Transporter test systems have varied expression of transporters., For example, an overexpressing test system (e.g., MDR1-MDCK) may have higher functional activity for P-gp than a cell line derived from a relevant organ phenotype (e.g., Caco-2). What effects and/or difference would you expect when assessing substrate potential and inhibition potential in each of these in vitro models?
Already registered? Login
Not Account? Sign up
Enter your email address to reset your password
Back to Login? Click here