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AFM was used for analyzing the surface morphology of the samples as well as for determination of the average heights (h QD) and densities (ρ QD) of the QDs.
The ability to synthesize a chiral pharmaceutical intermediate, ABT in relatively short time proves this IEMR system as a powerful tool for construction and evaluation of de novo pathways as well as for determination of enzyme kinetics.
An analysis of the transverse magnetization relaxation function is proposed as a method for melting point determination as well as for determination of the extent of crystallization as a function of time during an isothermal crystallization.
The cultivations were carried out each for three times in triplicates, using two cultures of the triplicate for whole cell biotransformation assays and the third culture for mechanical cell disruption by sonication and subsequent SDS-PAGE analysis as well as for determination of the cell dry weight.
The obtained results may be useful for development and optimization of novel forms of magnetocarried medical remedies of targeted delivery and adsorbents based on nanocomposites of superparamagnetic core shell type with multilevel nanoarchitecture, as well as for determination and control of the size parameters of its components.
The obtained results may be used for the development of novel forms of magnetocarried medical remedies for targeted delivery and adsorbents based on nanocomposites of superparamagnetic core shell type with multilevel nanoarchitecture, as well as for determination, control, and optimization of the size parameters of its components.
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The method achieves extremely low limits of detection (<0.02 μg/L), in both surface and drinking waters and it is used for identification and verification purposes as well as for determinations at the ppt level.
These observations should be taken into account when using fluorescent dyes as probes for determination of transporter activity as a measure of MDR.
Acetate is generally used as substrate for determination of SMA.
Ten patients with anemia served as controls for determination of cytokine levels.
The supernatant obtained was used as enzyme for determination of laccase activity and for the estimation of proteins.
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