Modification of the Creator recombination system for proteomics applications - Improved expression by addition of splice sites

BMC Biotechnology

Volumn 6, Issue , 2006, Pages

  Colwill, Karen ^a   Wells, Clark D ^a   Elder, Kelly ^a   Goudreault, Marilyn ^a   Hersi, Kadija ^a   Kulkarni, Sarang ^a   Hardy, W Rod ^a,b   Pawson, Tony ^a,b   Morin, Gregg B ^a,c  

^a MOUNT SINAI HOSPITAL   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c BRITISH COLUMBIA CANCER AGENCY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

GENETIC ENGINEERING; OPTIMIZATION; PROTEINS; VECTORS;

CREATOR RECOMBINATION SYSTEM; GENE FUNCTION ANALYSIS; PROTEOMICS;

BIOTECHNOLOGY;

BETA GALACTOSIDASE; COMPLEMENTARY DNA; CRE RECOMBINASE; DNA; EPITOPE; HYBRID PROTEIN; INTEGRASE; VIRUS PROTEIN;

ARTICLE; ASSAY; EXPRESSION VECTOR; GENE FUNCTION; GENE SEQUENCE; HIGH THROUGHPUT SCREENING; HOMOLOGOUS RECOMBINATION; HUMAN; LOXP SITE; MAMMAL; NONHUMAN; OPEN READING FRAME; PROMOTER REGION; PROTEIN EXPRESSION; PROTEOMICS; REPORTER GENE; RNA SPLICING; CELL LINE; GENE VECTOR; GENETIC RECOMBINATION; GENETICS; METABOLISM; METHODOLOGY; MOLECULAR CLONING;

MAMMALIA;

CELL LINE; CLONING, MOLECULAR; GENETIC VECTORS; HUMANS; INTEGRASES; OPEN READING FRAMES; PROTEOMICS; RECOMBINANT FUSION PROTEINS; RECOMBINATION, GENETIC; RNA SPLICE SITES; RNA SPLICING; VIRAL PROTEINS;

EID: 33645468737     PISSN: 14726750     EISSN: 14726750     Source Type: Journal    
DOI: 10.1186/1472-6750-6-13     Document Type: Article

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