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We found that the association is enhanced by increasing both the ionic strength and the anionic phospholipid fraction.
For this purpose, the role of both the ionic strength and the overpotential were investigated in blocking electrode conditions, i.e. only in the presence of the supporting electrolyte.
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We have observed that the isoelectric point (IEP) of the membrane materials is both dependent on the ionic strength and on the kind of electrolyte solution.
However, the model parameters are solvent dependent so a prerequisite for its true applicability is that binding is both Langmuirian and essentially independent of the ionic strength of the feedstock applied.
Lowering the ionic strength of the bathing solution enhanced potentiation, suggesting that it involves electrostatic interactions.
Despite the large discrepancy between the ionic strength of Exp.
Salt concentration is directly proportional to the ionic strength.
Furthermore, increasing the ionic strength stabilized the assembly of the K14/A mutant.
Again, the dissociation constant was shown to be independent of the ionic strength (Fig. 2C).
By increasing the ionic strength, this salt destabilizes electrostatic interactions whereas it reinforces hydrophobic interactions.
Septin polymerization depends on the ionic strength.
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