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
   living cellular 的翻译结果: 查询用时:0.009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
 

living cellular
相关语句
  活细胞
     Application of Living Cellular Immunofluorescence Test in study of Immunoconjugate
     活细胞免疫荧光法在免疫偶合物研究中的应用
短句来源
     Results:KAC had an obvious inhibition activity on the human hepatoma cells,BEL- 7402,in vitro. With clonal formation and living cellular count the ED_(50) was 38.5mg/L and 54.0mg/L,respectively.
     结果:体外实验表明克癌胶囊能明显抑制人肝癌细胞 BEL-7402生长,ED_(50)在克隆形成法为38.5mg/L,活细胞计数法为54.0mg/L;
短句来源
     Methods:The experiments in vitro included clonal formation,living cellular count and N-acetyl-glucosamine trace-enzyme reactions,and experiments in vivo included tumor growth and living time of the mice beating tumor were detected.
     方法:分体外实验和体内实验,前者包括克隆形成法、活细胞计数法和 NAG 微量酶反应法; 后者主要观察荷瘤小鼠移植瘤的生长和小鼠的存活时间。
短句来源
     ②Activity of cartilage cells were detected with trypan blue dye exclusion test. Cellular vigor was caculated according to the formula below: Living cell rate (%)=total living cellular score/(total living cellular score+total dead cellular score) ×100%.
     ②锥虫蓝排斥试验检测软骨细胞活性,根据下式求细胞活力:活细胞率(%)=活细胞总数/(活细胞总数+死细胞总数)×100%。
短句来源
  相似匹配句对
     Living E.
     应用电镜细胞化学技术观察 E.
短句来源
     Application of Living Cellular Immunofluorescence Test in study of Immunoconjugate
     活细胞免疫荧光法在免疫偶合物研究中的应用
短句来源
     Methods:Micrography of Living Cells. Diagram of Cellular Growth.
     方法 :活细胞显微摄影、伊红染色细胞计数、绘制细胞生长曲线方法。
短句来源
     LIVING IN CITY
     住在都市里——建筑策划师与建筑师的对话
短句来源
     Cellular Chorioangioma of the Placenta
     胎盘富于细胞型血管瘤
短句来源
查询“living cellular”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。
  living cellular
Work in this area is discussed with reference to the use of isothermal microcalorimetry for the characterization of living cellular systems in the pharmaceutical industry.
      


Objective:To prove the effects of softening and resolving hard mass,a principle of TCM on hepatoma with Ke'ai capsule(KAC,an anti-tumor drug).Methods:The experiments in vitro included clonal formation,living cellular count and N-acetyl-glucosamine trace-enzyme reactions,and experiments in vivo included tumor growth and living time of the mice beating tumor were detected.Results:KAC had an obvious inhibition activity on the human hepatoma cells,BEL- 7402,in vitro.With clonal formation and living...

Objective:To prove the effects of softening and resolving hard mass,a principle of TCM on hepatoma with Ke'ai capsule(KAC,an anti-tumor drug).Methods:The experiments in vitro included clonal formation,living cellular count and N-acetyl-glucosamine trace-enzyme reactions,and experiments in vivo included tumor growth and living time of the mice beating tumor were detected.Results:KAC had an obvious inhibition activity on the human hepatoma cells,BEL- 7402,in vitro.With clonal formation and living cellular count the ED_(50) was 38.5mg/L and 54.0mg/L,respectively. While a cooperative action was observed in KAC and 5-FU(CDI<0.85,P<0.01).In vivo,with different dosage of KAC,1.8,3.6 and 7.2(g/kg per day),mean inhibition growth rate of tumor(HepA)in BALB/c mice was 16.6%(P >0.05),32.0%(P<0.05),and 49.8%(P<0.01),and the rate(T/C%)of delaying survival time of the mice bearing tumor(HepA)was 109%(P>0.05),135%(P<0.05)and 159%(P<0.01),respectively,and there were linear relations(P<0.01)between the dosages and the effects.The mean ratio of delaying survival time of the mice bearing ascites(HepA)with doses 3.6 and 7.2(g/kg,per day)was 110%(P>0.05)and 135%(P<0.05),respec- tively.Conclusion:KAC had the effects on hepatoma certainly and is worth to research further.

目的:通过实验方法揭示软坚散结方药——克癌胶囊的抗肝癌作用。方法:分体外实验和体内实验,前者包括克隆形成法、活细胞计数法和 NAG 微量酶反应法;后者主要观察荷瘤小鼠移植瘤的生长和小鼠的存活时间。结果:体外实验表明克癌胶囊能明显抑制人肝癌细胞 BEL-7402生长,ED_(50)在克隆形成法为38.5mg/L,活细胞计数法为54.0mg/L;与5-Fu 有显著的协同作用(P<0.05)。体内实验表明剂量为1.8、3.6、7.2g·kg~(-1)·d~(-1),对 BALB/C小鼠实体瘤(HepA)的抑瘤率(%)平均分别为16.6(P>0.05)、32.4(P<0.05)、49.6(P<0.01);生命延长率(%)平均分别为109(P>0.05)、135(P<0.05)、159(P<0.01),剂量与效应呈直线相关;剂量为3.6、7.2g·kg~(-)1·d~(-1),对 BALB/C 小鼠腹水癌(HepA)产生的抑制率(%)平均分别为14.2(P>0.05)、31.0(P<0.05);生命延长率(%)平均分别为110(P>0.05)、135(P<0.05)。结论:克癌胶囊有抗肝癌效果,与化疗药有协同增效作用。

The quantitative description of microbial community is one of the difficult tasks for microbial ecologist. Conventional cultivation techniques cannot be used to fully characterize most soil microorganisms in respect that most of species cannot be cultured. Using phospholipid fatty acids (PLFA) profiles to characterize microbial communities can overcome the limitation of traditional techniques, because it doesn't require the removal and the culture of the microbes. The membrane phospholipids exist in all living...

The quantitative description of microbial community is one of the difficult tasks for microbial ecologist. Conventional cultivation techniques cannot be used to fully characterize most soil microorganisms in respect that most of species cannot be cultured. Using phospholipid fatty acids (PLFA) profiles to characterize microbial communities can overcome the limitation of traditional techniques, because it doesn't require the removal and the culture of the microbes. The membrane phospholipids exist in all living cellular membrane. They are not found in storage products or in dead cells by reason of rapidly degradation after cells dying. PLFA don't vary much in a cell which they form a part, and keep reasonably constant amounts as cells occur in nature. The analysis of the ester-linked fatty acids of the phospholipids makes use of capillary gas chromatography and mass spectrometry. With such technique, the component of each PLFA and the shift in PLFA pattern can be quantitatively analyzed. PLFA profiles, consisted of quantitative determination of each PLFA component and the shift in PLFA patterns, can provide comprehensive information for detecting the microbial community. Several fatty acids are known to be “signatures” of subsets of microbial community. Therefore, the specific PLFA profiles can be used to characterize different groups of bacteria. Furthermore, a phospholipid pattern change in the related samples could be indications of a shift in microbial community. In fact, the PLFA technique has been used to illuminate the shifts in microbial community for adapting to the changed environmental conditions under wide range of soil types, management practices, climatic origins, etc. Although PLFA profile is unable to identify microorganisms at a species and strain level, it produces descriptions of the whole microbial community. It can be utilized to measure the viable microbial biomass and the community structure in environmental samples, such as sediments, soils, etc. Because of relative simplicity and good resolution, PLFA has become more and more popular. We introduced an analysis measurement of PLFA profiles and reviewed the published applications, including the assessment of microbial biomass, community structure, nutritional status and metabolic activity, in microbial ecology.

应用磷脂脂肪酸谱图分析技术对微生物群落进行定量分布 ,克服了传统的微生物培养方法和显微技术的局限性。介绍了磷脂脂肪酸谱图分析方法及其在微生物生态学领域中的应用 ,包括对微生物群落的生物量、群落结构、营养状况和新陈代谢活动等方面的研究。

AIM: To investigate the feasibility of preserving the activity of human anasl septum cartilage preservation at different cryopreserved temperature. METHODS: The experiment was conducted in the Postdoctoral Station for Pathophysiology, Basic Department of Fourth Military Medical University of Chinese PLA from March to September 2005. Fifteen blocks of adult anasl septum cartilage sized of 15 mm×10 mm were obtained by routine clinical septectomy and randomly divided into 3 groups with 5 blocks in each group, and...

AIM: To investigate the feasibility of preserving the activity of human anasl septum cartilage preservation at different cryopreserved temperature. METHODS: The experiment was conducted in the Postdoctoral Station for Pathophysiology, Basic Department of Fourth Military Medical University of Chinese PLA from March to September 2005. Fifteen blocks of adult anasl septum cartilage sized of 15 mm×10 mm were obtained by routine clinical septectomy and randomly divided into 3 groups with 5 blocks in each group, and then separately preserved under 4 ℃, -20 ℃ and -80 ℃. Viabilities of the cartilages were compared respectively at the 24th hour, and 7th, 14th, 20th, 30th day. ①Samples of cartilages were made into paraffin sections after fixed with 40 g/L formalin, cartilage cells and matrix were observed under light microscope after hematoxylin-eosin stainning and trypan blue staining. ②Activity of cartilage cells were detected with trypan blue dye exclusion test. Cellular vigor was caculated according to the formula below: Living cell rate (%)=total living cellular score/(total living cellular score+total dead cellular score) ×100%.RESULTS:①Paraffin sections of cartilage could be seen under the light microsope after hematoxylin-eosin staining and trypan blue staining: 24 hours after cryopreservation, cartilage lacunas of each group were mainly full of living cartilage cells and there were no marked changes in cartilage matrix. Activity of anasl septum cartilage was better. Cartilage cells were mainly degenerated after cryopreservation at -80 ℃ for 7days, -20 ℃ for 14 days and 30 days in each group, nucleus disappeared, reconstituents of stroma broke, intensity reduced. There were many degenerating cells in the middle part of cartilage after preserved at 4 ℃, while there were no obvious breaking phenomenons in acid mucopolysaccharide and collagen in cartilage matrix. ②After cryopreservation of cartilage at -80 ℃ for 24 hours, the activity of cartilage was 80%; 7 hours after the cryopreservation, there were hardly activity in the cartilage, cartilage cells and matrix maily degenerated. 24 hours after the cryopreservation of cartilage, the activity was 85%; there were mainly no activity in cartilage after 14 days. There was still better activity in cartilage after preserved at 4 ℃ for 1-20 days with the activity above 60% and there were no marked changes in cartilage cells and ingredients of matrix; Activity of cartilage decreased to 20% after 30-day-perservation. CONCLUSION: Cryopreservation at 4 ℃ and -20 ℃ within 2 weeks is a better way of preserving anasl septum cartilage, while that at 4 ℃ is much better, which may provide a better way of preserving active cartilage.

目的:探讨不同冷藏温度下保存成人鼻中隔软骨块活性的可行性。方法:实验于2005-03/09在解放军第四军医大学基础部病理与病理生理博士后流动站完成。取临床常规手术切除的成人鼻中隔软骨15块,切成大小约15mm×10mm,随机分成3组,每组5块。分别置入4℃,-20℃和-80℃冷冻保存,在保存24h,7d,14d,20d和30d时取材,进行软骨活性比较。①软骨样品于质量浓度为40g/L甲醛固定后制备石蜡切片,组织切片经苏木精-伊红染色和阿尔辛蓝染色后于光学显微镜下观察软骨细胞及软骨基质。②锥虫蓝排斥试验检测软骨细胞活性,根据下式求细胞活力:活细胞率(%)=活细胞总数/(活细胞总数+死细胞总数)×100%。结果:①软骨石蜡切片经苏木精-伊红染色和阿尔辛蓝染色后于光学显微镜下观察可见:冷冻保存24h时,各组软骨中大部分为活的软骨细胞充填软骨陷窝,软骨基质无明显变化,鼻中隔软骨活性程度较好。-80℃冷冻保存7d,-20℃保存14d及各组保存30d后,软骨细胞基本变性坏死,胞核消失,基质成份断裂、强度降低。4℃保存20d软骨中部有较多变性细胞,但软骨基质中酸性黏多糖及胶原成分无明显断裂现象。②-80℃冷冻保存软骨在保存...

目的:探讨不同冷藏温度下保存成人鼻中隔软骨块活性的可行性。方法:实验于2005-03/09在解放军第四军医大学基础部病理与病理生理博士后流动站完成。取临床常规手术切除的成人鼻中隔软骨15块,切成大小约15mm×10mm,随机分成3组,每组5块。分别置入4℃,-20℃和-80℃冷冻保存,在保存24h,7d,14d,20d和30d时取材,进行软骨活性比较。①软骨样品于质量浓度为40g/L甲醛固定后制备石蜡切片,组织切片经苏木精-伊红染色和阿尔辛蓝染色后于光学显微镜下观察软骨细胞及软骨基质。②锥虫蓝排斥试验检测软骨细胞活性,根据下式求细胞活力:活细胞率(%)=活细胞总数/(活细胞总数+死细胞总数)×100%。结果:①软骨石蜡切片经苏木精-伊红染色和阿尔辛蓝染色后于光学显微镜下观察可见:冷冻保存24h时,各组软骨中大部分为活的软骨细胞充填软骨陷窝,软骨基质无明显变化,鼻中隔软骨活性程度较好。-80℃冷冻保存7d,-20℃保存14d及各组保存30d后,软骨细胞基本变性坏死,胞核消失,基质成份断裂、强度降低。4℃保存20d软骨中部有较多变性细胞,但软骨基质中酸性黏多糖及胶原成分无明显断裂现象。②-80℃冷冻保存软骨在保存24h时,软骨细胞活性为80%;保存7d时软骨基本失去活性,软骨细胞及基质变性坏死。-20℃保存软骨在保存24h时,软骨细胞活性为85%;14d后软骨基本失去活性。4℃保存软骨在保存24h至20d时仍保持较好活性,软骨细胞活性保持在60%以上,软骨细胞及基质成分无明显变化;保存30d时软骨活性降为20%左右。结论:4℃和-20℃在2周内保存是较好的鼻中隔软骨保存方法,而4℃保存法更具优越性,有望为临床提供一种较好的活性软骨保存方法。

 
图标索引 相关查询

 


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