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By measuring these two signals in tandem, CancerSEEK was able to detect cancer in 70% of blood samples pulled from 1,005 patients who had already been diagnosed with one of eight forms of the disease.
By measuring these two dimensions, it is then possible to place companies into four different categories based on their level of health promotion capacity.
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A calibration curve was obtained by measuring these solutions three times at each measurement.
By independently measuring these three processes under identical experimental conditions, we were able to readily decouple internalization, phagosomal acidification and phagosomal-endosomal/lysosomal fusion by simply measuring the lag between the measured rate curves for these three processes.
By independently measuring these three events under identical experimental conditions we were able to readily decouple the kinetics of both phagosomal acidification and phagosomal-endosomal/lysosomal fusion from bead internalization, a result which, to the best of our knowledge, has not been achieved previously for any class of phagocytic cells, professional or non-professional.
Furthermore, accurate and standardized methods to measure these two markers by quantitative real-time PCR (qPCR) have been described [9], [10].
However, because DINP is a mixture of isomers, it is also possible that the prevalence of exposure to DINP is underestimated by measuring only these three oxidative metabolites.
These are obtained by measuring at two different locations within a sample that is in phase coexistence.
Trueness was assessed by measuring three replicate samples on two different days.
Tumor growth was monitored by measuring two perpendicular diameters of the tumor using calipers.
S tage of life has been constructed by measuring two variables.
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