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To identify and locate diffusive regions, we develop metrics for measuring transport effects that are based on the quasidiffusion (Eddington) factor.
Finally, because results are expressed in units of travel costs, the average weighted impedance may easily be misinterpreted as exclusively measuring transport system performance, while other components,, e.g. the spatial distribution of opportunities and its amount, are ignored.
Although simple in concept, proving this model has proven to be difficult due to the absence of suitable in vitro models for measuring transport through tissues and across vascular basement membranes.
These assertions are based, however, on work measuring transport of uracil, cytosine, and thymine and their derivatives, not of ADP or ATP [ 249].
The proteins and genes for all plastid transport proteins may not have been identified yet, in part because of the difficulty of measuring transport by membrane proteins to verify their function.
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Because the measured transport rate included both heterologous and native S. cerevisiae transporters, the determined kinetic constants refer to the overall cellular transport capacity.
However, during aerobic cultivation at 4 g/L xylose, the measured transport kinetics were mirrored, in the sense that expression of the Gxf1 transporter led to the largest increase in growth rate, followed by the Sut1 transporter.
Two-terminal device was fabricated from MoS2 nanotubes to measure transport properties (Figure 4a).
The measured transport rates (Q) obtained from the passive traps ranged from 0.70 to 32.63 g/m/s.
In this study, the microperfusion system was used to measure transport properties of porcine adipose-derived stem cells (pADSCs) membrane.
This property is crucial for the fabrication of atomic-precision donor-based devices where the aim is to measure transport through atomically positioned single dopants [16].
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