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Surface plasmon resonance (SPR) analysis was used to determine binding kinetics of the two clones (3-1D2 and 3-1F6) representheg two two different sets of isolated complementarity determining region (CDR 3s.
A MicroCal VP-ITC was used to determine binding parameters of biotin and desthiobiotin to BPL.
Saliva based ELISA assays were used to determine binding of the outbreak virus to saliva samples.
A standard ELISA was used to determine binding of mAbs to the panel of HIV-1 Envs.
qPCR was used to determine binding by use of primers flanking binding site.
The W67,68 mutant was used to determine binding constants at the nonannular sites on KcsA.
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Fluorescence quenching methods in combination with Fourier transform infrared (FT-IR) spectroscopy and circular dichroism (CD) spectroscopy was used to determine the binding mode, the binding constant and the protein structure changes in the presence of genistein in aqueous solution.
However, very few of these studies have moved beyond the traditional Langmuir binding model used to determine thermodynamic binding affinity for monovalent interactions, and to our knowledge there is no study of the dependence of the binding kinetics on bulk PnA concentration.
Here fluorescence binding assay was used to determine the binding activity of AfunOBP1 and AfunOBP3 to the EAG-active compounds.
A competitive radiolabeled receptor binding assay was used to determine the binding affinity of the cRGDfk peptide on the QD surface to ABIR.
Western blot and ELISA plate binding assay were used to determine the binding activity of rMsEno to chicken Plg (Cell Sciences) and human Fn (Sigma-Aldrich).
More suggestions(15)
used to calibrate binding
used to measure binding
used to compare binding
used to define binding
used to predict binding
used to think binding
used to infer binding
used to demonstrate binding
used to confirm binding
used to perform binding
used to assess binding
used to extract binding
used to probe binding
used to evaluate binding
used to model binding
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