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NDE1 Antikörper (AA 74-335)

Der Kaninchen Polyklonal anti-NDE1 Antikörper (ABIN7876714) detektiert spezifisch NDE1 in WB, ELISA, FACS und IHC (p). Dieser Antikörper reagiert spezifisch mit Proben aus Human.
Produktnummer ABIN7876714
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für NDE1 Antikörper (AA 74-335) (ABIN7876714)

Target

Alle NDE1 Antikörper anzeigen
NDE1

Reaktivität

  • 29
  • 5
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 26
  • 3
Kaninchen

Klonalität

  • 26
  • 3
Polyklonal

Konjugat

  • 19
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser NDE1 Antikörper ist unkonjugiert

Applikation

  • 18
  • 14
  • 10
  • 10
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Bindungsspezifität

    • 12
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 74-335

    Verwendungszweck

    NDE1 Antibody / NudE

    Aufreinigung

    Affinity purified

    Immunogen

    An E. coli-derived human protein (amino acids E74-C335) was used as the immunogen for the NDE1 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the NDE1 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    After reconstitution, the NDE1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    NDE1

    Andere Bezeichnung

    NDE1

    Hintergrund

    Nuclear distribution protein nudE homolog 1 is a protein that in humans is encoded by the NDE1 gene. 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 cognitive disability. Alternative splicing results in multiple transcript variants.

    UniProt

    Q9NXR1
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