摘要
从鸡贫血病毒(CAV———ch icken anem ia virus)总DNA中克隆凋亡蛋白(Apoptin)基因片段,并与pcDNA3.1/CT-GFP-TOPO载体构建融合载体,转化E.coli.DH5α,筛选氨苄抗性阳性克隆并鉴定.以该融合载体转染Hep2细胞后,在倒置荧光显微镜下观察到绿色荧光标记,同时观察到细胞核形态学呈凋亡特征变化,表明凋亡蛋白可以诱导Hep2细胞系发生凋亡.
The pcDNA3.1/CT- GFP- Apoptin- TOPO was reconstructed with apoptin gene cloned from all DNA of chicken anemia virus. The anti-ampicillin cloney was selected after transforming into E. coli DH5α, then the plasmid was verified and purified. Hep2 cell lines were transfected by the fusion vectors, and GFP marker was observed by inverted fluorescence microscope. Subseq as exclusive apoptotic description. Theses implied that Hep2 uently, the morphology was changed as same lines were apoptosis induced by apoptin.
出处
《哈尔滨工业大学学报》
EI
CAS
CSCD
北大核心
2005年第8期1066-1067,1073,共3页
Journal of Harbin Institute of Technology
基金
黑龙江省自然科学基金资助项目(C203)