This research intended to construct a eukaryotic expression vector with a site-directed mutation of porcine MSTN propeptide gene.
本研究旨在构建具有猪 MSTN 前肽基因定点突变的真核表达载体。
The constructed expression vector expressed in E coli.
通过构建表达载体在大肠杆菌中得到了表达。
Objective to construct E. coli K99 pilus expression vector.
目的构建大肠杆菌K99菌毛表达载体。
Objetive to construct human IL 12 efficient expression vector.
目的构建人il -12的高效表达载体。
To clone gene of the TRAIL and construct its prokaryotic expression vector.
目的克隆人TRAIL基因，构建其原核表达载体。
Objective: to construct inhibin expression vector with high immunogenicity.
目的：构建高免疫原性的抑制素真核表达载体。
Objective To construct saccharomyces cerevisiae expression vector with GFP as report gene.
目的构建以绿色荧光蛋白（GFP）为报告基因的酿酒酵母表达载体。
Objective To produce recombinant HBcAg in insect cells by Baculovirus expression vector system.
目的利用杆状病毒表达载体系统制备重组乙型肝炎病毒核心蛋白。
Expression efficiency of the same expression vector is different in cells from different species.
同一载体在不同种属细胞内表达效率不同。
Objective: to obtain the procaryotic expression vector containing the antifreeze protein gene AFP.
目的构建可用于大肠杆菌表达系统的含抗冻蛋白基因afp的表达载体。
Objective to construct the eukaryotic expression vector of varicella-zoster virus (VZV) glycoprotein e.
目的构建水痘-带状疱疹病毒(VZV)糖蛋白e的真核表达载体。
Purpose: AQP4 M23 gene cloning and construction in the expression vector can provide us a research tool.
目的克隆大鼠水通道蛋白4（AQP4）M23基因并构建其载体为进一步研究提供理论基础和研究工具。
To construct the retroviral expression vector of Human P58.1 gene and study its expression in lymphocytes.
目的构建人P 58.1基因的逆转录病毒表达载体并探讨该基因在淋巴细胞中的表达。
Objective to clone human heat shock protein 70 (HSP70) gene for the construction of a prokaryotic expression vector.
目的克隆人热休克蛋白70 (HSP70)基因，构建其原核高效表达载体。
The NKG2D prokaryotic expression vector was successfully constructed. The recombinant NKG2D is expressed and purified.
完成了NKG2D的原核表达载体的构建，表达并纯化了重组NKG2D蛋白。
Results Saccharomyces cerevisiae expression vector with GFP as report gene was constructed and expressed successfully.
结果成功构建了以GFP为报告基因的酿酒酵母载体，并在酵母中得到表达。
Objective: To construct the recombinant expression vector of genes encoding light chain of antibody against Mumps Viruses.
目的：构建抗腮腺炎病毒抗体轻链基因重组表达载体。
Objective to construct a expression vector of MPT53 of mycobacterium tuberculosis and identify and purify the protein in the e.
目的构建结核杆菌分泌蛋白mpt53原核表达载体并进行表达和纯化。
Objective to construct an eukaryotic expression vector of compound multi-epitope gene of HCV and express the gene in COS7 cells.
目的建立丙型肝炎病毒(HCV)复合多表位基因的真核表达载体，并在COS7细胞中瞬时表达。
Results rat IL-10 eukaryotic expression vector had been constructed successfully, and had been transfected into rat chondrocyte.
目的构建大鼠il - 10真核表达载体并在大鼠软骨细胞中进行表达。
Human cancer suppressor gene, protein encoded therein, expression vector containing the same, and cell transformed by the vector.
人抑癌基因，其编码的蛋白，含有其的表达载体和由该载体转化的细胞。
The result indicated: in this system, the technique of eukaryotic expression vector providing poliovirus capsid protein was possible.
实验结果表明：该系统使用合适的真核表达载体提供脊灰病毒结构蛋白的技术路线是可行的。
Objective to construct recombinant human leptin mammalian cell expression vector, and to express recombinant human leptin in COS-7 cells.
目的构建重组人瘦素哺乳细胞表达载体并在COS 7细胞表达重组人瘦素。
Objective to construct eukaryotic expression vector of antisense MBD1 gene fragment and to provide a tool for studying MBD1 gene function.
目的构建反义MBD1基因片段真核表达载体，为研究MBD1基因功能提供工具。
Objective to construct the lentiviral expression vector of HLA-E gene and investigate its significance for further study on tumor immunity.
目的构建表达人类白细胞抗原- E (HLA - E)基因慢病毒载体，探讨慢病毒介导HLA - E基因在肿瘤免疫中的意义。
Conclusion: Recombinant expression vector PGL3-DF3-DTA could produce specific lethal effect on human breast cancer cell line of DF3 positive.
结论：重组表达载体PGL3 - DF 3 - DTA能对DF 3阳性的乳腺癌细胞产生特异性杀伤作用。
Results: A gene fragement encoding MCP-1 was cloned into the fusional expression vector PGEX-2T. DNA sequencing indicated that it was correct.
结果：将编码人单核细胞趋化蛋白—1（MCP—1）基因克隆至融合表达载体pGEX—2T中，DNA测序证实正确。
Objective: to construct eukaryotic expression vector of human death receptor (DR5) and transfect NS-1 cells to establish stable NS-1 cell line.
目的：构建人死亡受体5 (DR5)真核表达载体，转染NS - 1细胞，建立稳定转染的NS - 1细胞系。
The secretion expression vector of fusion gene in E. coli has constructed by fussing the proinsulin gene to the gene of staphylococcal protein a.
将胰岛素原基因融合到金色葡萄球菌蛋白a的基因上，构建成大肠杆菌中基因融合的外分泌表达载体。
The secretion expression vector of fusion gene in E. coli has constructed by fussing the proinsulin gene to the gene of staphylococcal protein a.
将胰岛素原基因融合到金色葡萄球菌蛋白a的基因上，构建成大肠杆菌中基因融合的外分泌表达载体。
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