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Expression of cre gene in Escherichia coli and bioassay its expression product / 生物工程学报
Chinese Journal of Biotechnology ; (12): 497-500, 2002.
Artículo en Chino | WPRIM | ID: wpr-256177
ABSTRACT
The Cre recombinase from bacteriophage P1 can recognize specific DNA sequences, cleave DNA at specific target sites, and then ligate it to the cleaved DNA of a second site. In this study, cre gene was cloned into the pGEM-T Easy vector via PCR procedure. Then the cre gene was inserted into an expression vector pET-29a and expressed in E. coli BL21 (DE3). A 38 kD soluble protein was expressed and named CRE. CRE was purified by DEAE-52 chromatography. Bioassay of the partially purified product showed that CRE can cleave the plasmid pGLGFP which contains two loxP site with the same direction.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Plásmidos / Proteínas Virales / Proteínas Recombinantes / Regulación Enzimológica de la Expresión Génica / Cromatografía DEAE-Celulosa / Integrasas / Proteínas Fluorescentes Verdes / Escherichia coli / Genética / Proteínas Luminiscentes Idioma: Chino Revista: Chinese Journal of Biotechnology Año: 2002 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Plásmidos / Proteínas Virales / Proteínas Recombinantes / Regulación Enzimológica de la Expresión Génica / Cromatografía DEAE-Celulosa / Integrasas / Proteínas Fluorescentes Verdes / Escherichia coli / Genética / Proteínas Luminiscentes Idioma: Chino Revista: Chinese Journal of Biotechnology Año: 2002 Tipo del documento: Artículo