Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

NDE1 Antikörper

NDE1 Reaktivität: Human, Maus, Ratte WB, IHC, ELISA, IF, IP Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5700144
  • Target Alle NDE1 Antikörper anzeigen
    NDE1
    Reaktivität
    • 14
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 11
    • 3
    Kaninchen
    Klonalität
    • 11
    • 3
    Polyklonal
    Konjugat
    • 14
    Dieser NDE1 Antikörper ist unkonjugiert
    Applikation
    • 12
    • 7
    • 4
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
    Immunogen
    nudE nuclear distribution gene E homolog 1 (A. nidulans)
    Isotyp
    IgG
    Top Product
    Discover our top product NDE1 Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Kommentare

    A2780 cells were subjected to SDS PAGE followed by western blot with FNab05600(NDE1 antibody) at dilution of 1:1500

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    PBS with 0.02 % sodium azide and 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.
    Handhabung
    Avoid repeated freeze / thaw cycles.
    Lagerung
    -20 °C
    Haltbarkeit
    12 months
  • Target
    NDE1
    Andere Bezeichnung
    NDE1 (NDE1 Produkte)
    Hintergrund
    Synonyms:NUDE Background: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.
    Molekulargewicht
    40 kDa
    Gen-ID
    54820
    UniProt
    Q9NXR1
Sie sind hier:
Kundenservice