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A total of ≈500 cells were assessed for each strain.
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Non-inferiority and superiority objectives were assessed for each vaccine strain by estimating GMT ratios (QIV / TIV) 21 days after vaccination.
One hundred cells were assessed for each probe.
Thus, metabolic clustering was only assessed for this strain.
To confirm the seroconversion observed by the IHA, immunogenicity was assessed for the H1N1 strain by ELISA.
The kinetic parameters were assessed for several microalgal strains (Stichococcus bacillaris, Scenedesmus vacuolatus, Chlamydomonas reinhardtii, Chlorella vulgaris) growth in vertical and inclined bubble columns and irradiated by white-light or red/blue light.
Antibiotic susceptibility was assessed for all separate strains when quantitative cultures revealed ≥ 10cfu/mll.
A complete analytical model, which incorporates shear deformation as well as transverse normal thermal strains is assessed for the thermal stress analysis of cross-ply laminates subjected to linear or gradient thermal profile across thickness of the laminate.
DNA-DNA hybridization was assessed for isolate against reference strain Rhizobium radiobacter DSM 30147T (= AB247615) that showed 97% sequence similarity.
To assess biofilm forming for each strain and negative control, the arithmetic mean of absorbance and standard deviation were used.
For example, when 310 strains of T. reesei other than the industrial strain were assessed for their ability to deconstruct switchgrass, one strain was found capable of outperforming commercial enzyme preparations [ 16].
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