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In vitro release kinetics were determined for each preparation.
The statement of directions and precautions, the bibliography for each preparation, and the printing of text and formulae are all admirable and remarkably free from errors.
While the use of these organic solvents is not new in the electrochemistry of silicon [2, 3, 8, 12, 13], in this work, we used only newly prepared electrolyte to perform the experiments, and the volume of the organic solvents used for each preparation was the same (190 ml) for all the experiments, ensuring comparable residual contents of water.
The size distribution profiles for each preparation in EMEM/S- at each time point are represented in Figure 6, which shows an increasing tendency of agglomeration for all the AuNPs, except Au[(Gly-Tyr-TrCys)2B], which remained stable over time.
Usually, 4 embryos were used for each preparation.
Two μg of total RNA was used for each preparation of cDNA.
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Patients were maintained on each preparation for 14 days and then switched to the comparator preparation.
Where possible, two to three non-overlapping axons were selected for lesion in each preparation (Fig. 3).
Sixteen cows (237 ± 11 d in milk for H; 213 ± 10 d in milk for L; mean ± SD) were used for each insulin preparation, resulting in n = 4 for each dose within insulin preparation.
Triplicate sample preparations were done on each sample, and two separate HPLC injections were carried out for each replicate preparation.
For each IgG preparation, the isotopic subclass was also determined.
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