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作 者:刘晓军 郝琴琴 李鹏飞[2] LIU Xiao-jun;HAO Qin-qin;LI Peng-fei(Comprehensive Convenience Service Center of Jinshanpu Township,Fanshi County,Xinzhou City,Shanxi Province,Fanshi,Shanxi 034300;College of Life Science,Shanxi Agricultural University,Taigu,Shanxi 030801)
机构地区:[1]山西省忻州市繁峙县金山铺乡综合便民服务中心,山西繁峙034300 [2]山西农业大学生命科学学院,山西太谷030801
出 处:《中国牛业科学》2023年第1期41-45,共5页China Cattle Science
基 金:山西省应用基础研究计划面上项目(20210302123380);山西农业大学校地合作项目(2021HX23,2022HX010);山西省现代农业产业技术体系建设专项。
摘 要:[目的]构建以及鉴定牛lncRNA H19过表达重组载体,为进一步探究lncRNA H19与miRNA 491和牛CART基因的互作关系奠定试验基础。[方法]NCBI获取牛lncRNA H19序列,经聚合酶链式反应(PCR)扩增,双酶切后载入pcDNA3.1-EGFP载体得到重组质粒。将pcDNA3.1-EGFP-H19、miRNA 491和CART 3种质粒共转染至HEK293T细胞,在细胞内反复扩增过表达之后,利用荧光定量技术检测pcDNA3.1-EGFP-H19的表达量。[结果]结果显示pcDNA3.1-EGFP-H19载体序列正确;293T细胞绿色荧光达50%,且强度适中,说明转染效果良好;lncRNA H19在293T细胞中显著表达。[结论]pcDNA3.1-EGFP-H19载体构建成功,试验将为后续探究lncRNA H19与miRNA 491和CART基因之间的互作关系创造试验条件。[Objective]To construct and identify lncRNA H19 overexpression recombinant vector,to lay the experimental foundation for further exploring the interaction between lncRNA H19,CART gene and miRNA 491.[Method]LncRNA H19 sequence was obtained by NCBI,amplified by polymerase chain reaction(PCR),double digested and loaded into pcDNA3.1-EGFP vector to obtain recombinant plasmids.The three plasmids were transfected into HEK293T cells.After repeated intracellular amplification and overexpression,purification and titer detection were performed.[Result]Finally,the expression of lncRNA was detected by fluorescence quantification,and the sequence of pcDNA3.1-EGFP-H19 vector was correct.The green fluorescence of 293T cells reached 50%,and the intensity was moderate,indicating that the transfection operation was correct.lncRNA H19 was significantly expressed in 293T cells.[Conclusion]pcDNA3.1-EGFP-H19 vector was successfully constructed.This study will create experimental conditions for further exploring the interaction between lncRNA H19,miRNA 491 and CART gene.
关 键 词:pcDNA3.1-EGFP-H19 荧光定量技术 CART 细胞转染
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