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As a simulation progresses the template reflects more and more a biased overlay between the templates determined by the output activation of the template units.
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Single forward and reverse PCR primers were selected with full complementarity to the template determined by sequence analysis.
Amplification of Vpr from a non-infectious clone, pBKBH10S, was performed using single forward and reverse primers complimentary to the template determined by sequence analysis.
The amount of carbon templates was determined by 5 wt% weight ratios of those to theoretical yield of SAPO-11.
The concentration of templates was determined by qPCR with Library Quantification Kits from KAPA biosystems.
The wetting behaviour of the templates is determined by the hydrophilicity of the surface, the wetting properties of the solution and the contained nanoparticles.
Steady-state kinetic parameters for incorporation of the nucleotide opposite the unmodified and FAF- or FABP-modified templates were determined by following the procedures reported previously.
The linear range of PCR templates was determined by performing a 10-fold serial dilution standard curve, which usually proved a 1 10 dilution was sufficient.
The copy number of rDNA operons of targeted bacteria in crude DNA templates was determined by comparison with serially-diluted plasmid DNA standards run on the same plate.
To determine the efficiency of dCTP insertion opposite the adducted site, steady-state kinetic parameters for incorporation of the nucleotide opposite the unmodified and FABP-modified templates were determined by using the reported literature procedures.
Through providing the various driving potentials from −25 V, −10 V, −5 V to −2.5 V, the different mechanism of electrophoretically depositing ZnO nanoparticles into the colloidal crystal template was determined by the SEM observation of the filled templates.
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