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The improved catalytic activity of PDI-Co3O4 NCs for colorimetric reactions could be attributed to the synergistic effects of PDI and Co3O4 nanoparticles.
The observed increase in colorimetric response can be attributed to the nature of BEA, which exposes surface-bound enzymes to the substrate present in bulk more efficiently than b-BSA.
Attributing to this factor, the colorimetric assay analysis can be easily done via naked eye observation and without the requirement for costly high-end equipment.
The colorimetric studies supported a change in physical color attributes.
UV vis absorption and fluorescence spectra studies showed that the FLS2 as a colorimetric and ratiometric fluorescent probe exhibited high selectivity and sensitivity towards Hg2+, which was mainly attributed to the special binding with the receptor unit accompanied with the spirolactam ring-opening progress.
The visually colorimetric and "turn-on" fluorescent detection with large stokes shift (ΔF ≈ 137 nm) can be attributed to the formation of semi-rigid hydrogen-bonded complexes by intermolecular hydrogen bonding followed by activated intramolecular Br⋯HC hydrogen bonding.
Small windows show colorimetric intensity ratio.
The colorimetric reaction was stopped by adding 1 M H2SO4.
Cell viability was assessed by WST-1 colorimetric test (Roche) and cell numbers were determined using the sulforhodamine B (SRB) colorimetric assay (Skehan et al., 1990).
A colorimetric assay for the measurement of the sensitivity of herpes simplex viruses to antiviral agents.
Mitrovic, S. et al. Colorimetric screening for high-throughput discovery of light absorbers.
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