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Anti-Alginate, Pseudomonas-reactive, Antibody (15725)
Price
2,450.00 ₪
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.
Quantity
Storage and Stability
These antibodies are stable for at least one (1) year at -20°C. Store in appropriate aliquots to avoid multiple freeze-thaw cycles.
Formulation
PBS, pH 7.4, 50% glycerol, 0.1% sodium azide.
Shipping Conditions
Next Day 2-8°C
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