检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]辽宁医学院,辽宁省锦州市121000 [2]辽宁医学院附属第一医院病理科
出 处:《中国全科医学》2013年第12期1342-1345,共4页Chinese General Practice
基 金:辽宁省科技基金项目(2010225034)
摘 要:目的构建携带增强绿色荧光蛋白基因的人14-3-3σ真核表达载体pEGFP-GV142-SFN并转染至人乳腺癌MCF-7细胞,鉴定所表达的蛋白活性。方法通过逆转录-聚合酶链反应从胎脑组织中获得编码14-3-3σ的全长cDNA,定向克隆至真核表达载体GV142中,鉴定正确后与带有增强绿色荧光蛋白的pEGFP-N1-SFN酶切后连接,重组携带14-3-3σ的表达载体pEGFP-GV142-SFN。将pEGFP-GV142-SFN质粒转染至乳腺癌MCF-7细胞,观察荧光蛋白的表达。结果经限制性内切酶酶切分析、聚合酶链反应和DNA序列测定证实目的基因已插入重组质粒,荧光显微镜下观察发现:转染24 h后,乳腺癌MCF-7细胞内可见增强绿色荧光蛋白表达,48 h表达最稳定,72 h可见荧光蛋白淬灭,细胞形态逐渐消失。结论成功构建了14-3-3σ真核表达载体pEGFP-GV142-SFN并转染至乳腺癌MCF-7细胞,观察和检测到绿色荧光蛋白表达。Objective To construct the eukaryotic expression vector of human 14 - 3 - 3σ containing enhanced green fluorescence protein gene and to transfer it into humman breast cancer cell MCF - 7 in order to identify activity of expression protein. Methods The full - length human 14 - 3 - 3σ cDNA was obtained by RT - PCR and was then inserted into GV142 vector. After identification it was connected with pEGFP - N1 - SFN containing enhanced green fluorescent protein to recombine expression vector pEGFP - GV142 - SFN with 14 - 3 - 3σ. The pEGFP - GV142 - SFN plasmid was transfected to breast cancer MCF -7 to observe the expression of green fluorescent protein. Results Amplified ribosomal DNA restriction analysis and PCR and DNA sequencing showed that the target gene was inserted into the recombined plasmid. Fluorescence microscope showed that after 24 h transfection, expression of enhanced green fluorescent protein could be seen in MCF - 7, and the expression was the most stable at 48 h, and the protein quenched and cell morphology started to disappear at 72 h. Conclusion The construction of the eukaryotic expression vector pEGFP -GV142 -SFN is transfected into breast cancer MCF -7 ceils successfully to observe the expression of green fluorescent protein.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.117