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The different results for the mono-, bi-, and tri-layer graphene are theorized to be caused only by the variation among the diffusion barriers of the various graphene layers, which provides a method of determining the number of graphene layers and provides information that can be utilized to elucidate the interaction between a graphene flake and its substrate.
Here, we outline a medium- to high-throughput siRNA-based approach that, in combination with real-time bioluminescence measurement of a circadian reporter gene, can be utilized to elucidate the effects of gene knockdown across several days in human cells.
Thus, FRET can be utilized to elucidate dynamic conformational changes of biomolecules in microscopic detail [ 1– 4, 14].
Mouse models can be utilized to elucidate the genetic and molecular basis of human gastrointestinal disease and to test therapeutic and chemopreventive compounds.
As such, this system can be utilized to elucidate systematically the effects of individual chemical cues in addition to gradients of multiple cues on individual cell behavior, as well as to spatially direct 3D stem cell differentiation.
Furthermore, the ability of miR-210 to regulate hypoxia-mimic response by binding to target genes could be utilized to elucidate the health effects of a variety of heavy metals that induce HIF-1 α stabilization.
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An idealized one-dimensional configuration is utilized to elucidate this process.
A variety of analytic methods are utilized to elucidate the structure and dynamics of supramolecular nanoassemblies.
The high speed recording technique was utilized to elucidate the fluid dynamics of two-phase flow splitting at microchannel junctions.
Reaction flux and sensitivity analysis were utilized to elucidate chemical kinetic features of ECH combustion under various reaction conditions.
The high speed recording technique was utilized to elucidate the fluid dynamics of two-phase flow in parallel micro-channels.
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CEO of Professional Science Editing for Scientists @ prosciediting.com