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STK32A Antikörper

STK32A Reaktivität: Human, Maus WB, ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7247471
  • Target Alle STK32A Antikörper anzeigen
    STK32A (serine/threonine Kinase 32A (STK32A))
    Reaktivität
    • 35
    • 28
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 45
    • 3
    Kaninchen
    Klonalität
    • 45
    • 3
    Polyklonal
    Konjugat
    • 21
    • 5
    • 4
    • 4
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser STK32A Antikörper ist unkonjugiert
    Applikation
    • 39
    • 30
    • 15
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Fusion protein of human STK32A
    Isotyp
    IgG
    Top Product
    Discover our top product STK32A Primärantikörper
  • Applikationshinweise
    WB 1:500-1:2000, IHC 1:100-1:200, ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.68 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
    STK32A (serine/threonine Kinase 32A (STK32A))
    Andere Bezeichnung
    STK32A (STK32A Produkte)
    Synonyme
    YANK1 antikoerper, A930015B13Rik antikoerper, serine/threonine kinase 32A antikoerper, STK32A antikoerper, Stk32a antikoerper
    Hintergrund
    STK32A (serine/threonine kinase 32A), also known as YANK1, is a 396 amino acid protein that belongs to the superfamily of serine/threonine protein kinases and exists as three isoforms. The gene encoding STK32A maps to human chromosome 5, which is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene.
    Molekulargewicht

    Observed_MW: Refer to figures

    Calculated_MW: 46 kDa

    UniProt
    Q8WU08
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