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CNQX was purchased from Tocris (http://www.tocris.com) and added prediluted from a concentrated stock solution and to the superfusate at the final concentrations indicated.
The drugs were diluted from concentrated stock solutions and added to the superfusate at the final concentrations indicated.
Similar brain and plasma β1 concentrations indicated robust antibody efflux from the brain.
Fecal analysis of Cr concentrations indicated no difference (P>0.05) in OM, DM, or N digestibilities.
The relation between the product and reactant concentrations indicated that the hydrolysis reaction with immobilized lipase follows Michaelis Menten kinetics.
Fluorescence polarization of the Fl/SAZrP assemblies at varying Fl concentrations indicated depolarization of the emission at high loadings.
Purified ΔN-TClpB (1 μM as hexamer) in a buffer (50 mM MOPS pH 7.5, 20 mM KCl, 5 mM MgCl2) was incubated at 25 °C, and Mant-ADP was added at concentrations indicated in Supplementary Figure 8.
Yet, plasma and intracellular drug concentrations indicated that some participants had evidence of recent pill use.
Further, passive sampling-based estimates of interstitial water concentrations indicated that SWNT reduced PCB bioavailability.
The measured volatile fatty acids concentrations indicated that hydrolysis was the reaction limiting step.
Oseltamivir phosphate (OP) free base (Hoffmann-La RONhe Ltd, Mississauga, ON, Canada) was used at the concentrations indicated.
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