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A crystalline-like organization of the molecules allows high current density but low luminance efficiency since an excessive electron current flow is involved compared to the hole one, and the recombination rate is poor.
The small size of molecules allows high device density in the range of 1011 to 1012 devices/cm2[1].
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Although electroporation allows high internalization efficiencies to be achieved, the amount of non-internalized fluorescent molecules that remain in cell suspension after electroporation is typically much higher than the amount of internalized molecules.
Endothermy allows high levels of sustained activity.
In this model, initial weak binding to MHC molecules would allow higher-affinity binding only to those ligands to which the best fit could be obtained before the encounter complex dissociates.
Thus, the combination of structural fragments of calixarenes and crown ether in one molecule allows achieving high efficiency and selectivity of ammonium cation binding.
AFM allows high-resolution, single-molecule imaging of DNA with minimal sample preparation.
Protein-labeling technique allows high-resolution visualization of molecules inside cells.
This robust assay allows high-throughput screening to discover both small molecules and antibodies targeting HER3.
Next-generation sequencing also allows high-resolution comparisons of the "transcriptome"–a profile of the RNA molecules present at a particular moment in time in healthy and cancerous cells.
"The physics of Ka allows higher throughput.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com