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NDE1 antibody

This anti-NDE1 antibody is a Rabbit Polyclonal antibody detecting NDE1 in WB, IHC, ELISA, IF and IP. Suitable for Human, Mouse and Rat.
Catalog No. ABIN5700144

Quick Overview for NDE1 antibody (ABIN5700144)

Target

See all NDE1 Antibodies
NDE1

Reactivity

  • 16
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 13
  • 3
Rabbit

Clonality

  • 13
  • 3
Polyclonal

Conjugate

  • 16
This NDE1 antibody is un-conjugated

Application

  • 14
  • 9
  • 6
  • 4
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • Purpose

    NDE1 antibody

    Immunogen

    nudE nuclear distribution gene E homolog 1 (A. nidulans)

    Isotype

    IgG
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

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

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Storage Comment

    -20°C for 12 months

    Expiry Date

    12 months
  • Target

    NDE1

    Alternative Name

    NDE1

    Background

    Synonyms: Nuclear distribution protein nudE homolog 1 (NudE)|NDE1|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.

    Molecular Weight

    40 kDa

    Gene ID

    54820

    UniProt

    Q9NXR1
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