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NDN anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-NDN a été validé pour WB et FACS. Il convient pour détecter NDN dans des échantillons de Humain.
N° du produit ABIN5537193

Aperçu rapide pour NDN anticorps (N-Term) (ABIN5537193)

Antigène

Voir toutes NDN Anticorps
NDN (Necdin Homolog (Mouse) (NDN))

Reactivité

  • 33
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 24
  • 9
Lapin

Clonalité

  • 25
  • 8
Polyclonal

Conjugué

  • 23
  • 3
  • 2
  • 2
  • 2
  • 1
Cet anticorp NDN est non-conjugé

Application

  • 26
  • 19
  • 10
  • 6
  • 6
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Épitope

    • 7
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 43-71, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This NDN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 43-71 amino acids from the N-terminal region of human NDN.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    For FACS starting dilution is: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène

    NDN (Necdin Homolog (Mouse) (NDN))

    Autre désignation

    NDN

    Sujet

    This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons.

    Poids moléculaire

    36 kDa

    ID gène

    4692

    UniProt

    Q99608

    Pathways

    Neurotrophin Signaling Pathway
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