摘要
本研究通过RT-PCR扩增了猪流感病毒A/Swine/Inner Mongolia/547/01(H3N2)的NP基因,并将其克隆入pMD18-T载体。重组pMD18-T经SalI和EcoR I酶切后得到的NP基因插入pMelBacB载体的SalI/EcoRI位点。PCR和限制性内切酶分析鉴定表明成功构建了pMelBacB-NP转移载体。这为开发NP诊断抗原和亚单位疫苗奠定了基础。
In the study,NP gene of A/ Swine/ Inner Mongolia/ 547/ 01 (H3N2)was amplified by RT-PCR.The product of RT-PCR was cloned into pMD 18-T vector.NP gene was inserted into the Sal I/EcoR I sites of pMelBacB after the recombinant pMD18-T was cleavaged with restriction endonuclease Sal I and EcoR I.Identification by PCR and restriction-endonuclease analysis showed that the recombinant transfer vector pMelBacB-NP was constructed successfully.It was helpful for development of diagnostic antigen and subunit vaccine based on NP
出处
《西南农业学报》
CSCD
北大核心
2009年第5期1453-1455,共3页
Southwest China Journal of Agricultural Sciences
关键词
猪流感病毒
NP基因
克隆
转移载体
Swine influenza virus
NP gene
Cloning
Transfer vector