摘要
为建立一种简便可行的检测HBV前C区1896位G→A突变的方法。采用本室自行构建的HBV前C区1896位G→A突变株和野生株克隆作为标准株,对错配引物PCR(mp-PCR)结合限制性片段长度多态性分析(RFLP),作为检测HBV前C区1896位G→A突变株的方法进行了评价。结果显示,该方法操作较为简便,特异性和重复性均较满意。
For establishing a practical detection method of HBV precore 1896nt mutant, HBV precore 1896nt G>A mutant and wild clones constructed by our department as standard strains combined the mispairedPCR (mpPCR) with restricted fraction length polymorphism (RFLP) were used to detect HBV precore 1896nt mutant. The results show that the method is satisfied in specificity and repeatability with simpler procedure. It may be applied in clinical practice and research work.
出处
《南京医科大学学报(自然科学版)》
CAS
CSCD
1998年第3期178-181,共4页
Journal of Nanjing Medical University(Natural Sciences)
基金
江苏省教委自然科学基金
关键词
乙型肝炎病毒
前C区
突变株
基因克隆
PCR
HBV precore mutant
gene clone
mispairedPCR
restrict fraction length polymorphism