摘要
以人免疫缺陷病毒2( H I V2) 的原病毒基因组为模板,通过套式 P C R 扩增得到了 H I V2 的一段特异性膜抗原蛋白基因片段;随后将此片段克隆入诱导表达载体p G E X5 X1 ,获得了重组表达质粒p G E X36 E N V. I P T G 对重组表达菌株诱导后, S D S P A G E
A DNA fragment coding for a dominant epitope of the transmembrane region from Human Immunodeficiency Virus2(HIV 2) Proviral genome was amplified by nested PCR,which was directly cloned into pGEM R T vector.The following enzymatic analysis primarily verified the amplified product.The DNA fragment was then inserted into pGEX 5X 1 expression plasmid and the recombinant plasmid pGEX36 ENV wsa transformed into E.coli.The result of SDS PAGE analysis showed that a new protein band corresponding to the fusion form between GST and the objective peptide was produced.
出处
《山东大学学报(自然科学版)》
CSCD
1999年第3期347-351,共5页
Journal of Shandong University(Natural Science Edition)
关键词
免疫缺陷病毒
穿膜蛋白
克隆
表达
基因表达
HIV 2,nested PCR
transmembrane protein gene
cloning and expression