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Cell concentrations of the samples were determined using a Sysmex XE2100 haematology automated analyser.
The concentrations of both undiluted and diluted samples were determined using a DeNovix DS-11+ Spectrophotometer (Saveene Werner) following the manufacturer instructions.
The morphology pristine and modified samples were determined using atomic force microscopy (AFM).
Length and width of the samples were determined using this system.
pGH concentrations in the released samples were determined using a standard MicroBCA method.
The thermal properties of the samples were determined using differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA).
The common anions and cations in mineral water samples were determined using this ion-chromatographic system with satisfactory results.
The radionuclide content (226Ra, 232Th and 40K) and radon massic exhalation of HVFAC samples were determined using gamma spectrometry.
Zeta potential of the samples were determined using ZETA POTENTIAL METER, MFGPRO-52400035.
Crude protein of diet samples were determined using method 990.03 (AOAC 2000).
Yield and quality of the RNA samples were determined using a NANODROP 2000 spectrophotometer (Thermo Fisher Scientific, USA).
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