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. 2013 May 15;41(13):6609–6617. doi: 10.1093/nar/gkt404

Table 1.

Characterization of AAV vector produced by triple plasmid transfection and vaccinia carrier

Production methods 3plasmids VV
Genome titer (qPCR, GC) 2.3 × 1012 2.1 × 1012
Genomic titer (Southern blot, GC) 5.6 × 1012 3.5 × 1012
Capsid titer (Silver staining, pts) 5.0 × 1012 2.5 × 1012
Transduction titer (flow cytometry, TU) 2.5 × 109 2.3 × 109
GC (Southern)/TU ratio 2.2 × 103 1.5 × 103
Ad helper DNA contamination (measured by qPCR) 0.034% 0.024%
AAV helper DNA contamination (measured by qPCR) 0.11% 0.0046%

AAV-CMV-EGFP vector was produced in HEK293 cells by triple plasmid transfection (3plasmids) or was produced in HeLa S3 cells infected with Ad-AAV hybrid virus and vaccinia helper viruses (VV). TU, transducing unit; GC, genome copy; Pts, particles.