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RECQL2 anticorps (AA 122-240)

L’anticorps Lapin Polyclonal anti-RECQL2 a été validé pour WB. Il convient pour détecter RECQL2 dans des échantillons de Humain et Rat.
N° du produit ABIN4886768

Aperçu rapide pour RECQL2 anticorps (AA 122-240) (ABIN4886768)

Antigène

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

Reactivité

Humain, Rat

Hôte

  • 31
  • 11
Lapin

Clonalité

  • 31
  • 11
Polyclonal

Conjugué

  • 25
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp RECQL2 est non-conjugé

Application

  • 32
  • 18
  • 14
  • 9
  • 8
  • 4
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 7
    • 6
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 122-240

    Fonction

    Anti-Werner's syndrome helicase WRN/WRN Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-Werner's syndrome helicase WRN/WRN Antibody Picoband® (ABIN4886768). Tested in WB applications. This antibody reacts with Human, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogène

    E. coli-derived human WRN recombinant protein (Position: Q122-N240). Human WRN shares 84% amino acid (aa) sequence identity with mouse WRN.

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.5 μg/mL, Human, Rat
    1. Ding SL, Shen CY (2008). "Model of human aging: recent findings on Werner's and Hutchinson-Gilford progeria syndromes". Clin Interv Aging3 (3): 431-44. 2. Rossi ML, Ghosh AK, Bohr VA (2010). "Roles of Werner syndrome protein in protection of genome integrity". DNA Repair (Amst.) 9 (3): 331-44.

    Commentaires

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg 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.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Antigène

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

    Autre désignation

    WRN

    Sujet

    Synonyms: Werner syndrome ATP-dependent helicase,3.6.4.12 ,DNA helicase, RecQ-like type 3,RecQ3,Exonuclease WRN,3.1.-.-,RecQ protein-like 2,WRN,RECQ3, RECQL2,

    Tissue Specificity: Widely expressed with higher expression in spleen, kidney and blood. Overexpressed in lesional psoriatic skin. .

    Background: Werner syndrome ATP-dependent helicase, also known as DNA helicase, RecQ-like type 3, is an enzyme that in humans is encoded by the WRN gene. 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.

    Poids moléculaire

    162 kDa, 200 kDa

    ID gène

    7486

    UniProt

    Q14191

    Pathways

    Réparation de l'ADN
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