Sentence examples for binding affinity of different from inspiring English sources
We present a computational investigation of binding affinity of different types of drugs with chitin nanocarriers.
Recent work has focused on the binding affinity of different strains of influenza virus for specific cell receptors within the respiratory tract [18] [21] and it is believed that this difference in affinity between human and avian strains may in part be responsible for the difference in severity between the two strains, though the reasons for this are currently not well understood.
Here, however, by measuring the binding affinity of different export-competent NES for Crm1, we find no evidence of a correlation between Crm1 affinity and the ability to potentiate CSR.
Techniques from the signal-processing field were used, in particular the Hann digital filter, to calculate the relative binding affinity of different regions based on previously published in vitro binding data.
The oxygen binding affinity of different combinations was epistatic, such that the HHH, LLL and LHH combinations showed the highest affinity while for all other combinations lower values were reported.
In this study we adapted a commercial ELISA kit for use with other species: we evaluated the binding affinity of different conjugates to IgG of the target species, ensured the absence of non-specific binding after modifications, performed a checkerboard test to recommend optimal sample and conjugate dilutions, and determined appropriate cut-off values.
Although Ehrlich himself described the observation of the lack of staining, his thoughts were not as insightful as Ridley's in 1695 since he presumed, as mentioned above, that the difference was due to the different binding affinities of different tissues to different dyes.
To investigate enzyme ligand interactions in yeast hexokinase isoform PII under physiological conditions, we utilized the technique of Saturation Transfer Difference NMR (STD NMR) to monitor binding modes and binding affinities of different ligands at atomic resolution.
Here we evaluate the performance of a molecular dynamics based method for predicting the binding affinities of different types of human thrombin inhibitors.
Discrepancies are found between the results of the binding affinities of different new TSPO radiotracers, and they showed heterogeneity in binding potentials in humans [9, 16, 41, 42].
