Development of efficient method for purified recombinant bovine granulocyte-macrophage colony-stimulating factor production with baculovirus-silkworm gene expression system

Biotechnology Letters

Volumn 30, Issue 1, 2008, Pages 41-45

  Nagaya, Hidekazu ^a   Kanaya, Toshimichi ^a,b   Tobita, Yoneko ^a   Yokomizo, Yuichi ^c   Inumaru, Shigeki ^c   Onodera, Takashi ^d  

^a Katakura Industries Co Ltd   (Japan)

^b Kitayama Labes Co Ltd   (Japan)

^c NATIONAL INSTITUTE OF ANIMAL HEALTH   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

Baculovirus; Bovine; GM CSF; Purification; Silkworm

Indexed keywords

BIOACTIVITY; COLUMN CHROMATOGRAPHY; PURIFICATION; SILICA GEL; VIRUSES;

BACULOVIRUS; SILKWORM; SPECIFIC ACTIVITY; THREE-STEP COLUMN CHROMATOGRAPHY;

GENE EXPRESSION;

GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; RECOMBINANT PROTEIN;

ANIMAL; ARTICLE; BACULOVIRUS; CATTLE; CHEMISTRY; GENE VECTOR; GENETICS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ION EXCHANGE CHROMATOGRAPHY; ISOLATION AND PURIFICATION; METABOLISM; METHODOLOGY; MOLECULAR CLONING; PROTEIN ENGINEERING; SILKWORM;

ANIMALS; BACULOVIRIDAE; BOMBYX; CATTLE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CHROMATOGRAPHY, ION EXCHANGE; CLONING, MOLECULAR; GENETIC VECTORS; GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR; PROTEIN ENGINEERING; RECOMBINANT PROTEINS;

BOMBYX MORI; BOVINAE;

EID: 36649038525     PISSN: 01415492     EISSN: 15736776     Source Type: Journal    
DOI: 10.1007/s10529-007-9506-3     Document Type: Article

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