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微小隐孢子虫Cp735基因的克隆及原核表达

范大为 肖丹 张西臣 官鹏涛 杨举 李建华

吉林农业大学学报2011,Vol.33Issue(5):567-570,4.
吉林农业大学学报2011,Vol.33Issue(5):567-570,4.DOI:22-1100/S.20110712.0929.002

微小隐孢子虫Cp735基因的克隆及原核表达

Cloning and Prokaryotic Expression of Cp735 Gene of Cryptosporidium parvum

范大为 1肖丹 1张西臣 1官鹏涛 1杨举 1李建华1

作者信息

  • 1. 吉林大学畜牧兽医学院,长春130062
  • 折叠

摘要

Abstract

The Cp735 gene was amplified by PCR. Coding sequence identified by DNA sequencing was cloned into the expression vector pET-28a to construct prokaryotic expression vector. The recombinant protein was expressed in BL21 (DE3) . The result of SDS - PAGE showed that the molecular weight of the expressed product was identical to that of prediction. The result of Western blot demonstrated that the expressed protein had reactogenicity.

关键词

微小隐孢子虫/Cp735基因/克隆/原核表达

Key words

Cryptosporidium parvum/ Cp735 gene/ cloning/ prokaryotic expression

分类

农业科技

引用本文复制引用

范大为,肖丹,张西臣,官鹏涛,杨举,李建华..微小隐孢子虫Cp735基因的克隆及原核表达[J].吉林农业大学学报,2011,33(5):567-570,4.

基金项目

国家科技支撑计划项目(2007BAD40B05),国家传染病防治重大专项(2008ZX10004-001-B) (2007BAD40B05)

吉林农业大学学报

OA北大核心CSCDCSTPCD

1000-5684

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