专利 已申请

METHOD FOR PREPARING VIRUS-LIKE PARTICLES USING A PROKARYOTIC EXPRESSION SYSTEM

专利「METHOD FOR PREPARING VIRUS-LIKE PARTICLES USING A PROKARYOTIC EXPRESSION SYSTEM」由 Lanzhou Veterinary Research Institute Chinese Academy of Agriculture Sciences 持有,当前状态为已申请,申请号 P/896。LaoBiz 老商通提供老挝知识产权信息检索与企业关联查询。

Patent “METHOD FOR PREPARING VIRUS-LIKE PARTICLES USING A PROKARYOTIC EXPRESSION SYSTEM” is held by Lanzhou Veterinary Research Institute Chinese Academy of Agriculture Sciences; status: 已申请. Search Laos IP records on LaoBiz.

申请号 P/896
申请日期 2023-06-05
申请人 Lanzhou Veterinary Research Institute Chinese Academy of Agriculture Sciences
代理机构 CONCETTI-LAO CO., LTD
类别 C12N 7/00

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基础信息

类型
专利
申请号
P/896
状态
已申请
申请人
Lanzhou Veterinary Research Institute Chinese Academy of Agriculture Sciences
代理机构
CONCETTI-LAO CO., LTD
申请日期
2023-06-05
公开/公告日
2026-04-03
国际分类
C12N 7/00
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摘要

A method for preparing virus-like particles through a prokaryotic expression system comprises: l) inoculation;2) bacteria culture: 2.1) adding a carbon source culture medium to a batch culture medium to maintain the pH of the bacteria suspension within a range of 6.95- 7.05; where the carbon source culture medium comprises a carbon source and an ammonium salt of strong acid; and2.2) adding a nitrogen source culture medium to the batch culture medium when the bacteria suspension reaches an OD600 of 7-10; 3) low-temperature culture; 4) induction expression of protein; and 5) purification and assembly. The method employs E. coli prokaryotic expression system as a carrier, and performs fed-batch culture by adding the nitrogen source and the carbon soruce in a C/N ratio at a feed rate, thus increasing the growth of the E. coli.

A method for preparing virus-like particles through a prokaryotic expression system comprises: l) inoculation;2) bacteria culture: 2.1) adding a carbon source culture medium to a batch culture medium to maintain the pH of the bacteria suspension within a range of 6.95- 7.05; where the carbon source culture medium comprises a carbon source and an ammonium salt of strong acid; and2.2) adding a nitrogen source culture medium to the batch culture medium when the bacteria suspension reaches an OD600 of 7-10; 3) low-temperature culture; 4) induction expression of protein; and 5) purification and assembly. The method employs E. coli prokaryotic expression system as a carrier, and performs fed-batch culture by adding the nitrogen source and the carbon soruce in a C/N ratio at a feed rate, thus increasing the growth of the E. coli.

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