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Different acids were used for the carbon nanotube (CNT) purification.
After trimming the saturated sites and poorly aligned regions in the concatenated alignment, 2,128,000 amino acids were used for the phylogenomic analysis.
Trace-metal grade acids were used for pH adjustments and acid-cleaning of containers.
Accordingly, the rutile phase was obtained when sulfuric and nitric acids were used for the peptization.
Thus, the same acids were used for separation of foil coatings of varying chemistries which depended on the supplier.
Boronic acids were used for the direct immobilisation of proteins by the interaction with the glycosylated part of the protein structure [90]-[92 [90]-[92eans of immobilisation of their particular coenzymes [93],[94] for their detection or for the detection of other analytes.
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Note that the method of evaluating the free amino acids was used for all subsequent procedures.
SC medium lacking particular amino acids was used for auxotrophic marker selection.
The organic phase (acyl methyl estered fatty acids) was used for GC analysis.
For the production of 2D MoO3 nanosheets, the precursor consisting of molybdate salt and organic aliphatic acids is used for hydrothermal synthesis [74].
Some ingested amino acids are used for protein biosynthesis, while others are converted to glucose through gluconeogenesis, or fed into the citric acid cycle.
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