Exact(2)
In total, seven primer pairs have been designed (Table 2).> -wrap-foot> Priners in bold selected as the most specific for the selected region of A. versicolor, yielding an amplicon of 53 base pairs The qPCR assay (Aversi_ITS qPCR method) was performed with the SYBR® green chemistry using a real-time PCR IQ5™ system from Bio-Rad (Temse, Belgium).
In bold: selected models for which ΔDIC > 5, i.e. the model including interaction had a smaller DIC.
Similar(58)
miRNAs selected for validation are represented in bold miRNAs selected for validation are represented in bold The recognition that PC clusters within families has led to the collection of HPC families with the goal of localizing and identifying PC susceptibility genes.
All predictors were used for the regional scale analysis, predictors in bold were selected for the local scale analysis (for more information see Appendix I).
Teams in regular type qualified by virtue of their league finish; teams in bold were selected as at-large teams by a committee today to round out a 16-team field in each division.
SEC fraction highlighted in bold was selected for further analysis.
Genes in bold were selected by more than two studies.
Driver lines shown in bold were selected for more detailed experiments.
Genes highlighted in bold were selected for validation by real time PCR (see Table 6).
*Genes in bold were selected for candidate gene analyses by qRT-PCR.
Genes in bold were selected for candidate gene analyses by qRT-PCR.; # marginal signal intensity; NCBI, National Center for Biotechnology Information GBB, GenBank.
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