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qRT-PCR reactions using the cDNA as a template revealed a shift in the amplification curve between reactions using either the native luc or synthetic luc* primer pairs.
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It is also worth noting that the effect of target sequence on Ct differed slightly between reactions using the two dyes.
The catalysts A3, A4, and A5 might also be at their maximum activity limit regarding their capability for biodiesel production in this conditions as reported by Montero et al. on MgO nanocrystals [75], since the yields are similar between the reactions using the catalysts A3, A4, and A5.
In any event, the differences between the reactions using pEndos or pCDKS substrates are so pronounced that any variations within the ranges shown in Table 1 are ultimately inconsequential to the models presented below.
The GPR component models the dependency between genes and reactions using Boolean functions usually called gene-protein-reaction (GPR) associations [ 22]).
Special attention was paid on the most significant components of genome-scale network, the gene-protein-reaction (GPR) associations which details the relationships between genes, proteins and reactions using the Boolean logical representations (AND and OR operators).
These are described in Supplementary Tables 1 and 2. The pathway encoded in pLM495 was initially assembled using VEGAS (versatile genetic assembly system)19, and loxPsym sites were subsequently introduced between each pathway gene through PCR reactions using primers that introduced loxPsym sites and terminal, inward pointing BsaI sites.
These loci were screened for allele size polymorphism and genotyped in multiplex PCR of between two and four loci per reaction, using a commercial kit (PCR Multiplex Kit using Q Solution; QIAGEN, Hilden, Germany).
However, it is extremely difficult to differentiate between malignancy and a sarcoid reaction using CT or FDG PET-CT because the tissue involved in the sarcoid reaction accumulates FDG.
Starting from the cleaved structure, we investigated the hydrogen abstraction reaction using the distance between the C5′ atom and the nearest H1° atom on the substrate as reaction coordinate.
Each labelling reaction used between 100 and 250 ng of this LMW RNA as outlined in the methods section.
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