助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   dna technology 的翻译结果: 查询用时:0.2秒
图标索引 在分类学科中查询
所有学科
畜牧与动物医学
公安
生物学
更多类别查询

图标索引 历史查询
 

dna technology
相关语句
  dna技术
     By using the recombinant DNA technology,four expression plasmids,pGEX-BoPrP(23-242),pGEX-BoPrP(100-242),pGEX-CaPrP(25-241) and pGEX-CaPrP(93-241),of yak and camel recombinant prion proteins were constructed,After transforming E.
     应用重组DNA技术构建了牦牛和双峰驼重组朊蛋白的4个表达载体,即pGEX-BoPrP(23~242)、pGEX-BoPrP(100~242)、pGEX-CaPrP(25~241)和pGEX-CaPrP(93~241),经转化E.
短句来源
     Methods: The anti-transferrin receptor (TfR) ScFv-GAL4 fusion protein expression vector ScFv-GAL4pET28a and the eukaryotic expression plasmid pEBAF/tk-GAL4rec were constructed by recombinant DNA technology.
     方法 通过重组DNA技术分别构建anti-TfR ScFv-GAL4融合蛋白表达载体ScFv-GAL4-pET28a及含AFP启动子、GAL4特异性识别序列(GAL4rec)的HSV-tk真核表达载体pEBAF/tk-GAL4rec。
短句来源
     Application of Windows DNA Technology in Video Monitor System
     Windows DNA技术在视频监控系统中的应用
短句来源
     Study on Plate Rolling Control System Based on DNA Technology
     基于DNA技术的中厚板轧制控制系统的研究
短句来源
     In this paper, we mainly research in ASP, Component Technology, XML, DHTML and WINDOWS DNA Technology.
     文中重点研究了ASP技术,组件技术,XML技术,DHTML技术和WINDOWS DNA技术
短句来源
更多       
  “dna technology”译为未确定词的双语例句
     Methods:The anti-TfR ScFv-GAL4 fusion protein expression vector ScFv-GAL4-pET28a and the eukaryocyte expression plasmid pEBAF/tk-GAL4rec were constructed by recombinant DNA technology.
     方法:通过重组技术分别构建anti-TfR ScFv-GAL4融合蛋白表达载体ScFv-GAL4-pET28a及合AFP启动子、GAL4特异性识别序列(GAL4rec)的HSV-tk真核表达载体pEBAF/tk-GAL4rec。
短句来源
     Results 423 bp fragment including conservative region of hMTH1 gene was obtained by RT-PCR. After cloned by pGEM-T vector and certified by DNA sequencing,pEGFP-C1-T vector was successfully constructed by means of recombinant DNA technology.
     结果 经RT PCR获得 42 3bp产物 ,T载体克隆后 ,经DNA测序 ,确定该片段为hMTH1基因cDNA ,进而构建反义RNA真核表达载体pEGFP C1 T ,测序后确证。
短句来源
     Prophylactic vaccines based on the use of virus-like particles (VLPs) obtained from auto-assembly of L1 or L1 and L2 proteins produced by recombinant DNA technology are under phase I/II clinical trials for HPV6/11 associated with condylomas.
     通过DNA重组技术,基于HPV6/11型L1或L1和L2蛋白自我组装成病毒样颗粒的研究已经进入了I/II期临床实验。
短句来源
     Application of DNA technology to gynecological tumors
     DNA芯片技术在妇科肿瘤中的应用
短句来源
     Methods:An artificial egf gene was constructed with recombinant DNA technology and inserted into pQE-40 to get a expression plasmid pQE-EGF,in which egf was fused with 6×His tag. Plasmid pQE-EGF was transformed into E.
     方法:用DNA重组技术构建EGF基因并插入表达载体pQE-40,与载体上的6×H is标签融合,获得的表达质粒pQE-EGF转化E.
短句来源
更多       
  相似匹配句对
     DNA Chip Technology
     DNA芯片技术
短句来源
     Progress of DNA chip technology
     DNA芯片技术的研究进展
短句来源
     TECHNOLOGY
     技术
短句来源
     Technology;
     技术;
短句来源
     coli DNA.
     其效能优于大肠杆菌DNA
短句来源
查询“dna technology”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  dna technology
Glazko, Russian-English-Ukrainian Explanatory Dictionary of Applied Genetics, DNA Technology, and Bioinfo
      
We have used a biologically relevant rat model of meningitis in conjunction with classical microbial genetics and recombinant DNA technology to investigate the molecular basis ofHaemophilus influenzae pathogenicity.
      
The application of recombinant DNA technology to allergen research has provided the sequence information and genetic material to produce new types of allergy vaccines.
      
The major capsid protein of papillomaviruses, L1, when expressed by recombinant DNA technology, has the intrinsic ability to assemble into virus-like particles (VLPs).
      
Recently, advances in monoclonal antibodies and recombinant DNA technology have resulted in the development of new drugs to arrest disease progres-sion and restore physiologic immune responses without major side effects.
      
更多          


As a consequence of the spreading of recombinant DNA technology,a lot of genes have been isolated from the complex genome DNA.Making restriction map is usually of first importance in further analysis of the cloned gene fragments.The terminal labeling method for restriction map analysis would often have trouble when the fragmeat size is large.The terminal fragment hybridization method reported here could overcome this difficulty,and the restriction map can be elucidated easily by using labeled terminal...

As a consequence of the spreading of recombinant DNA technology,a lot of genes have been isolated from the complex genome DNA.Making restriction map is usually of first importance in further analysis of the cloned gene fragments.The terminal labeling method for restriction map analysis would often have trouble when the fragmeat size is large.The terminal fragment hybridization method reported here could overcome this difficulty,and the restriction map can be elucidated easily by using labeled terminal fragment as probe and hybridization with a series of partial digested fragments.This method is simple,universal and new.

由于基因工程技术的出现,很多基因可以由复杂的基因组中分离纯化。进一步分析基因结构的工作,首先便是酶切图谱的分析。本文报道的末端片段杂交法,是一种方便、通用的新方法。

HBcAg was synthesized in E. coli using recombinant DNA technology. The antigen in crude bacterial lysate was a satisfactory diagnostic reagent when used in ELISA for detecting antibodies to HBcAg in serum samples.It correlated well with results obtained by using HBcAg extracted from human liver and those from corresponding Abbott kit. When compared with routine laboratory diagnosis test using only RPHA for HBsAg, it gave 8.9% and 16.5% higher positive cases (serum dilution 1:100)in screening serum samples...

HBcAg was synthesized in E. coli using recombinant DNA technology. The antigen in crude bacterial lysate was a satisfactory diagnostic reagent when used in ELISA for detecting antibodies to HBcAg in serum samples.It correlated well with results obtained by using HBcAg extracted from human liver and those from corresponding Abbott kit. When compared with routine laboratory diagnosis test using only RPHA for HBsAg, it gave 8.9% and 16.5% higher positive cases (serum dilution 1:100)in screening serum samples from 2040 blood donors and 158 clinically suspected hepatitis patients respectively. The crude antigen can be purified by one step affinity chromatography separation.

以HBcAg的基因重组到能表达的大肠杆菌MM206株,制备了大肠菌HBcAg的粗提物。用酶联免疫吸附检测时只与抗-HBc发生特异的免疫学反应,与人肝HBcAg进行对比性平行检测78份血清标本,结果完全一致,与Abbott药盒检测抗-HBc的结果相比较,总符合率为97.3%。用于筛选献血员,阳性检出率较只测HBsAg高8.9%,对临床肝炎病人的阳性检出率也较只测HBsAg高16.5%。粗制HBcAg经亲和层析可一步纯化到电泳一条主带上。对该抗原应用情况和纯化问题进行了讨论。

Two murine hybridoma cell lines secreting monoclonal antibodies against piginsulin were obtained from one fusion by using pig insulin as immunogen.One of thetwo,hybridoma 4B9,secreted monoclonal antibodies of IgG_1 type.The titers determinedby ELISA were in the range of 10~(-2)-10~(-3) in culture supernatants and 10~(-6)-10~(-7) inascitic fluid of BALB/C mice.The affinity constant(Ka)of the McAb to pig insulinwas 5.86x10~9L/M.The McAb cross-reacted with human insulin produced by recom-binant DNA technology....

Two murine hybridoma cell lines secreting monoclonal antibodies against piginsulin were obtained from one fusion by using pig insulin as immunogen.One of thetwo,hybridoma 4B9,secreted monoclonal antibodies of IgG_1 type.The titers determinedby ELISA were in the range of 10~(-2)-10~(-3) in culture supernatants and 10~(-6)-10~(-7) inascitic fluid of BALB/C mice.The affinity constant(Ka)of the McAb to pig insulinwas 5.86x10~9L/M.The McAb cross-reacted with human insulin produced by recom-binant DNA technology.

用猪胰岛素免疫的 BALB/C 小鼠脾细胞,与小鼠骨髓瘤细胞 NS-1融合,获得两株分泌抗猪胰岛素单克隆抗体的杂交瘤细胞,命名为4B9和3B2。其中,以4B9细胞的抗体分泌能力最强。其培液抗体的 ELISA 效价为10~(-2)~10~(-3);注入同系小鼠腹腔诱生的腹水抗体效价达10~(-6)~10~(-7)。其分泌抗体属 IgG_1亚类;对猪胰岛素的亲和常数(Ka)为5.86×10~9L/mole;与用 DNA 重组技术制备的人胰岛素,呈交叉反应。

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关dna technology的内容
在知识搜索中查有关dna technology的内容
在数字搜索中查有关dna technology的内容
在概念知识元中查有关dna technology的内容
在学术趋势中查有关dna technology的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社