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Even in the case of ionizable drugs, where Kow tends to underestimate membrane affinity, the latter can be correctly quantified using solid-supported lipid membranes: data comparison shows good agreement of the presented approach with established but time-consuming standardized lipid/buffer systems.
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For VvHT11 signals obtained with Northern blot were too low to be correctly quantified.
Proteins were quantified using Qubit® 2.0 Fluorometer.
Immunoblots were quantified using ImageJ.
Fluorescence was quantified using ImageJ.
Cell size was quantified using SigmaScan Pro.
OPA1 fragmentation was quantified using AIDA software.
DNA was quantified using ultra-violet quantification.
cRNA was quantified using the Nanodrop spectrophotometer.
Total RNA was quantified using Qbit.
RNA samples were quantified using spectrophotometry.
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