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RECQL2 anticorps

Cet anticorps anti-RECQL2 Polyclonal Lapin (ABIN7254655) détecte spécifiquement RECQL2 dans ELISA et IHC. L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN7254655
449,00 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 9 à 13 jours ouvrables

Aperçu rapide pour RECQL2 anticorps (ABIN7254655)

Antigène

Voir toutes RECQL2 (WRN) Anticorps
RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))

Reactivité

  • 49
  • 2
  • 1
Humain

Hôte

  • 33
  • 17
Lapin

Clonalité

  • 31
  • 19
Polyclonal

Conjugué

  • 29
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp RECQL2 est non-conjugé

Application

  • 37
  • 19
  • 16
  • 13
  • 10
  • 9
  • 6
  • 3
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Synthetic peptide of human WRN

    Isotype

    IgG
  • Indications d'application

    IHC 1:30-1:150, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.8 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

    RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))

    Autre désignation

    WRN

    Sujet

    This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases. DNA helicases are involved in many aspects of DNA metabolism, including transcription, replication, recombination, and repair. This protein contains a nuclear localization signal in the C-terminus and shows a predominant nucleolar localization. It possesses an intrinsic 3' to 5' DNA helicase activity, and is also a 3' to 5' exonuclease. Based on interactions between this protein and Ku70/80 heterodimer in DNA end processing, this protein may be involved in the repair of double strand DNA breaks. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by premature aging.

    UniProt

    Q14191

    Pathways

    Réparation de l'ADN
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