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Protein carbonyl content of plasma samples was analyzed using an OxyBlot protein oxidation detection Kit (Millipore).
First, a set of all genes with a minimum expression of 10 TPM summed over all samples was analyzed using random forest.
Mercury in various samples was analyzed using the cHN-Eu2O3 suspension.
The SP concentration in the samples was analyzed using an enzyme-linked immunosorbent assay (ELISA).
The structure of as-deposited and annealed samples was analyzed using X-ray diffraction.
The crystal phase of the samples was analyzed using X-ray diffraction (XRD).
The crystallization behavior of the samples was analyzed using regular and high-pressure differential scanning calorimeters and using a rotational rheometer under small amplitude oscillatory shearing.
The porosity and pore size distribution of composites were measured by Mercury Intrusion Porosimetry, and the microstructure of samples was analyzed using a Scanning Electron Microscope.
The catalytic reactivity of the samples was analyzed using a homemade reactor coupled to a combined system of Fourier transform infrared spectrometer (FTIR) and mass spectrometer apparatus.
Differential expression of two samples was analyzed using the DEGseq (Anders and Huber 2010) R package.
COD of the samples was analyzed using the procedure given in APHA (1998).
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