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Relative qPCR measures the differences in abundances of the target DNA or RNA (reverse-transcribed to cDNA) between samples without showing their actual abundances, and the comparison can only be done for samples run within the same qPCR reaction.
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Aging simulation was done for samples tested using SFE and ITS.
No dilution was done for samples with EC <200 μS/cm.
Intensive parametric studies have been done for samples with various crack types, crack widths and water heads.
This has been done for samples with arrays of decreasing anisotropy, from rectangular arrays (two-fold symmetry) to square arrays (four-fold symmetry).
SAXS measurements were done for samples containing different concentrations of ZnS and the obtained scattering curves are given in Fig. 4a.
PCR was done for samples tested positive by microscopy and/or RDT.
Census method is done for sampling and study was conducted according to informed consent of intensive care unit nurses of Jahrom University of Medical Sciences in 1394.
At least three remeltings were done for sample homogenization.
The same was done for sampling dates occurring after the outcome interval.
Air sampling with Hopcalite absorbent tubes and sampling pumps can be done for clearance sampling after a cleanup has been performed, but they require laboratory analysis.
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