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The magnitude of K suggests that 1 preferentially binds C70 in comparison to C60 although average value of selectivity in binding is measured to be low (∼1.75).
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ATP binding was measured at 10 °C to avoid hydrolysis of the nucleotide.
The binding is measured by the location of the so-called Fermi level of electrons in the metal; the higher the level, the lower is the binding.
Finally, peroxisome proliferator activated receptor gamma (PPARγ) binding activity was measured to check the binding affinities of both TGZ and TSN.
The binding capacity was measured to be up to 44.45 mg (fluoride)/g (NPs) (10 times higher than 4 7 mg/g observed for hydroxyapatite [16,25]).
The kinetics of ligand binding by the flash photolysis method was measured to determine functional properties of the BflGb4 globin.
A weighted regression that accounted for this experimental design feature was used in fitting a nonlinear dose-response exponential model to the PCB concentration-activity data from an in vitro test system in which 3H-phorbol ester binding was measured in cerebellar granule cells exposed to different PCB congeners to test for their effects on protein kinase C translocation.
After each incremental addition of the solution in the syringe, the integrated heat change due to binding was measured.
Finally, the rate of binding was measured, by exposing the fusion proteins to immobilised VEGFR2 ΔKD m for short times before washing out the protein and measuring how much fusion protein was bound.
Test labeling of the two double mutants was done with two rhodamine isomers, 5-IATR and 6-IATR (5- and 6-iodoacetamidotetramethylrhodamine), and the fluorescence response to ADP binding was measured.
The level of antibody binding was measured on the Licor Odyssey system and normalized to actin.
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CEO of Professional Science Editing for Scientists @ prosciediting.com