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PHF6 antibody

PHF6 Reactivity: Human, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7251841
  • Target See all PHF6 Antibodies
    PHF6 (PHD Finger Protein 6 (PHF6))
    Reactivity
    • 34
    • 8
    • 7
    • 7
    • 6
    • 5
    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    Human, Mouse
    Host
    • 32
    • 2
    Rabbit
    Clonality
    • 33
    • 1
    Polyclonal
    Conjugate
    • 24
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PHF6 antibody is un-conjugated
    Application
    • 23
    • 7
    • 6
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human PHF6
    Isotype
    IgG
    Top Product
    Discover our top product PHF6 Primary Antibody
  • Application Notes
    IHC 1:100-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.5 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    PHF6 (PHD Finger Protein 6 (PHF6))
    Alternative Name
    PHF6 (PHF6 Products)
    Synonyms
    zgc:55403 antibody, wu:fa22g03 antibody, BFLS antibody, BORJ antibody, CENP-31 antibody, 2700007B13Rik antibody, 4931428F02Rik antibody, mKIAA1823 antibody, PHD finger protein 6 antibody, PHD finger protein 6 L homeolog antibody, phf6 antibody, phf6.L antibody, PHF6 antibody, Phf6 antibody
    Background
    This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms.
    UniProt
    Q8IWS0
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