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Fig. 1 | Virology Journal

Fig. 1

From: Design of a chimaeric antigen and its use in the detection of IgG antibodies against rubella virus

Fig. 1

Agarose gel electrophoresis of P6T and its expression vector after double digestion. The target fragment P6T linked to PGEM-T and the expression vector PET-32a (+) were digested with restriction enzymes BamHI and HindIII, and the obtained target fragment was recovered for identification by agron gel electrophoresis. 1: DNA marker, DL2000; 2: P6T plasmid; 3: double restriction enzyme (BamHI, HindIII) digestion product of pET-32a (+)

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