Vectors bicistronically linking a gene of interest to the SV40 large T antigen in combination with the SV40 origin of replication enhance transient protein expression and luciferase reporter activity

BioTechniques

Volumn 51, Issue 2, 2011, Pages 119-126

  Mahon, Matthew J ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

catenin; IRES; Luciferase; Mammalian two hybrid; SV40 large T antigen

Indexed keywords

BETA CATENIN; LUCIFERASE; PLASMID VECTOR; RED FLUORESCENT PROTEIN; T CELL FACTOR PROTEIN; VIRUS LARGE T ANTIGEN; VIRUS VECTOR;

ANIMAL CELL; ARTICLE; CISTRON; CONTROLLED STUDY; EXPRESSION VECTOR; FLUORESCENCE; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; INTERNAL RIBOSOME ENTRY SITE; NONHUMAN; POSITIVE FEEDBACK; REPORTER GENE; SIMIAN VIRUS 40; VIRUS REPLICATION;

ANTIGENS, POLYOMAVIRUS TRANSFORMING; CLONING, MOLECULAR; FEEDBACK, PHYSIOLOGICAL; GENE EXPRESSION; GENES, REPORTER; GENES, VIRAL; GENETIC VECTORS; HEK293 CELLS; HUMANS; LUCIFERASES; MICROSCOPY, CONFOCAL; RECOMBINANT PROTEINS; REPLICATION ORIGIN; SIMIAN VIRUS 40; TWO-HYBRID SYSTEM TECHNIQUES;

MAMMALIA; SIMIAN VIRUS 40;

EID: 80051563662     PISSN: 07366205     EISSN: 19409818     Source Type: Journal    
DOI: 10.2144/000113720     Document Type: Article

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