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Competitive displacement FP assays performed with and without PreserveX-QML For pharmaceutical drug discovery studies, it is critical to establish that incorporating membrane proteins into a new amphiphilic medium does not alter their quantitative biological properties (such as binding characteristics)

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Commonly, transporter binding and utilization by the nanocarriers has been evaluated by the inhibitory effect of a competing substrate or inhibitor of the targeted transporter (Table 3)

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