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. 2013 Nov;87(22):12029–12040. doi: 10.1128/JVI.01267-13

Table 1.

Expression plasmids constructed for this studya

Expression plasmid Template plasmid Forward primer Reverse primer
pFUΔss ON-C p44B peL Fe-130S Fe-50R
pFUΔss 44B pON-C Fe-130S Fe-50R
pFUΔss DC6 pCR4 ERV-DC6 Fe-130S Fe-126R
pFUΔss DC8 pCR4 ERV-DC8 Fe-130S Fe-126R
pFUΔss DC14 pCR4 ERV-DC14 Fe-130S Fe-126R
pFUΔss DC19 pCR4 ERV-DC19 Fe-130S Fe-126R
pFUΔss 4070A pCL-Ampho 4070A-2S 4070A-2R
pFUΔss FeLIX pCR-Blunt FeLIX FeLIX-1F FeLIX-1R
pFUΔss 3201-2D pCR-Blunt 3201-2D Fe-207S Fe-190R
pFUΔss 3201-2A pCR-Blunt 3201-2A Fe-209S Fe-187R
a

Each DNA fragment was PCR amplified with the indicated primers and template plasmid and then inserted into the pFUΔss expression vector. Primer sequences are shown in Table 2.