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RNASEH2B Antikörper

Dieses Maus Monoklonal-Antikörper erkennt spezifisch RNASEH2B in WB, ICC und IF. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7467894

Kurzübersicht für RNASEH2B Antikörper (ABIN7467894)

Target

Alle RNASEH2B Antikörper anzeigen
RNASEH2B (Ribonuclease H2, Subunit B (RNASEH2B))

Reaktivität

  • 15
  • 1
  • 1
Human

Wirt

  • 14
  • 1
Maus

Klonalität

  • 14
  • 1
Monoklonal

Konjugat

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser RNASEH2B Antikörper ist unkonjugiert

Applikation

  • 15
  • 11
  • 7
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Klon

GT479
  • Kreuzreaktivität

    Human

    Aufreinigung

    Affinity purified by Protein G.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human RNaseH2B. The exact sequence is proprietary.

    Isotyp

    IgG1
  • Applikationshinweise

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    1XPBS pH 7, 20 % Glycerol, No Preservative

    Konservierungsmittel

    Without preservative

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    RNASEH2B (Ribonuclease H2, Subunit B (RNASEH2B))

    Andere Bezeichnung

    ribonuclease H2 subunit B

    Hintergrund

    Ribonuclease H2 subunit B , AGS2 , DLEU8,RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits (B and C) and specifically degrades the RNA of RNA:DNA hybrids. The protein encoded by this gene is the non-catalytic B subunit of RNase H2, which is thought to play a role in DNA replication. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Aicardi-Goutieres syndrome type 2 (AGS2). [provided by RefSeq]

    Molekulargewicht

    35 kDa

    Gen-ID

    79621

    UniProt

    Q5TBB1
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