1) binary expression plasmid
表达双元质粒
5) expression vector
表达质粒
1.
PurposeThe expression vector pTYB102 was constructed and active expression of nattokinase gene in E.
目的构建大肠杆菌表达质粒pTYB10 2 ,实现纳豆激酶基因 (nattokinasegene)在大肠杆菌中高活性表达。
2.
Recombinant expression vector was constructed and sequenced after enzyme digestion.
方法 :采用RT -PCR技术 ,从正常人外周血单个核细胞中扩增编码CD1 5 8b的cDNA ,经酶切后将其克隆于pMBP -c表达质粒上 ,酶切和测序鉴定。
3.
The full-length cDNA fragment encoding human C1-INH was obtained by gene recombination techniques and a stable expression plasmid was constructed by inserting the human C1-INH cDNA into an efficient dicistronic expression vector pED.
利用基因工程手段获取编码人补体1抑制物（C1-inhibitor，C1-INH）的基因片段，将其插入双顺反子表达载体pED中，构建成功可在CHO细胞中有效表达人C1-INH的表达质粒。
6) Expression plasmid
表达质粒
1.
Construction and identification of siRNA expression plasmid aimed at UL49 gene of Marek′s disease virus RB1B strain;
马立克氏病病毒超强毒UL49基因siRNA表达质粒的构建与鉴定
2.
Sequence analysis and eukaryotic expression plasmid constructionof gE gene of pseudorabies virus strain MinA;
伪狂犬病病毒Min-A株gE基因序列分析及其真核表达质粒的构建
3.
Here, a expression plasmid that suitable for Agrobacterium-mediated transformation pUNDV was constructed, which carried fussion protein gene of Newcastle disease virus(NDV-F) under the control of ubiquitin(Ubi) promoter, the selectable marker hygromycin phosphotranferase gene(HPT) and the reporter glucuronidase gene(GUS).
以编码新城疫病毒融合蛋白(NDV-F)的基因为外源基因,以玉米泛素蛋白(Ubi)启动子为启动子熏以潮霉素磷酸转移酶穴HPT雪基因作为选择标记基因熏β-半乳糖苷酸酶(GUS)基因作为报告基因构建了适宜于农杆菌介导转化水稻的表达质粒pUNDV,并通过农杆菌介导转化水稻,获得了多株转基因植株。
补充资料：元质
1.即元素。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条