Expression vector system based on the chicken β-actin promoter directs efficient production of interleukin-5

Gene

Volumn 79, Issue 2, 1989, Pages 269-277

  Jun ichi, Miyazaki ^a   Satoshi, Takaki ^a   Kimi, Araki ^a   Fumi, Tashiro ^a   Akira, Tominaga ^a   Kiyoshi, Takatsu ^b   Ken ichi, Yamamura ^a  

^a KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

^b Institute for Medical Immunology Kumamoto University Medical School ^*

Author keywords

DNA replication; DNA transfection; promoter activity; Recombinant DNA; splicing; SV40 T antigen; transient expression; galactosidase assay

Indexed keywords

BETA ACTIN; BETA GALACTOSIDASE; INTERLEUKIN 5; RADIOISOTOPE; RECOMBINANT DNA;

ANIMAL CELL; CELL CULTURE; CHICKEN; GENETIC ENGINEERING; HEREDITY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROMOTER REGION; RNA SPLICING; ROUS SARCOMA ONCOVIRUS; SIMIAN VIRUS 40;

ACTINS; ANIMAL; BETA-GALACTOSIDASE; CELLS, CULTURED; CHICKENS; CHROMATOGRAPHY, AFFINITY; CLONING, MOLECULAR; ELECTROPHORESIS, POLYACRYLAMIDE GEL; ESCHERICHIA COLI; GENETIC VECTORS; INTERLEUKIN-5; LAC OPERON; NUCLEOTIDE MAPPING; PLASMIDS; PROMOTER REGIONS (GENETICS); SIMIAN VIRUS 40; TRANSFECTION;

EID: 0024362504     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/0378-1119(89)90209-6     Document Type: Article

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