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Each sample was designated negative (0 ng/mL) or positive (>0 ng/mL) according to the LC/MSMS results.
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In addition, the non-neoplastic gastric tissue sample was designated as a calibrator for each paired tumor for clinicopathological analysis.
The relative quantification (RQ) of gene expression was calculated using the ΔΔCt method [ 19], in which the non-neoplastic sample was designated as a calibrator for each paired tumor sample.
This final sample was designated as V-Bi2S3.
CEM I (the control sample) was designated as C1, whereas blended cements were designated according to the replacement level.
Accordingly, 65% of our migrant sample was designated as "established migrants", with the balance subsequently referred to as "new migrants".
This sample was designated AH.EE.09.
A herd containing at least one positive serum sample was designated as seropositive.
The rabies virus from this sample was designated as H-1413-09.
In the present study, the corresponding normal tissue sample was designated as a calibrator for superficial gastritis, atrophic gastritis, or intestinal metaplasia sample from each patient.
Gene expression values were calculated based on the 2 −Delta Delta C TT)) method, where one sample was designated the calibrator, through which all other samples were analyzed [ 16].
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