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F− was detected through the formation of hydrogen bonds and the subsequent deprotonation process.
For this purpose, the effect of Kif4A on CCL2-STAT3 pathwas was detected through western blot analysis.
During reduction, a stable electro-active species was detected through CP and SWV.
Cellular adhesion was verified and cellular response to an induced electrode strain of 1% was detected through fluorescence microscopy.
Fluorescence was detected through the objective (LUMPLFLN 60XW, Olympus, Hamburg, Germany) and the oil-immersion condenser (1.4 NA) using GaAsP-PMTs (Hamamatsu Photonics, Hamamatsu, Japan).
Sequence-specific hybridization of target uropathogen 16S rDNA was detected through horseradish peroxidase acting as an electrochemical transducer via a second, detector probe.
A pool with four dengue serotypes (DENV-1, -2, -3, -4) was detected through antigen-antibody binding using gold nanoparticles (AuNPs) as signaling antibody carriers.
The onset of steady state was detected through analysis of the solid phase by means of Focused Beam Reflectance Measurement (FBRM).
In 40.6% of cases, bleeding was detected through the patient's call for assistance, and in 59.4% of cases nurses noted bleeding while checking the puncture site.
The modified surface was detected through the change of hydrophobicity and thickness of MPTMS using the contact angle measurement and ellipsometry techniques.
The 532 nm probe light was detected through a 550 ± 40 nm band-pass filter by an OP-2 photocurrent-type semiconductor sensor connected to a FieldMaxII-TO controller (Coherent Japan Corp., Japan).
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