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At the early scans, ML and ML use the same windows and the RMS errors coincide as a consequence.
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The volume of evaporated extract was adjusted to 10 ml using the same solvent.
In this study, DO measurements were carried out in sample volumes ranging from 2 mL to 10 mL using the PM.
After each pickling treatment, the pickling solution volume was restored to 30 mL using the same vinegar used for pickled soybean production.
The sample was then clarified at 13,000 g for 10 min and the supernatant was brought to 50 ml using the above pellet-dissolving phosphate buffer.
The predicted left liver graft volume with the middle hepatic vein was found to be 403 mL using the region-growing method with 3D CT software.
For analysis, an appropriate aliquot from the prepared sample solutions, spiked with 300 µL TNX stock solution, was diluted to 10 mL using the same solvent.
Subsequently, the bound cells (+ve fraction) were eluted with MACS buffer (1 ml) using the plunger.
PAT volume was measured in ml using the volume analysis software tool of the Siemens Leonardo Circulation workstation.
For each participant genomic DNA was extracted from buffy-coats prepared from EDTA blood samples (9 mL) using the method of Miller [54].
50 ml of Iomeprol 400 (Imeron 400, Bracco Imaging S.p.A., Milan, Italy) were injected using a power injector with an injection rate of 5 ml/s and followed by a saline chaser of 20 ml using the same flow rate.
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