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Alginate Antikörper

Dieses Anti--Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von in ELISA. Geeignet für Pseudomonas.
Produktnummer ABIN7489925

Kurzübersicht für Alginate Antikörper (ABIN7489925)

Target

Alginate

Reaktivität

Pseudomonas

Wirt

  • 10
Maus

Klonalität

  • 10
Monoklonal

Konjugat

  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Unkonjugiert

Applikation

  • 10
  • 10
ELISA

Klon

3G4-1F5
  • Kreuzreaktivität

    Pseudomonas

    Immunogen

    Sodium alginate conjugated to KLH

    Isotyp

    IgG1
  • Applikationshinweise

    ELISA: Use at 0.5-20 μg/mL with alginate on the solid phase. Working concentrations for these antibodies are dependent on the purity and concentration of alginate in samples tested.

    Kommentare

    Anti-Alginate Mouse Monoclonal Antibody

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Rekonstitution

    Dilute in PBS or medium that is identical to that used in the assay system.

    Konzentration

    Lot specific

    Buffer

    50 % Glycerol,PBS, pH 7.4, 50 % glycerol, 0.1 % sodium azide.,Phosphate Buffered Saline

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    These antibodies are stable for at least one (1) year at -20°C. Store in appropriate aliquots to avoid multiple freeze-thaw cycles.
  • Target

    Alginate

    Substanzklasse

    Chemical

    Hintergrund

    Pulmonary infection by mucoid, alginate-producing Pseudomonas aeruginosa is the leading cause of mortality among patients suffering from cystic fibrosis. During early childhood, cystic fibrosis patients are colonized by multiple bacterial pathogens including nonmucoid P. aeruginosa. The appearance of mucoid isolates indicates progression to chronic infections. Recent evidence indicates that P. aeruginosa is most resistant to antibiotics when the infecting cells are present as a biofilm, as they appear to be in the lungs of cystic fibrosis patients.
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