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But in comparison with colorimetric and electrochemical assay, the performance is greatly improved.
While studies of patients with acetaminophen-induced liver injury can determine the sensitivity of the assay, the performance of the assay cannot be studied solely in this population.
TaqMan assay, the performance of a fully automated system based on the real-time PCR technology, was evaluated for nucleic acid extraction from plasma.
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For purposes of comparison, we also assayed the performance of SIFT and ANNOVAR for rare disease disease-gene identification Ng and Henikoff, 2006; Wang et al., 2010.
To this end, we embarked on a series of optimization and characterization experiments to assay the overall performance of the Access Array system in high-throughput methylation analysis.
We assayed the STM performance of the mGluR mutant dmGluRA 112b to independently confirm a function of mGluRs in olfactory learning (Bogdanik et al., 2004).
We evaluated in triplicate assays the performance of QM-MSP to quantify the methylation levels of NPY, PENK, and WIF1.
This EV RT-PCR assay exceeds the performance of the Roche AMPLICOR Enterovirus assay in a direct comparison.
In the performance assays, the cellulases were dosed at 20 mg total protein per gram of cellulose.
Therefore, this strain was selected as a reference to determine the parameters of our qPCR assay during the performance assessment.
For whole blood samples & the Vikia® HBsAg assay, the best performance was achieved for GIII (k = 79.75 %).
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