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The binding energies for the samples were calibrated by setting the measured binding energy of C 1s to 284.60 eV.
The samples were calibrated in a thermocouple calibrating furnace in temperature range from 200 °C to 950 °C.
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The binding energies for the sample were calibrated by setting the measured binding energy of C1s to 284.60 eV.
Magnetic field values at the sample were calibrated with a DPPH (2,2-diphenyl-1-picrylhydrazyl) standard.
Finally, the irradiation power density on the surface of the sample was calibrated as 1000 W/m2.
To evaluate the photovoltaic performance, the irradiation power density on the surface of the sample was calibrated as set to 1000 W/m2.
Calibration coefficients in the synthetic samples were calibrated independently using standards prepared at the minimum, median, and maximum concentration of each metabolite in the synthetic mixtures (Table S-1 in Supporting Information).
Samples were calibrated with Peptide Calibration Standard (Bruker).
All samples were calibrated according to the expression of the EF1α gene that was analysed using primers 1818 and 1819.
Amplification results of affected samples were calibrated against those of controls to obtain the differences in gene expression.
In both techniques, samples were calibrated using data collected in a well-characterized methane/air diffusion flame supported on a Wolfhard-Parker slot burner.
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