Wirth M, Grannemann R, Klehr D, Hauser H
GBF-Gesellschaft für Biotechnologische Forschung mbH, Genetics of Eukaryotes, Braunschweig, Germany.
J Virol. 1994 Jan;68(1):566-9. doi: 10.1128/JVI.68.1.566-569.1994.
To facilitate the screening for clones of transfected packaging cells producing a high yield of recombinant retrovirus, we present a fast and simple method for the isolation of overexpressing cells. By this method the efficiency of virus production can generally be enhanced 10- to 100-fold by application of high selection pressure. Cell lines which exhibit titers of up to 10(8) CFU/ml were obtained.
为便于筛选产生高产量重组逆转录病毒的转染包装细胞克隆,我们提出了一种快速简便的过表达细胞分离方法。通过这种方法,施加高选择压力通常可使病毒产生效率提高10至100倍。获得了滴度高达10(8) CFU/ml的细胞系。