大肠杆菌
融合蛋白
生物
基因
克隆(编程)
病毒学
分子生物学
表位
表达式向量
基因表达
病毒
核糖核酸
抗体
重组DNA
遗传学
程序设计语言
计算机科学
作者
Swee Tin Ong,Wen Siang Tan,Sharifah Syed Hassan,Mohd Azmi Mohd Lila,Khatijah Yusoff
标识
DOI:10.1080/1025814021000013994
摘要
The coding region of the nucleocapsid (N) gene was amplified from the viral RNA and inserted into the bacterial expression vector, pTrcHis2, for intracellular expression in three Escherichia coli strains: TOP 10, BL 21 and SG 935. The N protein was expressed as a fusion protein containing the myc epitope and His-tag at its C-terminal end. The amount of the fusion protein expressed in strain SG 935 was significantly higher than the other two strains, and was detected by the anti-myc antibody, anti-His and swine anti-NiV serum. Hence, the N(fus) protein produced in E. coli could serve as an alternative antigen for the detection of anti-NiV in swine.
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