摘要
目的 :构建携带CD基因和LacZ报告基因的腺病毒载体。方法 :先将真核表达载体质粒 pCI中的转录框架构建入腺病毒载体中 ,后再将CD和LacZ基因分别装配到框架的多克隆位点内。结果 :经过酶切鉴定成功地构建了分别携带CD基因和LacZ报告基因的腺病毒载体 ,对肿瘤的前药转换基因治疗有重要意义。
Objective: To construct adenovirus vectors carrying CD gene and LacZ gene. Methods: The open reading frame was released from eukaryonic expression vector plasmid pCI and inserted into the adenovirus shuttle vectors p△E 1 SP1A. Then CD and LacZ genes were put into the polylinker site of the open reading frame in the modified adenovirus vectors respectively. Results: The structure of the adenovirus vectors carrying CD gene and LacZ gene was identified by restriction enzyme analysis. The newly constructed adenovirus is useful for prodrug transformation gene therapy.
出处
《海军医学杂志》
1999年第2期132-135,共4页
Journal of Navy Medicine
基金
国家自然科学基金!批准号 :3 96 0 0 172