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It is shown that trace amounts of target gas species can be made detectable by adding controlled amounts of known carrier gas.
The interfacial characteristics of emulsion droplets initially coated by Tween 20 could be made either negative or positive (without altering droplet size) by adding controlled amounts of either anionic emulsifiers (SDS) or cationic emulsifiers (DTAB or β-lactoglobulin) to the continuous phase after homogenisation.
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In the case of double transfection, the same total amount of siRNA was used by adding control siRNA to the single siRNA of interest.
The total amount of transfected DNA in any single experiment was kept constant by adding control vector (pcDNA3).
The total amount of plasmid in each transfection was kept constant (400 ng for each well of a 24-well plate) by adding control plasmid.
In all experiments, ( {a}_{{mathrm{H}}_2mathrm{O}} ) was controlled by adding variable amounts of NaCl powder and distilled H2O.
In this case, the composition, size, as well as the surface plasmon resonance of AuAg NPs, can be easily controlled by adding different amounts of hexadecylamine (HDA).
The pH of solution was controlled by adding proper amounts of NaOH, HCl with background electrolyte solution of KCl.
The control is performed by adding varying amounts of oxygen gas to the discharge region using the Plasma Emission Monitor PEM®05.
By adding equal amounts of ENO1-mRNA and control-mRNA (EGFP) to the cells, the number of viable cells in the cell culture was decreased by 80% two days after transfection in the ENO1-mRNA-experiment.
In DFLCA, the increase in the spatial reuse is achieved by adding certain amount of control overhead.
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