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Two key parameters relevant to on-chip biochemical assays and microfluidic sensors are studied and compiled: the capture fraction of the bulk analyte at the surface and the saturation time scale of the reactive surfaces.
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A theoretical model including both transport and reaction kinetics is employed to study the influence of flow velocity, bulk analyte concentration, analyte diffusivity, and adsorption rate on the performance of open-ended and closed-ended porous sensors integrated with flow cells.
The effects of flow velocity, bulk analyte concentration, analyte diffusivity, and adsorption kinetics on sensor response are simulated and compared between the two different flow schemes.
Two-color excitation setups could investigate competitive interaction between multiple analytes at the stationary phase interface.
However, quantification has not previously been done with analytes at the peptide level.
Carbon dioxide bulk temperature at the outlet of the tube.
The effects of decomposition of the analyte at higher temperatures and adhesion of the analyte on the diffusion column at lower temperatures during the measurements are briefly considered but have only a small impact on the present systems.
The detection is limited in the number of analytes monitored as detection of any one analyte is at the expense of any other.
We note that although the flow-through configuration with open-ended pores maintains approximately fivefold improvement in equilibrium time throughout the simulated concentration range, the impact on time saving by the flow-through scheme is stronger for analyte at lower bulk concentrations.
There was no fetal sex-based difference in analyte concentrations at the postpartum measurement.
Favor skirts without much bulk at the waist.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com