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PHF6 Antikörper

PHF6 Reaktivität: Human, Maus ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7251841
  • Target Alle PHF6 Antikörper anzeigen
    PHF6 (PHD Finger Protein 6 (PHF6))
    Reaktivität
    • 31
    • 6
    • 5
    • 5
    • 5
    • 5
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 29
    • 2
    Kaninchen
    Klonalität
    • 30
    • 1
    Polyklonal
    Konjugat
    • 21
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser PHF6 Antikörper ist unkonjugiert
    Applikation
    • 20
    • 7
    • 6
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Fusion protein of human PHF6
    Isotyp
    IgG
    Top Product
    Discover our top product PHF6 Primärantikörper
  • Applikationshinweise
    IHC 1:100-1:300, ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.5 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    PHF6 (PHD Finger Protein 6 (PHF6))
    Andere Bezeichnung
    PHF6 (PHF6 Produkte)
    Synonyme
    zgc:55403 antikoerper, wu:fa22g03 antikoerper, BFLS antikoerper, BORJ antikoerper, CENP-31 antikoerper, 2700007B13Rik antikoerper, 4931428F02Rik antikoerper, mKIAA1823 antikoerper, PHD finger protein 6 antikoerper, PHD finger protein 6 L homeolog antikoerper, phf6 antikoerper, phf6.L antikoerper, PHF6 antikoerper, Phf6 antikoerper
    Hintergrund
    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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