Sentence examples for sizes were calibrated from inspiring English sources

The gel image was analysed using 'Imagequant software™'(Molecular Dynamics, Foster City, CA, USA) and fragment sizes were calibrated to known fragment sizes in HyperladderIV (Bioline™, London, UK) which was run in duplicate on every gel.

Allele sizes were calibrated to the allele sizes of reference isolates kindly provided by Drs Lees and Cooke of the Scottish Crop Research Institute, UK [ 52].

DNA fragments were automatically sized with GeneMapper™ v4.0, and allele sizes were calibrated to the allele sizes of reference isolates (C1 C12) kindly provided by Drs A.K. Lees and D.E.L Cooke James Hutton Institutee, Dundee, UK).

These markers were amplified by the following cycling conditions: pre-PCR of 5 min at 96 °C, 1 min at 57 °C, and 1 min at 72 °C; followed by 30 cycles of 96 °C for 45 s, 57 °C for 45 s, and 72 °C for 1 min; with a final extension at 72 °C for 5 min. Amplicons were separated using the ABI Prism 3700 DNA analyzer, and allele sizes were calibrated with the GeneScan 500 ROX size standard.

The image pixel size was calibrated so that the interatomic separations in this region match the known crystallographic separations.

The needle size was calibrated according to the animal size and thymus localization.

The box size was calibrated so that the solvation shell extended at least 7.5Å (∼thickness of three water layers) from the protein surface at all times.

DNA fragment size was calibrated using two sets of pulse markers: chromosomes from Saccharomyces cerevisiae (225 2200 kbp) and a mixture of lDNA Hind III fragments, lDNA and lDNA concatemers (0.1 200 kbp) from Sigma.

Drop size was calibrated to about 7 8 nl / injection.

Pure HepOH was used and the drop size was calibrated to 20 nl / injection.

In brief, the sample size was calibrated to develop and validate a risk-stratification system to predict 7-day all-cause mortality.