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NDE1 antibody (AA 1-110)

This anti-NDE1 antibody is a Rabbit Polyclonal antibody detecting NDE1 in WB and IHC. Suitable for Human.
Catalog No. ABIN6144443

Quick Overview for NDE1 antibody (AA 1-110) (ABIN6144443)

Target

See all NDE1 Antibodies
NDE1

Reactivity

  • 16
  • 5
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 13
  • 3
Rabbit

Clonality

  • 13
  • 3
Polyclonal

Conjugate

  • 16
This NDE1 antibody is un-conjugated

Application

  • 14
  • 10
  • 6
  • 5
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-110

    Sequence

    MEDSGKTFSS EEEEANYWKD LAMTYKQRAE NTQEELREFQ EGSREYEAEL ETQLQQIETR NRDLLSENNR LRMELETIKE KFEVQHSEGY RQISALEDDL AQTKAIKDQL

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human NDE1 (NP_060138.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,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.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    NDE1

    Alternative Name

    NDE1

    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.,NDE1,HOM-TES-87,LIS4,MHAC,NDE,NUDE,NUDE1,Epigenetics & Nuclear Signaling,Cell Biology & Developmental Biology,Cell Cycle,Centrosome,Neuroscience,NDE1

    Molecular Weight

    37 kDa/38 kDa

    Gene ID

    54820

    UniProt

    Q9NXR1
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