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Recombinant plasmid pEGFP-C1-GnRH/TRS showed good genetic stability in HeLa cells.

质粒pEGFP-G1-GnRH/TRS在HeLa细胞中有较好的遗传稳定性。

The CCND2 expression cell proliferation, cell cycle and cell apopotosis of the transfected LP-1 cells were studied by RT-PCR, trypanosome staining, flow cytometry and annexin V assay.

设计、合成CCND2短发夹RNA双链DNA模板,构建表达质粒pGenesil-2/CCND2,转染LP-1细胞,以RT—PCR检测对CCND2表达的抑制作用,以锥虫蓝染色计数和MTI检测细胞增殖,以Annexin V检测细胞凋亡,流式细胞术检测细胞周期。

In this experiment, His 5 gene was inserted into Ura 3 gene and constructed a new plasmid pLRH33, which contained a complete His 5 gene and partial Ura 3 gene at the ends of His 5 gene.

实验将His 5基因插入到一个Ura 3基因的中间,构建了一个新的质粒pLRH33,从而打断了Ura 3 基因使之不能表达。

Methods: The coding region of superoxide dismutase was amplified using PCR method from the E.co1i genome. The PCR product was cloned into PUC19-T vector and sequenced. In addition, the cloned coding region of Mn-SOD was inserted into the expression vector PET-28a to form the recombinant plasmid PET-28a-Mn-SOD and was then transformed into E.coli BL21 for expression.

用PCR方法从大肠杆菌2号基因组中扩增Mn-SOD基因编码区,克隆到pUCm-T Vector,测定核苷酸序列;再将基因编码区克隆到原核表达载体PET-28a,构建含Mn-SOD基因的重组表达质粒,转化到大肠杆菌BL21中进行IPTG诱导表达。

Fourth, we constructed pBES-CFA/I vectorial vaccine and test the expression of CFA/I by SDS-PAGE.

第四、构建了pBEGFP-CFA/I 载体疫苗表达质粒,并进行了SDS-PAGE检测。

Reverse Transcription-Polymerase Chain Reaction was used to clone the whole-length gene of BMP-2 and construct AdV vector.

应用反转录-聚合酶链反应法克隆出骨形态发生蛋白质类2全长基因,构建重组腺病毒载体,DNA-磷酸钙共沉法将辅助质粒PJM17转染293细胞,同源重组构建出重组腺病毒。

Abjective to express the Hepatitis A virus genome cDNA attenuated salmonella Typhimurium and to find the immunity to hepatitis A virus after administrated that salmonella Typhimurium with hepatitis A virus gemome to the mousehepatitis A virus coding region cDNA were inserted expressive plasmid PBV221 and then were transform into E coli DH5α.

使甲型肝炎病毒基因组cDNA能够在减毒伤寒杆菌中表达,从而通过口服此种减毒伤寒杆菌达到对甲肝免疫的作用。将甲肝病毒编码区cDNA插入高效表达质粒PBV221,转化大肠杆菌DH5α,筛选并鉴定阳性克隆。

Oral administration of DNA nanoparticles synthesized by complexing pCMVβ DNA with chitosan,which modified with gelatin,Sodium Alginate,PEG and acetylize respectively,resulted in transduced gene expression in the intestinal epithelium.

分别使用明胶、海藻酸钠、PEG及乙酰化修饰包裹含LacZ的质粒pCMVβ的壳聚糖纳米颗粒,通过口服发送后经X-gal染色检测目的基因在小鼠体内的表达。

It was identified that the nif gene for aerogenic P. agglomerans strain waslocated on plasmid while for anaerogenic strains were located on chromosomes usingKlebsiella pneumoniae nifHDK as probe.

用nifHDK为探针进行Southern杂交证明固氮成团泛菌产气型的菌株固氮基因定位在质粒上,而不产气型菌株固氮基因定位在染色体上。

A new method was adopted to study the amidation of HNP expressed as fused protein.

以此为基础构建了环化表达质粒,并对表达条件进行了探索。

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