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Using diethylene triaminepentaacetic acid (DTPA) as complexing ligand, the fabricated electrode displays a well-defined and highly sensitive peak for the reduction of Cr III)–DTPA complex at −1.06 V (vs. Ag/AgCl) with a linear concentration range of 0 25 nM and a fairly low detection limit of 0.036 nM.
Thus, the technical replicates act as a powerful filter to produce a more adequate peak list from one originating from an overly sensitive peak detection.
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So, acetonitrile was the organic modifier of choice giving symmetrical highly sensitive peaks in a reasonable time.
So, n-propanol was the organic modifier of choice giving good resolved and highly sensitive peaks within a reasonable time (less than 6 min).
Concentrations less than 6% resulted in a broad and less sensitive peaks and it was time consuming, whereas concentrations higher than 14% decreased number of theoretical plates for both drugs.
Thus, CLIPdb also provides alternative binding sites identified using other more specialized strand-sensitive peak-calling tools (e.g., CIMS package for HITS-CLIP and iCLIP, and PARalyzer for PAR-CLIP).
It is also somewhat more sensitive, with peak sensitivity at 600 nm (0.57 quantal efficiency).
In some contrasts, DDA measures were significantly less sensitive than peak scoring, and in two contrasts, CDA 2 was significantly more sensitive than peak scoring.
A sensitive oxidation peak at 0.085 V was observed in the determination of l-serine and 0.06 V for l-phenylalanine.
X-ray photoelectron spectroscopy was used to identify the origin of a unique, radiation sensitive diffraction peak observed in some LARC-CPI films.
In the as-prepared BAgNP sol substrate and in the presence of NaCl, ST molecules adsorbed on the surfaces of AgNP/AgCl aggregation by hydrophobic and intermolecular forces and exhibited a sensitive SERS peak at 1535 cm−1 that could be used as a SERS probe to monitor the ST concentration changes in the catalytic reaction system.
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