Thirty-seven samples were checked for three types of human adenovirus, as well as rotavirus, enterovirus and fecal coliforms.
The brick samples were checked for dimensions and visible defects.
At the end of each treatment, samples were checked for CIPDI activity.
The phases of corresponding samples were checked by XRD with Cu Kα of 0.1542 nm radiation.
Five samples were checked for the presence of horse DNA above a 1% threshold.
The 160 outpatients' DNA samples were checked with QDs and superparamagnetic nanoparticle-based hybridization and type-specific PCR.
Cell samples were checked regularly for the expression of glial fibrillary acid protein, a marker for astrocytes.
Five samples were checked for the presence of horse DNA above a 1% threshold under a UK-wide programme.
The samples were checked for structural and morphological organization using differential scanning calorimetry, dynamic mechanical thermal analysis and scanning electron microscopy.
The consistency of the results for the same analytes samples were checked by repeating the experiment for 6 times per day (intraday) and consecutive for 3 days (interday).
During this time, aliquoted samples were checked for residual activities and no significant inactivation of PepP was observed (97% residual activity; data not shown).
