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SEC fraction highlighted in bold was selected for further analysis.
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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).
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.
Note: The genomes which are highlighted in bold were selected for the analysis using 16S rRNA sequences and the phylogenetic tree for these cases is provided in Figure 2.
One successful training regimen (bolded in Table 1) was selected for further testing.
Genes in bold were selected by more than two studies.
A universal set of Primer was selected for this study from the primer database available in BOLD system to target the barcode COI sequence of the Antilope cervicapra.
The genes with black bold ID were selected for qRT-PCR analysis.
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CEO of Professional Science Editing for Scientists @ prosciediting.com