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RECQL2 Antikörper (AA 122-240)

Der Kaninchen Polyklonal Anti-RECQL2-Antikörper wurde für WB validiert. Er ist geeignet, RECQL2 in Proben von Human und Ratte zu detektieren.
Produktnummer ABIN4886768

Kurzübersicht für RECQL2 Antikörper (AA 122-240) (ABIN4886768)

Target

Alle RECQL2 (WRN) Antikörper anzeigen
RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))

Reaktivität

Human, Ratte

Wirt

  • 31
  • 11
Kaninchen

Klonalität

  • 31
  • 11
Polyklonal

Konjugat

  • 25
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser RECQL2 Antikörper ist unkonjugiert

Applikation

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

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

    Verwendungszweck

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

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    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.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

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

    Isotyp

    IgG
  • Applikationshinweise

    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.

    Kommentare

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Konzentration

    500 μg/mL

    Buffer

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

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Handhabung

    Avoid repeated freezing and thawing.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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.
  • Target

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

    Andere Bezeichnung

    WRN

    Hintergrund

    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.

    Molekulargewicht

    162 kDa, 200 kDa

    Gen-ID

    7486

    UniProt

    Q14191

    Pathways

    DNA Reparatur
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