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Alginate Antikörper

Reaktivität: Pseudomonas ELISA Wirt: Maus Monoclonal 3G4-1F5 unconjugated
Produktnummer 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
    Kreuzreaktivität
    Pseudomonas
    Immunogen
    Sodium alginate conjugated to KLH
    Klon
    3G4-1F5
    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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