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. 2003 Apr;77(8):4528–4538. doi: 10.1128/JVI.77.8.4528-4538.2003

FIG. 3.

FIG. 3.

RT-PCR analysis of recombinant mFIPV. RT-PCR was used to amplify the FIPV-MF S boundaries with RNA isolated from cells infected with mFIPV as a template. (A) Physical map of the genome of the mFIPV recombinant. The dotted area indicates the MF-S gene. The location of the primers used is indicated with an arrow, together with the expected size of the PCR products. (B) RT-PCR with primers PR1254 and PR1255. (C) RT-PCR with primers PR-990 and PR311. See Table 1 for primer sequences. Lanes −RT, no reverse transcriptase added; lanes +RT, reverse transcriptase added; lanes H2O, H2O replacing the template; lanes Contr., pBRDI2 used as a template.