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Modification,Expression and Purification of Human Endotoxin Binding Peptide Gene / 中国生物工程杂志
Article en Zh | WPRIM | ID: wpr-684886
Biblioteca responsable: WPRO
ABSTRACT
Objective: To modify EBP(endotoxin binding peptide), clone and express the mutate of EBP gene and gain purified mEBP.Method: mEBPgene was cloned by PCR site-directed mutagenesis. PinpointXa-3/mEBP expression vector was designed to express human mEBP as a fusion protein in BL21 (DE3) pLysS. Digested engineering bacteria by lysozyme and collected inclusion bodies.Fusion protein was purified by Pinpoint TM Xa purification system and cleaved by factorXa,mEBP was purified by RP-HPLC. Results: Mutations at residues 5 and 18(Gln→Lys) was obtained by PCR site-directed mutagenesis, expressed and purified mEBP successfully.Conclusions: Obtaining of purified mEBP lay a foundation for its biological activity research.
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Texto completo: 1 Índice: WPRIM Idioma: Zh Revista: China Biotechnology Año: 2006 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Idioma: Zh Revista: China Biotechnology Año: 2006 Tipo del documento: Article