RRC ID 28597
著者 Nagahashi K, Umemura K, Kanayama N, Iwaki T.
タイトル Fusion of fluorescent protein to puromycin N-acetyltransferase is useful in Drosophila Schneider S2 cells expressing heterologous proteins.
ジャーナル Cytotechnology
Abstract The Drosophila melanogaster Schneider 2 (S2) cell line was established in 1972. Many studies have indicated that generation of recombinant proteins with S2 cells is more desirable than using other methods, since native proteins derived from S2 cells do not usually interact with those derived from mammalian cells. In order to minimize the duration for selections, we established an all-in-one single plasmid pMT-PURO, which enables to express the gene of interest as well as a selection gene "pac". However, there is a weak point in the system. In order to verify the hallmark of the transformed cells, puromycin selection as well as verification of the gene of interests is still necessary. To improve this situation, we generated pMT-PURO2G and pMT-PURO2R, which enable to verify the hallmark of the transformed cells during the selections by the detection of enhanced green fluorescent protein (EGFP) or DsRED2. This new system gives reliable and reproductive results for recombinant protein synthesis and gets rid of some degree of uncertainty for the outcome of the transfection.
巻・号 65(2)
ページ 173-8
公開日 2013-3-1
DOI 10.1007/s10616-012-9473-y
PMID 22706964
PMC PMC3560874
IF 1.777
引用数 2
WOS 分野 BIOTECHNOLOGY & APPLIED MICROBIOLOGY CELL BIOLOGY
リソース情報
遺伝子材料 pMT-PURO2G (RDB09004) pMT-PURO2R (RDB09005) pMT-PURO2 (RDB12152)