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Dityrosine Antikörper (HRP)

Dieses Anti-Dityrosine-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von Dityrosine in WB, ELISA, ICC und IF. Geeignet für .
Produktnummer ABIN5067464

Kurzübersicht für Dityrosine Antikörper (HRP) (ABIN5067464)

Target

Dityrosine (DT)

Wirt

  • 12
Maus

Klonalität

  • 12
Monoklonal

Konjugat

  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Dityrosine Antikörper ist konjugiert mit HRP

Applikation

  • 12
  • 11
  • 10
  • 10
  • 10
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (IF)

Klon

7D4
  • Spezifität

    Specific for dityrosine modified proteins. Does not cross-react with 3,5-dibromotyrosine or bromotyrosine modified proteins.

    Aufreinigung

    Protein G Purified

    Immunogen

    Synthetic Dityrosine conjugated to Keyhole Limpet Hemocyanin (KLH).

    Isotyp

    IgG1
  • Applikationshinweise

    • WB (1:1000)
    • ICC/IF (1:50)
    • ELISA (1:1000)
    • optimal dilutions for assays should be determined by the user.

    Kommentare

    A 1:1000 dilution of ABIN5067464 was sufficient for detection of dityrosine in 1 μg of Dityrosine conjugated to BSA by ECL immunoblot analysis using Goat Anti-Mouse IgG:HRP as the secondary Antibody.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    PBS pH 7.4, 50 % glycerol, 0.09 % Sodium azide, Storage buffer may change when conjugated

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    4 °C

    Informationen zur Lagerung

    Conjugated antibodies should be stored at 4°C
  • Target

    Dityrosine (DT)

    Andere Bezeichnung

    Dityrosine

    Substanzklasse

    Dipeptide

    Hintergrund

    ROS such as hydrogen peroxide (H2O2), superoxide, and hydroxyl radicals can react with both the backbone and the side chains of proteins, leading to backbone cleavage and side-chain modifications, respectively. Peroxidases, UV radiation, and hydroxyl radicals catalyze the formation of tyrosyl radicals which then react to form cross-links between proteins (1). This produces dityrosine, a metabolically stable biomarker of protein oxidation (2).
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