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RECQL2 Antikörper (AA 122-240)

WRN Reaktivität: Human, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN4886768
  • Target Alle RECQL2 (WRN) Antikörper anzeigen
    RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))
    Bindungsspezifität
    • 7
    • 7
    • 7
    • 7
    • 7
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 122-240
    Reaktivität
    Human, Ratte
    Wirt
    • 34
    • 7
    Kaninchen
    Klonalität
    • 34
    • 7
    Polyklonal
    Konjugat
    • 24
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser RECQL2 Antikörper ist unkonjugiert
    Applikation
    • 31
    • 21
    • 13
    • 7
    • 6
    • 4
    • 4
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Verwendungszweck
    Rabbit IgG polyclonal antibody for Werner syndrome ATP-dependent helicase(WRN) detection. Tested with WB in Human,Rat.
    Kreuzreaktivität (Details)
    No cross reactivity with other proteins.
    Produktmerkmale
    Rabbit IgG polyclonal antibody for Werner syndrome ATP-dependent helicase(WRN) detection. Tested with WB in Human,Rat.
    Gene Name: Werner syndrome RecQ like helicase
    Protein Name: Werner syndrome ATP-dependent helicase
    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
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  • Applikationshinweise
    WB: Concentration: 0.1-0.5 μg/mL, Tested Species: Human, Rat
    Notes: Tested Species: Species with positive results.
    Other applications have not been tested. Optimal dilutions should be determined by end users.
    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
    At -20°C for one year. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20 °C for a longer time. Avoid repeated freezing and thawing.
  • Target
    RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))
    Andere Bezeichnung
    WRN (WRN Produkte)
    Synonyme
    RECQ3 antikoerper, RECQL2 antikoerper, RECQL3 antikoerper, xBLM antikoerper, recq2 antikoerper, recql2 antikoerper, recql3 antikoerper, AI846146 antikoerper, ffa-1 antikoerper, xwrn antikoerper, RGD1564788 antikoerper, Werner syndrome RecQ like helicase antikoerper, mediator of RNA polymerase II transcription subunit 34 antikoerper, Bloom syndrome RecQ like helicase antikoerper, Werner syndrome, RecQ helicase-like L homeolog antikoerper, WRN antikoerper, LOC9327212 antikoerper, blm antikoerper, Wrn antikoerper, wrn.L antikoerper
    Hintergrund
    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.

    Synonyms: Exonuclease WRN | RecQ3 | RECQL2 | RECQL3 | WRN | Q14191
    Gen-ID
    7486
    UniProt
    Q14191
    Pathways
    DNA Reparatur
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