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CUL9 Antikörper (C-Term)

CUL9 Reaktivität: Human, Maus, Ratte WB, IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN356104
  • Target Alle CUL9 Antikörper anzeigen
    CUL9 (Cullin 9 (CUL9))
    Bindungsspezifität
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reaktivität
    • 18
    • 7
    • 2
    • 1
    Human, Maus, Ratte
    Wirt
    • 15
    • 4
    Kaninchen
    Klonalität
    • 15
    • 4
    Polyklonal
    Konjugat
    • 19
    Dieser CUL9 Antikörper ist unkonjugiert
    Applikation
    • 18
    • 9
    • 7
    • 6
    • 4
    • 4
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Kreuzreaktivität
    Human, Maus, Ratte (Rattus)
    Aufreinigung
    affinity purified
    Immunogen
    17 amino acid synthetic peptide from near the carboxy terminus of human PARC.
    Isotyp
    IgG
    Top Product
    Discover our top product CUL9 Primärantikörper
  • Applikationshinweise
    Optimal working dilutions should be determined experimentally by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Lagerung
    -20 °C
  • Target
    CUL9 (Cullin 9 (CUL9))
    Andere Bezeichnung
    PARC/P53-associated Parkin-like Cytoplasmic Protein (CUL9 Produkte)
    Synonyme
    H7AP1 antikoerper, PARC antikoerper, RP3-330M21.2 antikoerper, parc antikoerper, 1810035I07Rik antikoerper, Cul-9 antikoerper, Parc antikoerper, mKIAA0708 antikoerper, RGD1562008 antikoerper, cullin-9 antikoerper, cullin 9 antikoerper, cullin-9 antikoerper, CUL9 antikoerper, LOC100083225 antikoerper, cul9 antikoerper, LOC100561099 antikoerper, Cul9 antikoerper
    Hintergrund
    PARC (p53 associated parkin like cytoplasmic protein) antibody directly interacted and formed an approximately 1MD complex with p53 in the cytoplasm of unstressed cells. In the absence of stress, inactivation of PARC induced nuclear localization of endogenous p53 and activated p53 dependent apoptosis. Overexpression of PARC promoted cytoplasmic sequestration of ectopic p53. Furthermore, abnormal cytoplasmic localization of p53 was observed in a number of neuroblastoma cell lines, RNA interference-mediated reduction of endogenous PARC significantly sensitized these neuroblastoma cells in the DNA damage response. These results revealed that PARC is a critical regulator in controlling p53 subcellular localization and subsequent function.
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