CHO细胞,CHO cells英语短句,例句大全

CHO细胞,CHO cells
1)CHO cellsCHO细胞
1.Construction of decorin expression vector and its expression in CHO cells;核心蛋白聚糖真核表达载体的构建及其在CHO细胞中的表达
2.Effect of wild-type and mutant DNA polymerase β expression on CHO cells growth;不同类型的DNA聚合酶β基因对CHO细胞的影响
3.Expression of murine bcl-X_L gene in CHO cells;鼠bcl-X_L基因在CHO细胞中的表达

英文短句/例句

1.Improvement of Anti-HBsAg Antibody Production in CHO Cell;抗HBsAg抗体在CHO细胞中表达量提高研究
2.Construction of CHO Cells Stably Expressing CCR5;CCR5稳定表达的CHO细胞的构建
3.Construction of CHO Cell Line Stably Expressing Mouse Lamada-Interferon稳定表达鼠IFN-λ的CHO细胞系建立
4.Optimization of Manufacturing Process of Recombinant CHO Cell Hepatitis B Vaccine重组CHO细胞乙肝疫苗生产工艺的优化
5.Expression of Full-length MBL Gene of Han Chinese in CHO Cells汉族人MBL全长基因在CHO细胞中的表达
6.Purification and Activity of Recombinant Human IL-12(CHO Cells)重组人白细胞介素-12(CHO细胞)的纯化及其活性
7.Stable Expression of the Recombinant Human Membrane Form Klotho Protein in CHO Cells;重组人膜型Klotho蛋白在CHO细胞中的稳定表达
8.Study on High-level Expression of Recombinant Hepatitis B Surface Antigen in CHO Cell;重组CHO细胞高效表达乙肝表面抗原的研究
9.Stable Expression of the Human Secreted Form Klotho Protein in CHO Cells;人分泌型KL蛋白在CHO细胞中的稳定表达
10.Manufacture of Collagen Carriers and Its Application in CHO Cell Culture;胶原蛋白载体制备及在CHO细胞培养中的应用
11.The stable expression of the fusion gene pEGFP-rhPLD2 in CHO cell linepEGFP-rhPLD_2融合基因在CHO细胞株中的稳定表达
12.Construction of CHO cells MAR sequence and construction of Retrovirus vectorCHO细胞MAR片段的克隆及其逆转录载体的构建
13.Establishment of CHO cell line stably expressing cannabinoid receptor 2稳定表达大麻受体2的CHO细胞株的构建
14.Study on Exogenous PDI Gene Transferred into CHO Cells to Assist in the Secretion of HBsAg外源PDI基因导入CHO细胞及其对HBsAg分泌的影响
15.Clone and Expression of Human Cytomegalovirus Phosphoprotein 65 Gene in Chinese Hamster Ovary Cell;人巨细胞病毒PP65基因的克隆及在CHO细胞中的表达
16.Pilot Production Procedure of Adsorbed Acellular DTP-Recombinant Hepatitis B(CHO Cells)Combined Vaccine吸附无细胞百白破-重组乙型肝炎(CHO细胞)联合疫苗的中试工艺
17.Expression of Recombinant sPDGFRα-Fc in CHO and Its Anti-proliferation Analysis在CHO细胞中表达重组sPDGFRα-Fc及其抑制细胞增殖的研究
18.The Chinese Hamster Ovary Cells Apoptosis Induced by X-ray Irradiation;电离辐射致中国仓鼠卵巢（CHO）细胞凋亡

相关短句/例句

CHO cellCHO细胞
1.Construction of eukaryotic expression vector of HBsAg and its expression in CHO cell;HBsAg真核表达载体的构建及其在CHO细胞中的表达
2.Establishment and identification of the CHO cell lines which express attenuated mutants of Shiga-like toxin Ⅰ;稳定表达突变减毒志贺样毒素Ⅰ的CHO细胞株的建立与鉴定
3.Determination of hOP-1 full-length gene expression in CHO cells and biological activity of rhOP-1;hOP-1全长基因在CHO细胞的表达及活性检测
3)CHOCHO细胞
1.Expression of CSFV E0 gene in CHO cells;猪瘟病毒E0基因在CHO细胞中的表达
2.A STUDY ON CYTOKINESIS BLOCK MICRONULEUS (CBMN) TECHNOLOGY IN CHO CELL;CHO细胞胞质分裂阻断微核技术的研究
3.Methods The inhibitory effects of genistein on the proliferation of human gatric cancer cell line SGC-7901,human lung cancer line YTMLC-90,Chinese hamster ovary cell line CHO and peripheral blood lymphocyte from healthy person were studied.方法　观察染料木黄酮对肺癌YTMLC -90、胃低分化腺癌SGC - 790 1、中国仓鼠卵巢CHO细胞株体外增殖和正常人外周血淋巴细胞活性和功能状态的影响。
4)CHO-K1 cellsCHO-K1细胞
1.Expression of porcine Toll-like receptor TLR2 gene in the CHO-K1 cells;猪TOLL样受体2基因在CHO-K1细胞中的表达
2.And finally,pcDNA3/hLIF was introduced into COS-7 cells and CHO-K1 cells by using the method of lipofectin transfection,and transient expression and stable expression of hLIF protein was obtained respectively.利用脂质体介导将这一表达载体导入COS-7细胞和CHO-K1细胞,分别获得了hLIF的瞬时表达和稳定表达,为进一步进行hLIF生物学功能研究和hLIF在哺乳动物细胞中的高表达研究奠定了基础。
5)CHO/dhfr~-cellCHO/dhfr-细胞
1.AIM: To obtain CHO/dhfr~- cells line with integrated FRT sequence in the chromosome transcription active site and to express human-mouse chimeric antibody directed against Chikungunya Virus by using the cell line.以此载体转染CHO/dhfr-细胞,用1g/L的G418筛选抗性克隆。
6)CHO-K1 cellCHO-K1细胞
1.Methods CHO-K1 cells were transfected by pSNAV-signal-syn BPI_(m600)-Fcγ1_(700) expression vector,positive cell clones which high-expressed BPI_(m23)-Fcγ1 were selected with Dot blot and cultured in PF-CHO medium to express functional BPI_(m23)-Fcγ1 recombinant protein.方法用pSNAV-signal-syn BPIm600-Fcγ1700转染CHO-K1细胞,通过Dot blot筛选获得高表达BPIm23-Fcγ1目的蛋白的阳性细胞克隆,经PF-CHO培养基扩大培养,获得分泌表达的BPIm23-Fcγ1重组抗菌蛋白。
2.pIRES-N was transfected into CHO-K1 cells with coprecipitation, and positive cells were screened with hygromycine selection.然后通过磷酸钙共沉淀法转染CHO-K1细胞,通过潮霉素筛选得到阳性克隆,间接免疫荧光实验(IFA)鉴定N基因在CHO细胞中的表达,并用RT-PCR方法从转录水平证实N基因在CHO-K1细胞中的表达,最终建立了CHO/CDV-N细胞株,为犬瘟热病毒的血清学检测和基因疫苗的研制奠定了基础。
3.Objective:To optimize the condition of gene transient transfection in CHO-K1 cell.目的:以CHO-K1细胞为宿主基因瞬时转染条件的优化。