Sentence examples for assays was calculated using from inspiring English sources

Standard deviation between triplicates in luciferase assays was calculated using Microsoft Excel 2010.

The percentage of growth inhibition for both MTT and SRB assays was calculated using the following formula: % cytotoxicity = A C - A B − A T − A B / A C − A B where AC, AT and AB is absorbance of control, test and blank, respectively.

qPCR reactions were run in duplicate and delta Cts for the splice assays were calculated using the Ct of the pre mRNA qPCR minus the Ct of the mRNA qPCR.

Differences in the distribution of women's characteristics for the three assays were calculated using the Χ distribution.

The cut-off values for the Bio-Rad TeSeE ELISA and Idexx assays were calculated using the mean of the absorbance values of 90 confirmed BSE negative brainstem samples+ 3 standard deviations.

The clinical sensitivity (true positive) and specificity (true negative) of the κ/ λ ratio of N Latex FLC and Freelite FLC assays were calculated using the outcomes of the IFE analysis.

The relative inhibition rate of the circle mycelium compared with the blank assay was calculated using the following equation.

The corrected fluorescence of the encoded microbeads before and during sandwich assay was calculated using ImageJ by the following formula: {text{Corrected}};{text{total}};{text{fluorescence}}, =,{text{Integrated}};{text{density}},, ( {text{Area}};{text{of}};{text{selected}};{text{beads}}, times,{text{Mean}};{text{fluorescence}};{text{of}};{text{background}};{text{readings)}} (1).

The sensitivity and specificity of the ALS assay was calculated using non-TB patients as controls.

The statistical significance of protein enrichment in c-ponatinib assay versus free ponatinib competition assay was calculated using the modification of the Decontaminator method.

From the concentration of DNA, the number of copies per assay was calculated using the 1C value (haploid genome mass in pg) derived from several references.