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Tetraphosphonate cavitand host (4iPO 1) was shown to impact more markedly n-Bu4NCl reactivity than triphosphonate counterpart (3iPO 3) due to its greater binding strength toward the ammonium cation as evidenced by titration experiments.
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In general, the binding strength of complementary strands toward the unmodified DNA sequence was higher than the modified sequences.
The binding strength and the number of binding sites were determined at different ionic strengths.
Sites were sorted for binding strength within the three subsets.
The binding strength is determined by the binding free energy, Δ G bind.
So the translocation probability of the species with conserved binding strength went through some maximum while reducing the binding strength of its competitor [27].
An antibody can recognize its antigen, and can evolve toward the immunogen to increase binding strength, in a process referred to as affinity maturation.
The binding strength was significantly weakened by carboxymethylation.
"For an effective drug, you would want to increase the binding strength significantly.
We analyzed in detail the binding strength for maximal flow.
To circumvent this problem, we interpret the binding strength or specificity comparatively among different HAs or compare relative binding strength or specificity to a reference HA.
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CEO of Professional Science Editing for Scientists @ prosciediting.com