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WRNIP1 anticorps

Cet anticorps anti-WRNIP1 est un anticorps Lapin Polyclonal détectant WRNIP1 dans ELISA et IHC. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7004728

Aperçu rapide pour WRNIP1 anticorps (ABIN7004728)

Antigène

Voir toutes WRNIP1 Anticorps
WRNIP1 (Werner Helicase Interacting Protein 1 (WRNIP1))

Reactivité

  • 20
  • 6
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 19
  • 1
Lapin

Clonalité

  • 20
Polyclonal

Conjugué

  • 15
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp WRNIP1 est non-conjugé

Application

  • 19
  • 10
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Synthetic peptide of human WRNIP1

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:100, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.96 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    Stockage commentaire

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

    WRNIP1 (Werner Helicase Interacting Protein 1 (WRNIP1))

    Autre désignation

    WRNIP1

    Sujet

    Werner's syndrome is a rare autosomal recessive disorder characterized by accelerated aging that is caused by defects in the Werner syndrome ATP-dependent helicase gene (WRN). The protein encoded by this gene interacts with the exonuclease-containing N-terminal portion of the Werner protein. This protein has a ubiquitin-binding zinc-finger domain in the N-terminus, an ATPase domain, and two leucine zipper motifs in the C-terminus. It has sequence similarity to replication factor C family proteins and is conserved from E. coli to human. This protein likely accumulates at sites of DNA damage by interacting with polyubiquinated proteins and also binds to DNA polymerase delta and increases the initiation frequency of DNA polymerase delta-mediated DNA synthesis. This protein also interacts with nucleoporins at nuclear pore complexes. Two transcript variants encoding different isoforms have been isolated for this gene.

    UniProt

    Q96S55
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