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The CILP-2 competitive assay had an intra assay variation of 11.1% and the inter assay variations for high control was 20.7% and for low control 22.2%.
Control samples were measured as 2.0 and 2.3 nmol/L for low control (range 1.6. - 2.6 nmol/L) and 6.5 and 8.1 nmol/L for high control (range: 6.3 - 10.4 nmol/L).
Control samples were within the range indicated by the manufacturer: 14.9 and 15.4 U/L for low control (range 9.8 - 21.1 U/L); 64.3 and 86.6 U/L for high control (range 62.0 - 97.2 U/L).
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Also, this configuration allows for higher control versatility for grid codes compliance.
Future work includes time delay compensation of the converter time constant for higher control accuracy and studying potential combination of other successful methods like robust control considering parameters uncertainty.
Intraassay CsV were 3.6% for low-control sample and 3.3% for high-control sample, whereas interassay CsV were 3.2% for low-control sample and 7.3% for high-control samples, respectively [ 13].
Inter-assay and intra-assay CVs for NAGase activity were for the high control <5% and for the low control 7%.
Two controls were provided and the coefficient of variation for all kits used was 17% for the low control and 18% for the high control.
Since 1% Triton-X is known to be toxic for cells, it was used as a positive control for LDH activity (high control) and hence maximum toxicity.
In this paper, a common sharing method for current and flux-linkage control is proposed for high performance control of the switched reluctance motor (SRM).
Control input time delays are becoming critical as the demand for high frequency control actions is increasing.
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