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The highest performance of each phage is given by max(P).
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Here we analysed the impact of various factors on the performance of the phage display system.
The phage stability and in vitro aerosol performance of the phage powders were examined on the day of production and after 1, 3 and 12 months of storage.
For each network, let S be a vector containing the specificity of impacts of each phage and R a vector containing the specificity of associations.
To compare the relative numbers of phage hosts at each atoll, the incidence of each phage host genome per atoll was counted.
Single-residue alanine scanning mutagenesis of the CGRRAGGSC phage were produced and binding of each phage to immobilized IL-11Rα was tested in a functional assay (Table 2).
Genomic maps of each phage were prepared using Phamerator [ 62], an open-source program designed to compare phage genomes.
The supernatant of each phage clone was added to each microtiter well.
The clinical performance of this phage-based qPCR assay was evaluated with EDTA-treated human blood artificially contaminated with Y. pestis.
The performance of phage-derived materials as biorecognition interface was illustrated by detection of Bacillus anthracis spores and Salmonella typhimurium cells.
Differences in performance of phage-based tests compared to smear microscopy were also determined for smear-positive and smear-negative, culture-positive specimens.
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