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The samples were afterwards heat treated to develop crystalline structures, for better identification of the units that build up the network.
Blood samples were afterwards drawn from a peripheral vein.
Blood samples were afterwards analyzed by the methods further described.
The samples were afterwards stored in 0.1 M PB containing 0.1%% NaN3.
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The sample is afterwards placed with the metallized face covered in a nickel sulfamate bath at 50°C.
The sampled bones were afterwards reassembled with plaster (Figs. 3, 4).
The samples were removed afterwards and subjected to tensile testing (n = 18).
Thirty-five (3%) extra samples were received afterwards from these clusters.
A second dose of drug was then added and samples were taken afterwards.
For treatments, 25% w/ w toothpaste slurries in water (application time 60 s) or full-strength mouthwashes (application time 30 s) were used and samples were washed afterwards by twice dipping in water.
Afterwards, samples were rinsed with sterile Milli-Q water three times to dislodge weekly bound cells, and then moved to sterile Petri dishes in order to assay bacterial adhesion on thiol surfaces.
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