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A two-plasmid system for transient expression of cDNAs in primate cells.

作者信息

Asselbergs F A, Grand P

机构信息

Biotechnology Department, Ciba-Geigy Ltd., Basel, Switzerland.

出版信息

Anal Biochem. 1993 Mar;209(2):327-31. doi: 10.1006/abio.1993.1128.

DOI:10.1006/abio.1993.1128
PMID:8385892
Abstract

This two-plasmid system for transient gene expression can be used in a wide variety of primate cells. It consists of a cDNA expression vector and a helper plasmid. The cDNA cloned in the expression vector is transcribed by the powerful major immediate-early promoter of murine cytomegalovirus. A segment of the rabbit beta-globin gene placed downstream of the cDNA provides signals for splicing and polyadenylation. The helper plasmid provides SV40 T antigen and adenovirus VA RNA. The T antigen induces replication of the expression vector, which contains an SV40 origin of replication, and VA RNA enhances translation of the transcribed mRNA. In monkey kidney cells, with human tissue-type plasminogen activator (t-PA) cDNA as reporter gene, the helper plasmid boosted t-PA production 30-fold and up to 500 ng/ml t-PA accumulated in the medium in the 5 days following transfection of the two plasmids. In nonprimate cells the helper plasmid stimulated expression 3- to 5-fold.

摘要

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