I want to use the CMV-Promotor of pcDNA3 in another Vector that
contains a pac gene for selection in CHO-cells (pBEHpac18 (SV40
It would be very easy to clone if I would only cut out the promotor
without the BGH polyA site. I would then use an SV40 polyA site with
the CMV Promotor.
Does anyone know if that would lead to any problems ?
Please send me an E-Mail :
melcher at mathematik.uni-marburg.de
Institut für Physiologische Chemie, Marburg (AG Hasilik)