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
   subcellular region 的翻译结果: 查询用时:0.119秒
图标索引 在分类学科中查询
所有学科
更多类别查询

图标索引 历史查询
 

subcellular region
相关语句
  亚细胞区域
     Methods The translocation of PKC in subcellular region was observed in L9981 before and after nm23-H1 gene transfection and Calphostin C treatment by Laser scanning confocal microscope (LSCM) method. Results PKC-α and PKC-βⅡ were found to locate in different subcellular site in L9981 before and after nm23-H1 gene transfection.
     方法 应用激光扫描共聚焦显微镜观察nm 2 3 H1基因转染前后和CalphostinC处理转基因细胞株L9981 nm2 3 H1前后PKC在不同的亚细胞区域的定位情况。
短句来源
     If probes cannot differentiate and load special subcellular region, fluorescent imaging cannot attain satisfied calcium information of the subcellular region.
     目前,细胞内游离Ca~(2+)的研究主要是用荧光探针标记,然后通过荧光显微成像分析来实现的,在此探针的性能至关重要,探针若不能区分标记特定亚细胞区域,荧光显微镜也就根本无法得到有关区域的Ca~(2+)信息。
短句来源
  “subcellular region”译为未确定词的双语例句
     Objective To explore the influences of nm23-H1 gene transfection and protein kinase C (PKC) inhibitor Calphostin C on PKC signal transduction pathway in human high-metastasis large cell lung cancer cell line L9981, and to evaluate the effects of nm23-H1 gene on translocation and activation in subcellular region.
     目的 探讨nm2 3 H1转染和蛋白激酶C(PKC)特异抑制剂CalphostinC对人高转移大细胞肺癌细胞株L9981细胞PKC信号转导通路的作用 ,以及nm2 3 H1基因对PKC激活转位的影响。
短句来源
  相似匹配句对
     Culture Region
     文化区
短句来源
     shock region.
     三个区域对应了时域的激波形成。
短句来源
     Progress on subcellular proteomics
     亚细胞蛋白质组研究进展
短句来源
     Progress on Subcellular Proteomics
     快速发展的亚细胞蛋白质组学
短句来源
查询“subcellular region”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。
  subcellular region
Little or no external AChE activity was detected in non-endplate muscle regions and the internal enzyme was confined to a restricted subcellular region close to the point of innervation.
      
Consequently, the observed differences in the insulin-like activity between the complexes would reflect the potency of the two compounds in the +IV and +V oxidation states in the subcellular region.
      
For years this was assumed to be the main role for Ca2+ in this specialized subcellular region.
      
The molecular mechanism that underlies the localization of Kv4.2 to this subcellular region is unknown.
      
The crucial issue is to delineate each subcellular region through a process known as segmentation.
      


Sixteen Scenedesmus species or strains have been employed to investigate the maximum capacity of nickel (Ni) accumulation in 10 mg/L Ni solution. The results showed that the capacity of accumulating Ni from aqueous solution in 16 Scenedesmus species or strains showed the diversity. S. quadricauda freshwater algae culture collection of the Institute of Hydrobiology (FACHB) 44 and S. quadricauda FACHB 506 performed much more capacity of Ni accumulation than other species such as Scenedesmus ...

Sixteen Scenedesmus species or strains have been employed to investigate the maximum capacity of nickel (Ni) accumulation in 10 mg/L Ni solution. The results showed that the capacity of accumulating Ni from aqueous solution in 16 Scenedesmus species or strains showed the diversity. S. quadricauda freshwater algae culture collection of the Institute of Hydrobiology (FACHB) 44 and S. quadricauda FACHB 506 performed much more capacity of Ni accumulation than other species such as Scenedesmus sp. FACHB 416 and Scenedesmus sp. FACHB 489. Sequestration of Ni ions from aqueous solution was very efficient (26.7 mg Ni/g dry weight, in the 100 mg/L Ni solution) in S. quadricauda FACHB 44. The kinetics of Ni binding indicated that Ni bioaccumulation, in algal cell of S. quadricauda FACHB 44, possessed a rapid biosorption (5 min) and an slow bioaccumulation (2-3 h). More than 70% of Ni binding in algal cell were accumulated by biosorption and the remaining 20%-30% were bioaccumulated by energy_consumed transportation. It is much more higher ratio of energy_consumed transportation in S. quadricauda FACHB 44 than in other algae. Both the transmission electron microscope (TEM) and the energy_dispersive X_ray (EDX) microanalyses also revealed the different mechanisms of bioaccumulation in the various subcellular regions: a very fast adsorption in the cell wall; and a time_dependent absorption in protoplasm, specially in starch and chromatin.

对不同Scenedesmus品种的藻细胞从含镍水溶液 (10mg/L)中累积金属镍的能力进行了分析 ,结果表明 :藻细胞对镍的生物累积量表现出明显的品种差异性。ScenedesmusquadricaudaFACHB 4 4和ScenedesmusquadricaudaFACHB 5 0 6表现出很强的累积能力 (累积量达到 5~ 6mgNi /g干重 ) ,而Scenedesmussp .FACHB 4 16和Scenedesmussp .FACHB 4 89在相同条件对金属镍累积量要少得多 (1~ 1.5mgNi /g干重 )。这种差异可能与不同品种藻细胞间的形态结构和生理特性是相关的。对S .quadricaudaFACHB 4 4重金属抗性和累积能力进一步的分析表明 ,S .quadricaudaFACHB 4 4用于含镍重金属废水处理是非常有效的 ,在高浓度 (10 0mg/L)的镍溶液中 ,藻细胞的最大累积量能达到 (2 6 .7mgNi/g干重 )。对该藻细胞镍累积动力学分析发现 :藻细胞对镍的生物累积包括一个快速的被动吸附过程 (5min ,结合 70 %的镍 )和一个缓慢的耗能累积过程 (2~...

对不同Scenedesmus品种的藻细胞从含镍水溶液 (10mg/L)中累积金属镍的能力进行了分析 ,结果表明 :藻细胞对镍的生物累积量表现出明显的品种差异性。ScenedesmusquadricaudaFACHB 4 4和ScenedesmusquadricaudaFACHB 5 0 6表现出很强的累积能力 (累积量达到 5~ 6mgNi /g干重 ) ,而Scenedesmussp .FACHB 4 16和Scenedesmussp .FACHB 4 89在相同条件对金属镍累积量要少得多 (1~ 1.5mgNi /g干重 )。这种差异可能与不同品种藻细胞间的形态结构和生理特性是相关的。对S .quadricaudaFACHB 4 4重金属抗性和累积能力进一步的分析表明 ,S .quadricaudaFACHB 4 4用于含镍重金属废水处理是非常有效的 ,在高浓度 (10 0mg/L)的镍溶液中 ,藻细胞的最大累积量能达到 (2 6 .7mgNi/g干重 )。对该藻细胞镍累积动力学分析发现 :藻细胞对镍的生物累积包括一个快速的被动吸附过程 (5min ,结合 70 %的镍 )和一个缓慢的耗能累积过程 (2~ 3h时间内的累积量占总量的 2 0 %~ 30 % )。与其他藻类相比 ,S .quadricaudaFACHB 4 4对水溶液中镍的耗能累积量明显高于其他藻类。透射电子显微镜(TEM)和X射线能谱 (EDX)分析结果均表明 ,藻细胞耗能累积的镍主要集中在原生质体中 ,尤以淀粉粒和染色质中为多。

Objective To explore the influences of nm23-H1 gene transfection and protein kinase C (PKC) inhibitor Calphostin C on PKC signal transduction pathway in human high-metastasis large cell lung cancer cell line L9981, and to evaluate the effects of nm23-H1 gene on translocation and activation in subcellular region. Methods The translocation of PKC in subcellular region was observed in L9981 before and after nm23-H1 gene transfection and Calphostin C treatment by Laser scanning confocal microscope...

Objective To explore the influences of nm23-H1 gene transfection and protein kinase C (PKC) inhibitor Calphostin C on PKC signal transduction pathway in human high-metastasis large cell lung cancer cell line L9981, and to evaluate the effects of nm23-H1 gene on translocation and activation in subcellular region. Methods The translocation of PKC in subcellular region was observed in L9981 before and after nm23-H1 gene transfection and Calphostin C treatment by Laser scanning confocal microscope (LSCM) method. Results PKC-α and PKC-βⅡ were found to locate in different subcellular site in L9981 before and after nm23-H1 gene transfection. PKC-α and PKC-βⅡ mainly located in nucleus and perinucleus in L9981 and L9981-pLXSN cell lines, which were in active status. PKC-α and PKC-βⅡ mainly located in soluble cytosolic fraction in L9981-nm23-H1 cell line and were inactive status. PKC-α and PKC-βⅡ mainly located in cytosolic fraction and were in inactive status in all the three cell lines after treatment with Calphostin C. Conclusion The results suggest that nm23-H1 gene might make PKC to translocate from nucleus and perinucleus to soluble cytosolic fraction in L9981 cell line. PKC inhibitor, Calphostin C, can also make PKC to translocate from nucleus and perinucleus to soluble cytosolic fraction in L9981, L9981-pLXSN cell lines. Both transfection of nm23-H1 gene and treatment with Calphostin C can suppress the PKC signal transduction in L9981 cell line.

目的 探讨nm2 3 H1转染和蛋白激酶C(PKC)特异抑制剂CalphostinC对人高转移大细胞肺癌细胞株L9981细胞PKC信号转导通路的作用 ,以及nm2 3 H1基因对PKC激活转位的影响。方法 应用激光扫描共聚焦显微镜观察nm 2 3 H1基因转染前后和CalphostinC处理转基因细胞株L9981 nm2 3 H1前后PKC在不同的亚细胞区域的定位情况。结果  ( 1)原代细胞株L9981和空载体细胞株L9981 pLXSN中PKC α、PKC βⅡ主要位于胞核及核周 ,处于激活状态 ;转染nm 2 3 H1基因后的人肺癌细胞株L9981 nm2 3 H1中PKC α、PKC βⅡ主要位于胞浆 ,处于未激活状态。 ( 2 )CalphostinC作用后所有细胞中的PKC均主要位于胞浆中 ,处于未激活状态。结论  ( 1)nm2 3 H1基因可使L9981细胞株中PKC从胞核向胞浆转位 ,从而抑制PKC信号转导。 ( 2 )CalphostinC可使L9981、L9981 pLXSN细胞株中PKC从胞核向胞浆转位 ,从而抑制PKC信号转导。

 
图标索引 相关查询

 


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