摘要
目的为研究骨缺损的基因治疗提供实验基础,构建人骨形态发生蛋白2真核表达载体。方法采用双酶切方法克隆载体将骨形态发生蛋白2基因与真核表达载体pcDNA3.1连接,构建pcDNA3.1-BMP2表达基因载体。结果通过测序分析证实,成功构建BMP2真核表达载体。结论成功构建BMP2表达载体。
Objective To clone and construct mammal expression vector for human bone morphogenetic protein 2 (BMP2),in order to study gene .therapy for bone defect disease.Methods Plasmid pSPBMP2 was digested by Xba Ⅰ and Sal Ⅰ , the BMP2 gene was subcloned into pcDNA3.1. Results The mammal expression plasmid for BMP2, pcDNA3.1-BMP2, had been constructed. The cloned DNA BMP2 gene was confirmed by sequencing. Conclusion The mammal expression plasmid for BMP2 had been successfully constructed.
出处
《哈尔滨医科大学学报》
CAS
北大核心
2007年第6期524-526,共3页
Journal of Harbin Medical University
基金
黑龙江科技攻关项目(GB01C123-01)