Sentence examples for compared the affinity from inspiring English sources

Commonly used florescent probes include: warfarin, phenylbutazone for site 1; ibuprofen, naproxen for site 2 and digitoxin for site 3. Miklós Poór et al. compared the affinity to HSA between flavonoids and warfarin [145].

We searched for signs of multiple interactions occurring simultaneously and compared the affinity.

In this step, we compared the affinity of antibodies for antigens presented either in solid or liquid phase.

For CR3, CR5 and CR8, we compared the affinity of lysine methyl and ethyl esters and found negligible difference in binding affinity, irrespective of the ionic strength or pH used (results not shown).

For this reason, we have compared the affinity constants of AtCERK1 (Liu et al., Science 2012) and Ecp6 as these were both determined by the same technology, ITC, and under very similar conditions.

To assess possible effects of the observed crystallographic dimerization on the EhRacC/EhPAK4 complex in solution, we compared the affinity of wild-type EhPAK4 and charge reversal mutant EhPAK4 R42D) for EhRacC·GTP using SPR.

Finally, we evaluated drug binding affinities using Prime/MMGBSA and using these scores we compared the affinities of combination therapies against MDR1.

We compared the affinities of this peptide with the non-phosphorylated version (Atx1_S_ULM_PE) and with the shorter Atx1_pS_ULM peptide.

We further compared the affinities of the different combinations of Sti1/Hop with Hsp90 by surface plasmon resonance spectroscopy (SPR) (Supplementary Fig S2).

We measured the dissociation constants of several putative CAP binding sites by EMSA (Electrophoretic Mobility Shift Assay) and compared the affinities to the bioinformatics scores provided by methods like the weight matrix method and QPMEME (Quadratic Programming Method of Energy Matrix Estimation) trained on known binding sites as well as on the new sites from SELEX SAGE data.

Two solid-phase binding assays were designed and evaluated for their potential use in comparing the affinity of peptides to the Src SH2 domain.