Figure 4.
PCR analysis using the primer combination bcas3, bcas10 and neoint.4 on DNA isolated from representative cell clones derived after electroporation of HM1 RMCE2272-98 cells with the plasmid pShuttle-G5 and selection of the transfected cells in medium containing 200 µg/ml of G418. The 1317-bp band is detected in all samples and represents the unmodified β-casein allele. Cell clones modified by an RMCE event, which has inserted the PGK-neo selection marker cassette, display an additional 1023-bp PCR product. Phage λ DNA digested with HindIII and EcoRI was used as molecular weight marker.