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WRN Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-53558

宿主: Rabbit

反应性: H

应用: IHC

  • 详情
  • Overview

    Synonyms DKFZp686C2056,DNA helicase,DNA helicase, RecQ like type 3,Exonuclease WRN,HGNC 12791,OTTHUMP00000225301,RecQ protein-like 2,RecQ-like type 3,RecQ3,RECQL2,RECQL3,Werner syndrome ATP-dependent helicase,Werner syndrome helicase,Werner syndrome protein,Werner syndrome, RecQ helicase like,WRN,WRN,WRN抗体
    Swissprot Q14191
    Source Rabbit
    Reactivity Human
    Immunogen Synthetic peptide of human WRN
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:30-1:150
    Concentration 0.8mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Nucleus>nucleolus. Nucleus.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
    Background 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.
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