摘要
以日本血吸虫成虫RNA为模板逆转录合成cDNA链,设计合成引物,用PCR法扩增谷胱甘肽转移酶(GST) 基因编码序列,将其克隆入pGEM—T载体,并进行初步鉴定。pGEM—T—GST克隆载体的成功构建,为进一步选择在不同表达系统中表达GST及其在血吸虫病免疫诊断。
SjcDNA first strand synthesis was driven by superscript Ⅱ RT using adult worm RNA as template.Specific primers was designed and synthesized.Coding region gene of SjGST was amplified by PCR.The product from PCR was cloned into pGEM-T-GST vector.The cloning vector pGEM-T-GST was identified by restriction analysis and PCR.The results demonstrated that pGEM-T-GST was successfully constructed and provided the basis for further study on GST expression and its immunological diagnosis and prevention.
出处
《生物学杂志》
CAS
CSCD
1999年第5期11-12,共2页
Journal of Biology
基金
安徽省自然科学基金
关键词
日本血吸虫
谷胱甘肽
转移酶
基因克隆
Schistosoma japincum
Glutathione-s-Transterase
Gene cloning