h Adiponectin level in medium were measured by ELISA.
Cytokine concentrations in culture medium were measured and expressed as mean ± SD of three independent experiments.
First, the particle size and surface charge of silica particles in water and medium were measured.
Glucose and glycerol concentrations in medium were measured by using the assay kits.
The amounts of lactate and the pH value (acid) of the PLGA and PLLA degradation medium were measured.
The cell pellets and the medium were measured in a gamma counter to determine cellular uptake % uptake = 100 × cpminpellet cpminpellet + cpminsupernatant (1).
Artificial pond water was replaced every second or third day during all experiments; the oxygen content and pH in the old and new medium were measured.
Nitrite and nitrate levels in the culture medium were measured, and inducible-type NO synthase (iNOS) and nitrotyrosine were determined by immunofluorescence staining.
Linear burning rates of quasi-homogeneous mixtures of μAl and liquid water as a function of pressure, mixture composition, density and environment gas medium were measured.
The physical properties, porosities, permeabilities, capillary pressures, and end-point saturations of the blocks composing the heterogeneous medium were measured independently on isolated samples.
Thickness of each medium layer and velocity of ultrasonic wave propagation in each medium layer of the two-layer composite medium were measured simultaneously based on the method to collect phase information from continuous echo signals on front surface and undersurface.
