表达质粒,Expression plasmid
1)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。
英文短句/例句
1.Construction of multidrug resistance gene(MDR1) short hairpin RNA expression plasmidMDR1 shRNA表达质粒的构建
2.Construction and expression of the eukaryotic expression plasmid of Human pEGFP/H2B人类pEGFP/H2B真核表达质粒的构建及表达
3.The Expression of NgR mRNA in the Optic Nerve and the Construction of NgR Specific siRNA Encoding Vector;视神经NgR mRNA的表达及其siRNA表达质粒载体的构建
4.Construction and Expression of pGEX-4T-2-TK Procaryon Recombinant PlasmidpGEX-4T-2-TK原核表达质粒的构建及其表达
5.Construction of miRNA-451 expression plasmid and its inhibitory effect on the expression of iNOS genemiRNA-451表达质粒的构建及其对iNOS基因表达的抑制
6.Vector construction and eukaryotic expression of the human GITR_(aa1-165)-IgG1FchGITR_(aa1-165)-IgG1Fc真核表达质粒的构建及其表达
7.Construction and Sequence Analyzing of the Recombinant Plasmid Affecting Gene HPV6bL1 Translation by RNA Interfering;HPV6bL1短发夹shRNA表达质粒的构建及鉴定
8.The Construction and Identification of pcDNA3.1-Osx;pcDNA3.1-Osx真核表达质粒的构建和鉴定
9.The Construction of Rat Interleukin-6 Gene Eukaryotic Expression Vector;大鼠IL-6基因真核表达质粒的构建
10.Construction and identification of eukaryotic expression vector pEGFP-N1/BMP-2pEGFP-N1/BMP-2真核表达质粒的构建与鉴定
11.Construction of eukaryotic expression vector DINH and C3d3 fusion geneDINH与C3d3融合基因真核表达质粒的构建
12.Construction and determination of a recombinant eukaryotic plasmid pcDNA3.1(+)-h/mCD44v6真核表达质粒pcDNA3.1(+)-h/mCD44v6的构建和鉴定
13.Construction and determination of a recombinant eukaryotic plasmid pcDNA3.1(+)-rmCGβ真核表达质粒pcDNA3.1(+)-rmCGβ的构建和鉴定
14.Construction and Screening of RNAi Expression Vector for Murine Chk1 Gene小鼠Chk1基因RNAi表达质粒的构建与筛选
15.Construction of HPV16E6 Gene Plasmid Expressing in Prokaryotic SystemHPV16 E6基因原核表达质粒的构建
16.Construction and Indentification of the Recombinant Expression Plasmid pcDNA3.0-SV40TpcDNA3.0-SV40T重组表达质粒的构建及鉴定
17.Exploration of Optimal Expression Conditions in Lactobacillus Casei with pPG Vector;乳酸杆菌pPG质粒表达系统理想表达条件的探索
18.Construction and Expression of hTERT Recombinant Plasmids;hTERT重组质粒的构建及其表达
相关短句/例句
expression vector表达质粒
1.PurposeTheexpression 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.Recombinantexpression 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 dicistronicexpression 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。
3)plasmid expression质粒表达
4)Coexpression plasmid共表达质粒
1.AIM: To construct an eukaryotic coexpression plasmid pSLC-IRES-IL-2, and to express it in COS-7 cells.目的:构建共表达质粒pSLC-IRES-IL-2,并在COS-7细胞中表达。
5)Co-expression plasmid共表达质粒
1.Effects of co-expression plasmid of human tPA and VEGF165 on the proliferation of vascular cells and fibrinolysis activity;tPA和VEGF165基因共表达质粒对人血管细胞增殖的影响和纤溶作用
6)double expression plasmid双表达质粒
延伸阅读
PUC18质粒DNACAS: 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
