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Exact(7)
For GR DBD binding to κBREs, a two-site binding model was used.
For kinetic constant determination using the PA-immobilized chip (direct-format), a bivalent analysis model was applied, whereas, for the anti-human/anti-mouse chips (indirect-format), a 1∶1 Langmuir binding model was used.
For the binding of TOG1 and TOG2 to αβ-tubulin, a simple bimolecular binding model was used.
A one-site binding model was used to fit the data and infer binding affinity in Graphpad Prism.
The BIA evaluation software (GE Healthcare) assuming the Langmuir 1 1 binding model was used to analyze the data.
Global fitting using a 1 1 Langmuir binding model was used to calculate the association rate constant [ ka (M−1·s−1)] and dissociation rate constant [ kd (s−1)] (Table 1).
Similar(53)
A new multi-state SMA binding model is used for testing this hypothesis.
A tight-binding model is used to explain the various band structures in different CKLs.
A simple tight-binding model is used to describe the system and all the calculations are done based on the Green function formalism.
A simple tight-binding model is used to describe the system, and all the calculations are done through the Green's function formalism.
A simple tight-binding model is used to describe the system and all the calculations are done based on the Green's function formalism.
More suggestions(20)
binding model was analyzed
binding activity was used
binding model was constructed
binding stability was used
binding distance was used
binding site was used
binding model was determined
binding capacity was used
binding protein was used
binding model was speculated
binding sequence was used
binding model was fitted
binding equation was used
binding fit was used
binding model was developed
binding assay was used
binding probability was used
binding model was proposed
binding assumption was used
binding energy was used
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