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Three working standards calibrated to VSMOW and standard reference waters supplied by the International Atomic Energy Agency IAEAA) were analyzed in duplicate with each batch of water samples analyzed.
At ANMC, a Real-time quantitative RT-PCR amplification methodology (QPCR) has been developed in which HCV viral loads are determined by interpolation of QPCR results to those of standards calibrated to the World Health Organization (WHO) First International Standard for HCV.
To quantify total TH, in house standards (calibrated PC12 cell extract) are used to interpolate sample immunoreactivity to anti-TH versus a standard curve of known quantities of TH and the value is expressed as ng TH per ug total protein loaded [25], [27], [50], [51], [57].
Laboratory standards calibrated with values of −51.45‰ and 763.24% relative to standard mean ocean water (SMOW /standard light antarctic precipitation (SLAP) (147.75 and 274.64 ppm) were run as unknowns and the true enrichment of the analyzed samples calculated from these.
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It was measured with 129I and 137Cs standard calibrated sources as recommended [11].
The well counter sensitivity and the position of a reference energy peak were controlled monthly [11] with standard calibrated sources of 129I and 137Cs.
The possibility of use of standard calibrated scales with the presented encoder to solve existing and new industrial tasks forms the value of this paper.
This paper presents the full research and development cycle of a high-precision absolute linear encoder based on a standard calibrated scale.
Based on the recommended measurements of 137Cs and 129I standard calibrated sources, the variability of the well counter sensitivity was evaluated to be less than 1% over 4 years.
Height and Weight of the selected children were also measured using standard calibrated instruments.
A pooled plasma standard, calibrated against the UK standard (UK National Institute for Biological Standards and Control, South Mimms, UK), was employed.
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