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NDE1 antibody (AA 74-335)

The Rabbit Polyclonal anti-NDE1 antibody (ABIN7876714) specifically detects NDE1 in WB, ELISA, IHC (p) and FACS. The antibody is reactive with Human samples.
Catalog No. ABIN7876714
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for NDE1 antibody (AA 74-335) (ABIN7876714)

Target

See all NDE1 Antibodies
NDE1

Reactivity

  • 18
  • 6
  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 15
  • 3
Rabbit

Clonality

  • 15
  • 3
Polyclonal

Conjugate

  • 18
This NDE1 antibody is un-conjugated

Application

  • 15
  • 11
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

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

    Purpose

    NDE1 Antibody / NudE

    Purification

    Affinity purified

    Immunogen

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

    Isotype

    IgG
  • Application Notes

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

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

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

    Storage

    4 °C,-20 °C

    Storage Comment

    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

    Alternative Name

    NDE1

    Background

    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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