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Fig. 7 The comparison of sample with standard sample.
High molecular weight genomic DNA was extracted from whole blood sample with standard salting out methods.
Transfer, gelatinize, and titrate the sample with standard 0.10 N sodium hydroxide in the same manner as the demineralized sample.
○ Bar graph of relative 5hmC intensity for each sample with standard deviations (as in Figure 8A, right).
Ester identification and quantification were done by comparing the retention time and peak area of the sample with standard.
C-reactive protein (CRP) was determined by using a highly sensitive latex particle-enhanced immunoturbidimetric assay that compares the laboratory sample with standard CRP dilutions.
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Phenolic compounds were identified according to their retention times as well as by spiking the sample with standards.
These compounds have been identified according to their retention time and the spectral characteristics of their peaks compared to those of standards as well as by spiking the sample with standards.
Quantification had to be performed using standard addition, since the slope of the calibration curve in pure water was different from the one obtained by spiking the fermentation sample with standards.
Recovery experiments were performed using spiked honey samples with standard deviation values from 0.75% and 9.69%.
The accuracy of the PPMS specific-heat data is determined here by comparing data measured on copper and synthetic sapphire samples with standard literature values.
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