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Preserved samples were assayed for PHA content.
Blood samples were assayed for NEFA and BHBA concentrations.
Results: Thirty samples were assayed for each storage condition.
The samples were assayed for the SCR of NOx with methane in excess oxygen.
At the end of each treatment, samples were assayed for CIPDI activity at pH 7.5 (A).
Saliva samples were assayed for cortisol (C), dehydroepiandrosterone (DHEA), and testosterone (T).
Plasma samples were assayed for ED-B fibronectin by enzyme-linked immunosorbent assay.
Fasting blood samples were assayed for putative biochemical risk factors and urine samples for microalbuminuria.
Samples were assayed for IL-10 by commercially available ELISA and for for 17β-estradiol and progesterone by RIA.
Thirty oocytes composed one sample and three samples were assayed for each treatment.
Samples were assayed for their content in PGE2 by ELISA (Assay Designs, Brockville, ON, Canada).
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