Exact(7)
The particle sizes were confirmed using a Zetasizer Nano-ZS (Malvern Instruments, Malvern, UK).
Melting temperatures for individual amplicons were determined, and proper PCR product sizes were confirmed using agarose gel electrophoresis.
Amplification was carried out in a DNA thermal cycler (MJ Mini Gradient Thermal Cycler, Bio-Rad Lab, California) and expected fragment sizes were confirmed using gel electrophoresis (2% agarose).
The particle sizes were confirmed using DLS and disk centrifuge techniques.
Following recommended protocols, the cDNA was purified and the sizes were confirmed using 2% agarose electrophoresis.
Library sizes were confirmed using Caliper GX (Perkin Elmer, Waltham, MA), and quantified by qPCR using the Kapa Biosystems quantification kit (Wilmington, MA).
Similar(53)
The age and size were confirmed using publicly available data.
Amplicons of the predicted size were confirmed using agarose gel electrophoresis.
The nucleating effect of CNTs which increased the number of nucleation sites and decreased the average spherulite size was confirmed using polarized optical microscopy.
SMRTbell™ libraries were quantified using the Qubit assay and library size was confirmed using the bioanalyser 12000 kit.
Following amplification, amplicon size was confirmed using the bioanalyser 12000 kit (Agilent, CA, USA) and the concentration confirmed by Qubit assay (Life Technologies, CA, USA).
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