摘要
利用套式PCR技术体外扩增蚊体内间日疟原虫SSUrDNA长121bp的特定片段,将此片段克隆到载体PUC18中,转化受体菌株DH5α,测序结果表明,扩增DNA序列与背景序列完全一致,证实为间日疟原虫SSUrDNA目的片段。
The specific SSUrDNA fragments of 121bp from DNA extracted from Plasmodium vivax infected mosquito were amplified in vitro using nested polymerase chain reaction. The products of nested PCR were coloned in SmaI site of PUC18. The result of sequencing showed that the sequence of amplified DNA fragment was indeed SSUrDNA of P.vivax.
出处
《寄生虫与医学昆虫学报》
CAS
1998年第4期235-239,共5页
Acta Parasitologica et Medica Entomologica Sinica