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This modification is conducted in the assembled microfluidic cell, with minimum material and time consumption.
This modification is conducted by DNA topoisomerases and involves transient cleavage and re-ligation of the double-stranded DNA molecule.
This modification is conducted by DNA topoisomerases and involves transient cleavage of one or both strands of DNA followed by religation of the double helix (Champoux, 2001).
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To improve the specific activity and catalytic efficiency of l-LcLDH1, an NADH-dependent allosteric l-lactate dehydrogenase from L. casei, towards phenylpyruvic acid (PPA), its directed modification was conducted based on the semi-rational design.
To improve the compressibility of low-compressibility saccharides, particle modification was conducted by coating and granulating a low-compressibility saccharide with a high one to enable the production of a fast-disintegrating tablet.
When the modification was conducted in an alkaline (e.g. 0.1 M KOH) solution, in aqueous solutions under applying a potential more positive than 0.3 V vs. Ag/AgCl, or at a low modifier concentration (e.g. 20 μM), the proper 4-PySH modified surface was obtained even using 4-PySH as received, which contained a small amount of sulfide.
Modification was conducted in dry toluene.
The modification was conducted at 37°C for 1 h, each sample containing 10 mL of erythrocyte suspension of 2% hematocrit was stirred continuously.
Experiments on classification performance using these modifications are conducted to demonstrate their feasibility.
During the process of testing for MI, model modifications were conducted post hoc if modification indices matched theoretical justifications.
Thus, as suggested by Jöreskog, several modifications were conducted on the basis of empirical and theoretical-logical rationales.
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