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The fluorescence intensity corresponding to hybridized cDNA sample is expressed as IS = [SB'] and the channel corresponding to the hybridized genomic DNA reference as IR = [RB'] + [R'B].
For the frame k, the n th baseband signal sample is expressed as begin{array}rcl@ x_{k}(n)=left{ begin{array}{ll} w_{k}(n), & z_{k}=0 s_{k}(n)+w_{k}(n), & z_{k}=1 end{array} right.
Parasite growth for each sample is expressed relative to plate PBS controls.
In this case, the signal intensity of each SNP in the target sample is expressed as a ratio over that of the normal sample or reference pool.
For the calibrator sample, the equation is relative quantity = 2−0, which is 1; therefore, every other sample is expressed relative to this.
Cytotoxicity of each sample is expressed as ±IC50 value.
Similar(48)
Gene expression for each sample was expressed as threshold cycle (Ct), normalized to the reference gene β- actin (Δ Ct).
The expression level of HO-1 mRNA in a sample was expressed as arbitrary units, which were determined by the formula 1AU = (HO-1 mRNA/GAPDH mRNA) × 100.
The absorbance of the sample was expressed as absorbance value at 450 nm (n = 5 for each group).
The results of the sample were expressed on dry weight basis except for bulk density, pH and conductivity.
Data from two replicate experiments and three repetitions of the analysis for each sample were expressed as the mean ± standard deviation (± SD).
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