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BSA was the most efficient compound in reducing inhibition of amplification, due to its binding efficiency.
The reasons for the increase in binding efficiency are explained.
Initially, a proof of concept was conducted to investigate the binding efficiency of the anti-Ubiquitin (αUbi) scFv phage towards rUbi in the complex microenvironment during biopanning.
These results suggest that a higher binding efficiency to CSA rather than reduced antigenicity might provide a biological advantage to parasites with high parasite density signatures in VAR2CSA.
The binding efficiency was confirmed by the fluorescence intensity in each microtire plate well.
It was found bFGF binding efficiency to PLGA was enhanced by CO2 plasma treatment.
mIFP showed intermediate, while monomeric miRFP670 and miRFP703 exhibited high binding efficiency of endogenous biliverdin chromophore.
The study resulted in identification of putative inhibitors of PfCS with binding efficiency in nanomolar range.
Replacement of the other phosphate however strongly affected binding efficiency and selectivity.
Furthermore, we detail the optimization of a screening hit using ligand binding efficiency and log D.
binding efficiency index.
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