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The experimental cloud point data were determined using titration method.
Data were determined using membrane preparations of CHO cells stably transfected with the respective sst subtype.
Solubility data were determined using a simple and reliable apparatus and analyzed by the classical titration method.
After the reaction, the cycle threshold (CT) data were determined using fixed threshold settings, and the mean CT of the triplicate PCRs was determined.
After the real-time PCR reaction, the cycle threshold (CT) data were determined using fixed threshold settings; the mean CT was determined from triplicate PCRs.
On the basis of the above analysis, trends in the time-series data were determined using the minimum L1-norm condition (Menke, 1989).
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The surface sag data is determined using genetic algorithm method.
The accuracy of the experimental density data was determined using Standing and Katz method.
The statistical analysis of the obtained data was determined using the Co-statistical software package [26] by analyzing the variance (one way completely randomized, ANOVA).
Distribution of data was determined using Kolmogorov-Smirnov test.
The Ct data was determined using default threshold settings.
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