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In our tests, the worst case can be 8-10 ml for each 100 ml.
I suspect that calculating the ML for each channel is important because it allows us to detect derviatives in areas that may have uniform total luminance, but varying color (like the texture of the striped cone).
Erythrocytes were maintained 108 cells per mL for each assay.
It actually means the coverage, Θ, of 0.125 ML for each surface.
After centrifugation and aspiration of the supernatant, the cell was fixed in ice-cold 96 100% ethanol approximately 1 ml for each sample.
The volume was depending on a ratio of 0.5 mL for each 2 cm of lesion size or a quarter volume of the lesion.
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We adopted 20 ml of DNA at a concentration of 50 ng/ml for each array.
The calibration curves were linear over 0.100 20.0 ng/mL for each enantiomer.
The calibration curves in plasma were linear over the range of 5 500 ng/ml for each enantiomer with detection limit of 2 ng/ml.
The LC/MS/MS method was found to be accurate and precise within the linear range of 1.0 2000 ng/ml for each analyte in enzyme incubation mixture.
A capillary zone electrophoresis method has been developed to quantify the enantiomers of ofloxacin in high diluted samples (20 700 ng/ml for each enantiomer).
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