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NDE1 Antikörper

NDE1 Reaktivität: Human, Maus, Ratte IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7011586
  • Target Alle NDE1 Antikörper anzeigen
    NDE1
    Reaktivität
    • 19
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 16
    • 3
    Kaninchen
    Klonalität
    • 16
    • 3
    Polyklonal
    Konjugat
    • 14
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser NDE1 Antikörper ist unkonjugiert
    Applikation
    • 17
    • 13
    • 4
    • 4
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human NDE1 (NP_060138.1).
    Isotyp
    IgG
    Top Product
    Discover our top product NDE1 Primärantikörper
  • Applikationshinweise
    IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    NDE1
    Andere Bezeichnung
    NDE1 (NDE1 Produkte)
    Synonyme
    2810027M15Rik antikoerper, AU042936 antikoerper, AW822251 antikoerper, Nude antikoerper, mNudE antikoerper, HOM-TES-87 antikoerper, LIS4 antikoerper, NDE antikoerper, NUDE antikoerper, NUDE1 antikoerper, fb82g01 antikoerper, im:7141877 antikoerper, wu:fb82g01 antikoerper, zgc:114109 antikoerper, nudE neurodevelopment protein 1 antikoerper, Nde1 antikoerper, NDE1 antikoerper, nde1 antikoerper
    Hintergrund
    This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe mental retardation. Alternative splicing results in multiple transcript variants.
    Gen-ID
    54820
    UniProt
    Q9NXR1
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