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Several constructs were designed against the lamin A/C target.
Specific primers were designed against HHV-6 U86 gene.
Dual-color break-apart probes were designed against the genomic region adjacent to SS18.
Four small interfering RNAs (siRNAs) were designed against unique sequences in the K6a 3′-untranslated 3′-untranslated
Detection primers were designed against the genomic sequences of four viruses.
The capture probes were designed against previously identified and described hotspots for quinolone resistance (codons 83 and 87 of gyrA).
In the first approach, short interfering RNAs were designed against either human aromatase mRNA or human COX-2 mRNA.
Primers and a probe were designed against existing genomic sequences to amplify a 72 bp fragment from RNA-2.
The categories were designed against the background of domain-specific quality standards which were identified during the domain analysis (see Appendix Table 6).
Antisense-morpholino phosphorodiamidate oligonucleotides were designed against following sequences (GeneTools, Philomath, USA).
In addition, multiple probes were designed against long PCR fragments generated from phage Lambda.
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