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The schematic mechanism of dye assay's absorption and desorption is shown in Figure 7.
We also successfully amplified 92.5% of market samples, demonstrating the assay's robustness.
Testing of the assay's reproducibility was repeated several times, and the same results were achieved.
Yields obtained in accuracy test for two concentration levels varied between 90 and 105%, confirming the assay's reliability.
The assay's specificity was confirmed by testing 10 isolates of MAP and 59 isolates of other bacterial species.
The assay's excellent specificity was also demonstrated using 17 standard (control) strains and 124 other bacterial strains cultured from drowning and non-drowning victims in our previous studies.
The assay's development will allow high-throughput screening of other thermostable glucose-producing enzymes, including those applicable to commercial biomass conversion.
We report distinct changes in forces measured from PCMs treated with exogenous aggrecan, illustrating the assay's potential to probe proteoglycan distribution.
We first consider the ideal situation of no classification errors, then the more realistic situation where marker assay's sensitivity, specificity and the rule of classification are imperfect.
Due to the PCR assay's excellent inclusivity, high sensitivity and specificity it may be used to detect the presence of Helicobacters.
In consequence, the assay's performance has become robust and predictable.
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