Development of efficient method for purified recombinant bovine granulocyte-macrophage colony-stimulating factor production with baculovirus-silkworm gene expression system
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作者:
Nagaya, Hidekazu
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机构:Katakura Ind Co Ltd, Sayama, Saitama 3501332, Japan
Nagaya, Hidekazu
Kanaya, Toshimichi
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机构:Katakura Ind Co Ltd, Sayama, Saitama 3501332, Japan
Kanaya, Toshimichi
Tobita, Yoneko
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机构:Katakura Ind Co Ltd, Sayama, Saitama 3501332, Japan
Tobita, Yoneko
Yokomizo, Yuichi
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机构:Katakura Ind Co Ltd, Sayama, Saitama 3501332, Japan
Yokomizo, Yuichi
Inumaru, Shigeki
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机构:Katakura Ind Co Ltd, Sayama, Saitama 3501332, Japan
Inumaru, Shigeki
Onodera, Takashi
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机构:Katakura Ind Co Ltd, Sayama, Saitama 3501332, Japan
Onodera, Takashi
机构:
[1] Katakura Ind Co Ltd, Sayama, Saitama 3501332, Japan
[2] Kitayama Labes Co Ltd, Nagano 3994431, Japan
[3] Natl Inst Anim Hlth, Tsukuba, Ibaraki 3050856, Japan
[4] Univ Tokyo, Dept Mol Immunol, Sch Agr & Life Sci, Bunkyo Ku, Tokyo 1138657, Japan
Recombinant bovine granulocyte-macrophage colony-stimulating factor (rboGM-CSF) was produced by the baculovirus-silkworm expression system. It was purified to 98% by (NH4)(2)SO4, followed by a three-step column chromatography with silica gel, ion exchange resin and a metal chelate column. The specific activity of purified rboGM-CSF was 1.6-6.3 10(6) ED50 mg(-1). By this method, the specific activity was raised 160-fold and 21% of the expressed rboGM-CSF was recovered.