摘要
将猪繁殖与呼吸综合征病毒(PRRSV)长春分离株的ORF5基因克隆至真核表达载体pIRES的CMV的启动子下游,并用猪二型圆环病毒的内蒙古分离株的ORF2基因替代pIRES的neo基因,构建真核表达质粒。通过West-ernblot以及IFA检测方法鉴定,所构建的重组质粒能在BHK细胞内进行有效的转录,并表达了目的蛋白。
In this study, ORF5 gene of the changchun PRRSV strain was cloned into pIRES expressing vector , ORF2 gene of the Mongolia PCV2 strain substitute neo gene of pIRES expressing vector.The recombinant DNA vaccine was transcribed and expressed in BHK cells effectively through Western blot and IFA.
出处
《中国动物检疫》
CAS
2010年第3期41-43,共3页
China Animal Health Inspection