Figure 5个  Table 4
    • Table 1.  Oligonucleotide sequence and orientation of primers designed for PCR amplification of TrIV putative ORFs from a cDNA library

    • Table 2.  Oligonucleotide sequence and orientation of primers designed for quantitative real-time RT-PCR (qPCR) amplification of TrIV putative ORFs.

    • Table 3.  Overall assessment of the expression (detected or not; + or -) of known and predicted TrIV ORFs in TrIV-infected C. fumiferana larvae.

    • Table 4.  Differences between predicted and observed splicing junctions for two TrIV spliced genes, TrV3 and a Cys-motif gene.