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Expression and Beat Frequency in Rat Myocardial Cells

质粒介导shRNA对心肌细胞kir2.1蛋白表达和搏动频率的影响

Methods Cadmium-specific promoter PcadA was obtained by PCR from pPcadA and was ligated to E.coli-B.subtilis shuttle vector pNGFP with gfp being reporter gene ,after which the recombinant plasmid was transformed into 1A751 strain to form the bio-engineered bacteria.

采用聚合酶链式反应从质粒pPcadA上扩增得到重金属镉离子特异性启动子PcadA,以绿色荧光蛋白基因为报告基因,以大肠杆菌-枯草杆菌穿梭载体pNGFP构建了绿色荧光蛋白镉离子诱导表达载体。

METHODS To analyze its biotype,antibioticgram,serotype,plasmidgram and their relationship combining the clinical test examination.

方法结合检验工作,先后用生物分型、抗菌谱分型、血清分型和质粒图谱分型,再交互分析其关系。

Objective: To Construct and identify the bivalent recombinant baculovirus transfer plasmid of HPV type 16 and type 11 gene.

目的:构建人乳头瘤病毒16型与11型L1基因双价重组杆状病毒转移质粒并对其进行鉴定。

The tetraploid embryos were obtained from diploid blastomere electrofusion which preformed at 2-cell stage.

通过电穿孔的方法将增强型绿色荧光蛋白表达质粒转入ESCs,用G418筛选获得EGFP-ESCs。

Objective To construct a prokaryotic expression vector encoding first 193 amino acids of BPI N terminal.

目的:建立杀菌/渗透增强蛋白 N 端193个氨基酸的重组表达质粒

Objective To construct a prokaryotic expression vector encoding first 193 amino acids of BPI Nterminal.

目的:建立杀菌/渗透增强蛋白 N端193个氨基酸的重组表达质粒

Results A 579 bp fragment was amplified by RTPCR. BPI cDNA was inserted into pET28a.

结果:从HL60细胞中扩增得到579 bp的BPI 193基因片段,构建了TBPI 193亚克隆和PETBPI 193重组表达质粒

In this report, we constructed a new suicide plasmid to construct Brucella mutant.

本研究构建了一个可用于布鲁氏菌突变株构建的自杀质粒

Using this plasmid, we constructed replacement mutant of Brucella omp25 gene.

利用该质粒,我们构建了布鲁氏菌外膜蛋白Omp25基因的突变株。

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