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A representative assay result is shown in Fig. 6A B.
In vitro assays were repeated three times (with equivalent results), in quadruplicate, and data presented (mean±standard error of the mean, SEM) are from a single representative assay.
A representative assay is shown in Figure 1 along with the nearly complete suppression of clotting obtained with the Staphylococcus epidermidis adhesin, SdrG [19], which has two- to threefold higher avidity for fibrinogen (data not shown).
Each assay was done twice, with one representative assay shown.
Means and the SD (bars) of two repeated measurements of a representative assay are shown.
A representative assay is presented (Fig. 2A), demonstrating that treatment with 160 produced a dose responsive reduction in luciferase activity.
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Furthermore, examples are provided where non-biologically representative assays are better at predicting protein and amino acid digestibility compared with those designed to mimic in vivo conditions.
Following the section of inhibitor design, we will briefly review representative assays that are available to evaluate the potency of these inhibitors along with a detailed description of the most commonly used radiometric assay.
2B and C show representative assays.
In each experiment, at least 50 cells were scored for each combination, and the results of representative assays are shown.
Data from representative assays are shown in Figure 4. Receptor protein (15 µg) was added to PA63 heptamer prepore (25 µg).
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