1) plant expressional plasmid
植物表达质粒
1.
Objective: Construction of plant expressional plasmid pROP1 and pRPB1 of saliva-binding region(SBR) of surface protein antigen gene of Streptococcus mutans.
目的 :构建变形链球菌表面蛋白基因 (pac)唾液粘附区的植物表达质粒pROP1和pRPB1。
2) plant expression vector pBG1121
植物表达质粒pBG1121
3) plant recombinant expression plasmid
植物重组表达质粒
1.
The plant recombinant expression plasmid pBI GFP has been successfully constructed by cloning the green fluorescent protein gene which had been optimized by site directed mutagenesis into the plant expression vector pBI 121.
利用 DNA重组技术 ,将经定点突变改造的绿色荧光蛋白基因 ( gfp)克隆到植物表达载体p BI-1 2 1中 ,成功地构建了植物重组表达质粒 p BI-GFP。
4) 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。
5) 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：PUC18质粒DNA
CAS: 9007-49-2
中文名称: PUC18质粒脱氧核糖核酸；PUC18质粒DNA
英文名称: Deoxyribonucleic-acid；Calf thymus DNA；Desoxyribose nucleic acid；DNA；Nucleic acids, deoxyribo；deoxyribonucleic ac.；Nucleic acids,deoxyribo
中文名称: PUC18质粒脱氧核糖核酸；PUC18质粒DNA
英文名称: Deoxyribonucleic-acid；Calf thymus DNA；Desoxyribose nucleic acid；DNA；Nucleic acids, deoxyribo；deoxyribonucleic ac.；Nucleic acids,deoxyribo
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