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The first assay was realized by Hwang et al. (2004).
The first assay can be used on samples containing mostly parasite DNA, like those prepared from infected erythrocytes.
Specimens were chosen on the basis of having fallen within the linear range of the first assay.
The first assay included primers and probes for 'Candidatus Liberibacter asiaticus' (CLas) and Citrus tristeza virus (CTV) broad spectrum detection and genotype differentiation (VT- and T3-like genotypes).
This is the first assay to allow the quantitation of NQO1 in live cells which can then be retained for further experiments.
In the first assay, a commonly used design was followed, in which the aptamer and target were incubated to allow binding followed by exposure to the AuNPs.
In the first assay, cell subsets were identified using fluorescently labeled antibodies, and viability was determined by staining with 50 μg/mL of propidium iodide (PI) to monitor losses in cell membrane integrity.
To our knowledge, this is the first assay designed for the simultaneous detection and genotyping of WNV by rapid, sensitive real-time PCR which may be implemented in diagnostic and epidemiology laboratories.
This assay is the first assay developed on single-step platform for nucleic acid detection of HBV and HCV with an extra edge over all other assays by providing inbuilt check for quality of sample.
The first assay obtained analyte measurements for 89 cytokines, the second for 90 cytokines.
This is our first assay using the primers to detect multiple blood meals from vectors.
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