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XRD patterns of CIGS nanopore films were shown in Figure 5. Spectra of Au-coated and pure AAO templates were measured for comparison.
Physical interactions among anchor and test primers, in the experimental and control templates, were measured by qPCR (SYBR® Green) and resulting frequencies were calculated and normalised using the XPB/ Eccr3 locus as control [ 61, 62].
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To further investigate the difference in activity between SIL and silibinin, the effect of these mixtures on the ability of purified NS5B RNA polymerase to bind 32P-labeled RNA templates was measured in a filter-binding assay.
The efficacy of extension from these templates was measured by determining the kinetic parameters for incorporation of the next correct nucleotide (dG) to each primer-template combination.
Metal ion (Au III) or Pd II)) loading on the TMV1Cys template was measured as a function of the equilibrium concentration of Au III) or Pd II) ions in solution at several temperatures.
Each template was measured in technical triplicates, and PCR efficiency was between 95 and 100%.
Concordance between genotypes generated from MDA product and gDNA templates, together with the genotype and sample failure rates of each template type were measured.
Amplicon template quantities were measured using a threshold cycle (Ct) method [ 47, 48].
A nanomesh graphene (NMG) was produced by a chemical vapor deposition using porous MgO layers as templates, and its magnetic properties were measured and compared with those of reduced graphene oxide (rGO).
Chr = chromosome The specificity and linearity of the assays were measured using standard templates of known ratios of methylated:unmethylated DNA.
The local flash mfERG implicit times were measured by using a template scaling method [ 18].
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