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- W2350139185 abstract "A 0.45 kb DNA fragment containing the 26S promoter of Semliki Forest virus(SFV) and a linker was amplified by PCR and inserted into the multiple clone sites of pSCA1,a suicidal DNA vaccine vector based on SFV replicon,resulting in a modified vector pSCA2 to drive the co-expression of double genes.To further study the expression ability and characterization of the modified expression vector pSCA2,two reporter genes,EGFP and DsRed2,were amplified by PCR and then inserted into the pSCA2,downstream of two 26S promoters respectively,to generate the expression plasmid pSCA2-EGFP/RFP.pSCA2-EGFP/RFP was further transfected into BHK-21 cells.24 h post transfection,green fluorescence and red fluorescence could be observed in all transfected cells using fluorescence microscopy,indicating that the modified expression vector could correctly express two heterologous proteins at the same time.The successful modification of the expression vector pSCA2 offered a useful tool for development of the suicidal DNA vaccine against various pathogens." @default.
- W2350139185 created "2016-06-24" @default.
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- W2350139185 date "2006-01-01" @default.
- W2350139185 modified "2023-09-28" @default.
- W2350139185 title "Construction and Property in Vitro of a Suicidal DNA Vaccine Vector Co-expressing Two Genes" @default.
- W2350139185 hasPublicationYear "2006" @default.
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