 29
    • 1
    Rabbit
    Clonality
    • 29
    • 1
    Monoclonal
    Conjugate
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PHF8 antibody is un-conjugated
    Application
    • 14
    • 6
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    PHF8 Rabbit mAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human PHF8
    Isotype
    IgG
  • Application Notes
    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.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    PHF8 (PHD Finger Protein 8 (PHF8))
    Alternative Name
    PHF8 (PHF8 Products)
    Synonyms
    9830141C09Rik antibody, mKIAA1111 antibody, JHDM1F antibody, MRXSSD antibody, ZNF422 antibody, RGD1561065 antibody, zPHF8 antibody, PHD finger protein 8 antibody, Phf8 antibody, PHF8 antibody, phf8 antibody
    Background
    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
    Molecular Weight
    140kDa
    Gene ID
    23133
    UniProt
    Q9UPP1
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