A thermal cycle consisting of a 54 min run and subsequent a 6 min pause was repeated four times, and a processed specimen was analyzed in terms of the deposition and oxidation of the substrate.
However, a formal statistical analysis is not presented and only a single tumour specimen was analyzed.
Each individual isolate within an eae-positive specimen was analyzed by using a multiplex PCR to confirm the presence of eae, and also to test for the presence of genetic markers of typical EPEC (bfpA), Shiga toxin producing E. coli, and/or enterohemorrhagic E. coli (EHEC) (stx1, stx2, ehxA).
A wet-mount specimen was analyzed for the presence of clue cells under 40 × magnification [ 16].
A sample of 100 μL of the supernatant from each specimen was analyzed in a UV-Visible spectrophotometer to determine the amount of methylene blue leakage.
In a recent study, the number of norovirus cDNA copies per gram of stool specimen was analyzed and a discrepancy was found between the different norovirus genogroups (10 ).
Every collected specimen was analyzed under a stereomicroscope and identified using the taxonomic key developed by Teskey [11].
The grain orientation of each specimen was analyzed by an electron back-scattered diffraction (EBSD) method.
A complete calibration check was made after the last specimen was analyzed.
The skin specimen was analyzed for phospho-c-Jun.
Each specimen was analyzed for MDA and creatinine.
