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The performances of the onboard orbit determination were verified using real GPS data of the CHAMP and KOMPSAT-2 satellites.
Protein transfer efficiency and size determination were verified using prestained protein markers.
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System precision for related substances determination was verified by system suitability mixture (SSM), which was analyzed for six times and RSD of Lafutidine and all impurities peak areas were evaluated and found to be between 0.36% to 1.30%.
Figures of merit, such as selectivity, analytical sensitivity, limit of detection and precision were determined for the DCF prediction model and the determinations were verified by an independent method, HPLC.
Juveniles were distinguished from adults based on plumage characters [65], and sex determinations made in the field were verified using a PCR protocol that identifies a gene on the W chromosome [66].
The final markers of these genomic changes (amyloid-β1-42 and total τ levels) were verified by proteomic determination.
Extraction procedures were verified by nicotine determinations.
Biomass dry weights for each batch of assay vials were verified by dry weight determinations on a group of five samples co-pipetted into pre-tared vials.
The determination of constituent concentrations in dilute acid hydrolysate and enzymatic hydrolysates were verified by HPLC.
ELISA and ECL samples found positive in screening were verified by a second confirmatory assay and titre determination.
The Babesia-positive samples based on FRET-qPCR were verified in confirmatory nested PCRs and by sequence determination of the amplification products for precise species identification.
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