2) chimeras
嵌合表达
1.
Study of the chimeras of Pseudomonas aeruginosa exotoxin A and HSV-2-gD and its immunogenicity;
绿脓杆菌外毒素A与Ⅱ型单纯疱疹病毒糖蛋白嵌合表达质粒的构建及其免疫原性的研究
3) fusion-expression plasmid
融合表达质粒
1.
Porcine granulocyte-macrophage colony-stimulating factor (GM-CSF ) gene amplified from porcine (Sus scrofa )expression plasmid pGM-CSF by PCR was subcloned into somatostatin eukaryotic expression plasmid pcS/2SS to construct fusion-expression plasmid (pGM-CSF/SS) harboring porcine GM-CSF and somatostatin (SS ).
从猪(Sus scrofa)真核表达质粒pGM-CSF PCR扩增猪粒细胞-巨噬细胞集落刺激因子(GM-CSF)基因的编码序列,亚克隆到生长抑素真核表达质粒pcS/2SS中,构建GM-CSF与生长抑素(SS)基因的融合表达质粒pGM-CSF/SS,酶切鉴定和DNA测序证明重组的融合表达质粒pGM-CSF/SS构建正确。
4) chimeric plasmid
嵌合质粒
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：嵌合质粒
分子式：
CAS号：
性质：用DNA克隆技术构建的、含有一种以上生物体DNA序列的重组质粒。也可泛指由不同来源的DNA构成的任何杂种质粒。
CAS号：
性质：用DNA克隆技术构建的、含有一种以上生物体DNA序列的重组质粒。也可泛指由不同来源的DNA构成的任何杂种质粒。
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