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The IRa section was subsequently added manually to the contig, and IR boundaries were confirmed using PCR.
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The single-copy IR boundary regions were confirmed using region-specific primer pairs.
These observations were confirmed using pharmacologic inhibitors.
Results were confirmed using qPCR analysis.
The genomic equine consensus sequence was confirmed using data from the Equine Genome Sequencing Project (2x) [ 38] and intron/exon boundaries were assigned by local alignment to the full-length equine OAS1 [GenBank: AY321355] and RNASEL [GenBank: DQ497159] cDNAs.
This was confirmed using TBR1 null mice.
Convergence was confirmed using AWTY [67].
Protein purity was confirmed using SDS-PAGE.
Equal loading was confirmed using β-actin.
Functionalization was confirmed using fluorescent GRGDSPC peptides.
Staging was confirmed using embryo morphology [48].
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