Sentence examples for evaluated and quantified by from inspiring English sources
g i is the channel attenuation coefficient of the link from eNB to the user i, which includes the path loss, multipath fading, and shadowing fading effects; as we say before, it is usually evaluated and quantified by the receiver and then sent to the eNB.
Cell viability was evaluated and quantified by cell counting using the trypan blue exclusion method.
The efficacy of the first and second strand cDNA synthesis was evaluated and quantified by PCR using GAPDH primers and platinium® Taq polymerase (Invitrogen) as described above.
Genomic DNA was evaluated and quantified by a Nanodrop UV spectrometer (Thermo Fisher Scientific Inc., Wilmington, DE, USA) and a PicoGreen-based fluorometric assay (Molecular Probes, now part of Invitrogen Corporation, Carlsbad, CA, USA) and stored at -80°C until analysis.
The efficacy of the first and second strand cDNA synthesis was evaluated and quantified by looking whether the 5'end of a long sized gene is amplified with the same amount as the 3' end using the 1.2 kb GAPDH gene (3' end primers: 5'-AAGGTCATCCCAGAGCTGAA and 5'-TGTGAGGGAGATGCTCAGTG; 5' end primers: 5'-CGTCCCGTAGACAAAATGGT and 3'-GTGGTTCACACCCATCACAA).
Cell adhesion, viability and proliferation onto the external surface of MWCNT/CHI scaffolds with C2C12 cell line (myoblastic mouse cell), which is a multipotent cell line able to differentiate towards different phenotypes under the action of some chemical or biological factors, has been evaluated in vitro and quantified by MTT assays.
Expression of TWIST1 and SLUG in surgical specimens was evaluated by immunohistochemistry and quantified by multiplicative score.
Fibrillin-1/MAGP-1 synthesis and deposition and the expression of αvβ3 integrin/phosphorylated focal adhesion kinase and vinculin/actin were evaluated by immunofluorescence and quantified by morphometric analysis.
The expression of GFP was then evaluated by epifluorescence microscopy and quantified by fluorescence spectroscopy.
The labeled cells were evaluated by fluorescence microscopy, and quantified by cell counting using 20 representative fields.
The obtained results demonstrate the feasibility of TSA based processes for post-combustion CO2 capture applications, and the presented methodology can be used to evaluate and quantify possible improvements provided by using novel technology elements such as alternative materials.
