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The nature of this binding was studied using extracts of a microcystin-deficient mutant in vitro.
The role of DNA methylation in cDDP binding was studied using methylated and unmethylated plasmid incubated in vitro with cDDP.
Star-shaped PEG covalent binding was studied using static contact angle, X-ray photoelectron spectroscopy (XPS), and quartz crystal microbalance with dissipation monitoring (QCM-D).
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Changes in NKA structure in dependence on ATP binding were studied using adsorptive transfer and usual CPS at bare HMDE in the arrangement mentioned above.
The cation binding affinity was studied using colorimetric and UV Vis spectral methods for the three receptors.
The saturation binding of these probes was studied using HEK-293 cells engineered to overexpress the human melanocortin 4 receptor (hMC4R) as well as the human cholecystokinin 2 receptor (hCCK2R).
The effect of Pluronic F127 fraction and concentration of chitosan on particle size and % mucin binding of the formulations was studied using 2-factor, 3-level, central composite experimental design.
For mutants that were classified as having no specific radioligand binding, cell surface expression was studied using immunofluorescence and confocal microscopy.
The binding efficacy of each receptor was studied using NMR and isothermal calorimetric titrations in DMSO and CH3CN/CHCl3 solvent systems.
The effect of IGF stimulation on cap-mediated translation activation in mesothelioma cell lines was studied using binding assays to a synthetic 7-methyl GTP-cap analogue.
The function of malectin binding to the nascent glycopeptides was studied using wild-type and NHK alleles of α1AT (Chen et al., 2011; Galli et al., 2011).
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