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BAZ1B Antikörper (N-Term)

BAZ1B Reaktivität: Human IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN965640
  • Target Alle BAZ1B Antikörper anzeigen
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    Bindungsspezifität
    • 15
    • 9
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    N-Term
    Reaktivität
    • 53
    • 14
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Wirt
    • 48
    • 5
    Kaninchen
    Klonalität
    • 41
    • 12
    Polyklonal
    Konjugat
    • 21
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser BAZ1B Antikörper ist unkonjugiert
    Applikation
    • 22
    • 16
    • 14
    • 13
    • 7
    • 5
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC)
    Aufreinigung
    Purified by antigen-specific affinity chromatography.
    Immunogen
    Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to N-terminal residues of human BAZ1B (bromodomain adjacent to zinc finger domain, 1B)
    Top Product
    Discover our top product BAZ1B Primärantikörper
  • Applikationshinweise
    ELISA, Western blotting: 1µg/ml for 2hrs.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    This antibody is stored in PBS, 50% glycerol
    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
  • Lu, Meng, Morris, Keating: "A novel human gene, WSTF, is deleted in Williams syndrome." in: Genomics, Vol. 54, Issue 2, pp. 241-9, (1999) (PubMed).

  • Target
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    Andere Bezeichnung
    BAZ1B (BAZ1B Produkte)
    Hintergrund
    The BAZ1B (bromodomain adjacent to zinc finger domain, 1B) is a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing of this gene generates at least 2 transcript variants.
    Pathways
    Nuclear Hormone Receptor Binding, Chromatin Binding
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