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The reproducibility of these assays is not extensively studied.
The CV% of these assays is generally well within 10%.
Therefore, the timeliness of integrating it as a detector in point-of-care assays is ideal.
Another consideration in assessing the sensitivity of the cell viability assays is MNP concentration.
The only potential limitation of antigen assays is their low sensitivity in patients with leukopenia [5].
The primary goal of transporter assays is to determine the kinetics of substrate transport.
For HBV infection, this window period with most serologic assays is 50 60 days.
The importance of these physicochemical characterization techniques and analytical assays is explained.
Overall, this set of RT-PCR assays is a powerful tool for enhanced influenza virus surveillance.
Agreement between vitamin E assays is essential to provide consistent result interpretation.
The development of rapid screening assays is essential for antiviral drug discovery.
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