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PHF6 anticorps

PHF6 Reactivité: Humain, Souris ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7251841
  • Antigène Voir toutes PHF6 Anticorps
    PHF6 (PHD Finger Protein 6 (PHF6))
    Reactivité
    • 31
    • 6
    • 5
    • 5
    • 5
    • 5
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 29
    • 2
    Lapin
    Clonalité
    • 30
    • 1
    Polyclonal
    Conjugué
    • 21
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp PHF6 est non-conjugé
    Application
    • 20
    • 7
    • 6
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human PHF6
    Isotype
    IgG
    Top Product
    Discover our top product PHF6 Anticorps primaire
  • Indications d'application
    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
    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
    PHF6 (PHD Finger Protein 6 (PHF6))
    Autre désignation
    PHF6 (PHF6 Produits)
    Synonymes
    anticorps zgc:55403, anticorps wu:fa22g03, anticorps BFLS, anticorps BORJ, anticorps CENP-31, anticorps 2700007B13Rik, anticorps 4931428F02Rik, anticorps mKIAA1823, anticorps PHD finger protein 6, anticorps PHD finger protein 6 L homeolog, anticorps phf6, anticorps phf6.L, anticorps PHF6, anticorps Phf6
    Sujet
    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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