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Mo structures and oxidation states are determined by preparation parameters such as loading, preparation method, calcination temperature, reduction temperature and reaction temperature [17].
Calibration graphs were first determined by preparation of different concentration of the standard solutions.
The distribution of starch phosphate in the starch granules was determined by preparation of Nägeli dextrins followed by quantitative 31P-nuclear magnetic resonance spectroscopy.
Rates of neutrophil apoptosis were determined through preparation of cytospins at 20 hours.
Tumor size was determined after preparation of the lung by caliper measurement.
The fragment size range is determined during preparation of the DNA prior to sequencing.
Bacterial counts in the milk were determined by preparation of 10-fold dilution series of milk in sterile saline.
The water content in tissues was determined during preparation of samples for metal analysis and used to normalize PAH concentration (micrograms per gram) to dry weight.
Notably, the fluorescent population also contained a fraction of developing gametocytes, as represented by low DNA content and characteristic morphology of parasites as determined after preparation by cytospin.
Recent studies have indicated that the time interval between bowel preparation and the start of colonoscopy is also important in determining bowel preparation quality.
The Taguchi experimental design method (L9 34)) was applied to determine the preparation conditions of the sol gel process.
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