查询词典 dual cell
- 与 dual cell 相关的网络例句 [注:此内容来源于网络,仅供参考]
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Final cell structures obtained in dual depressurization are closely correlative to the solubility variation of CO2 under corresponding pressures.
两次降压得到的泡孔结构与该降压幅度下气体溶解度的变化密切相关
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DEMS combined with the dual thin layer flow through cell is a good tool for the quantitative study on the oxidation of small organic molecules.
微分电化学质谱仪与双薄层流动电解池结合是一个很好的定量研究小分子有机物氧化的有力工具。
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Therefore, DEMS with the dual thin layer flow through cell can be used to measure quantitatively the formation amount or rate of the gaseous or volatile species produced electrochemically on massive electrodes.
因此,由此电解池与DEMS结合可以用来定量测量块状电极上产生的气体或挥发性物质的量或生成速度。
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Bertalan ffy's General System Theory, by reasoning the evolutionaiy process of cell and indivi dual from analogy, man's niche in ecoystem is deduced: it is not only the linkage of food chain, but also the regular-controller in ecosystem.
这种划分对于自然生态系统或只有原始人的生态系统可能是非常正确的,但在今天,生物圈内几乎任何角落都有现代人的影响,而这种影响远非一个普通
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DEMS combined with the dual thin layer flow through cell was used to measure quantitatively the formation rate or amount of CO〓 and the consumption rate or amount of methanol during methanol oxidation.
本论文对一个新的双薄层流动电解池进行了表征。
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Objective Applies the dual immunity group dyeing,studies P53 and the cell keratin in pharyngeal cancer expression.
目的应用双重免疫组化染色法,研究P53与细胞角蛋白在鼻咽癌中的表达。
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During the test, it researches the different frequency cell reselection, direct RRC establishment, HSDPA redirection of common channel status terminal, different frequency handover based on coverage and quality, handover based on load. According to the test results, it gives suggestions on dual-carrier solution application scheme.
在测试过程中,对WCDMA双载波解决方案涉及的异频小区重选、HSDPA直接RRC建立、公共信道状态终端的HSDPA重定向、基于覆盖和质量的异频切换,以及基于负荷的切换等关键应用场景和算法进行了验证和研究,并根据测试结果提出了双载波解决方案的应用策略建议。
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It has the dual-prosperities of both cell membrane bioactivity and chromatographic separation. Coated with SD rat's epididymis lipocyte membrane, the silica was prepared for cell membrane stationary phase and a rat's adipose CMC model was ready.
其中,通过四氧嘧啶高血糖小鼠模型药效学实验证明,丹皮活性部位降低高血糖小鼠血糖具有显著性意义(P 。05),故确定为有效部位,进一步研究该部位的降血糖作用。
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Based on the laser longitudinal mode splitting theory, a novel scheme of dual-frequency laser with large frequency-difference is presented using electrically controlled birefringence of liquid crystal, and the transmitted resonant mode splitting by birefringent of Fabry-Perot etalon has been analyzed theoretically. A new element of liquid crystal Fabry-Perot etalon is designed and fabricated, which serves as aselector and splitter of both laser longitudinal modes and Fabry-Perot etalons transmitted resonant modes. Two different experimental systems of laser-diode end-pumped Nd:YAG laser have been set up using two different LDs, and the transmission of liquid-crystal cell have been measured. When the empty LCFP is inserted in the cavity of high-power LD pumped Nd:YAG laser, the oscillation of a single laser longitudinal mode have been observed, such a result shows that the designed and fabricated LCFP element is capable of selecting single axial mode. While an anti-reflected liquid crystal cell is inserted in the cavity of Nd:YAG laser end-pumped by the high-power LD, it is difficult to confirm weather the laser longitudinal modes have been spitted or not. The subject is summarized in this thesis and the improvement of the project has been presented.
论文以激光纵模的分裂理论为基础,提出了可望获得几十GHz甚至上百GHz的液晶电控双折射双频Nd:YAG激光器的总体方案,并对用双折射效应分裂F-P标准具透射谐振模进行了理论分析;设计并加工了一种集激光纵模选择、激光纵模分裂和F-P标准具谐振透射模分裂于一体的多功能元件——液晶电控双折射F-P标准具;建立了两种不同功率激光二极管端面泵浦的Nd:YAG激光实验系统,并对液晶盒的透射性质进行了测试;将未灌注液晶的空液晶F-P摘要标准具插入大功率LD泵浦Nd:、叭G激光谐振腔内,观察到了单纵模激光输出,说明所设计和加工的液晶F一P标准具具有纵模选择能力;将镀有增透膜的液晶盒插入大功率LD泵浦Nd八7AG激光谐振腔内,是否产生了激光纵模分裂现象还难以确定。
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The PCR products were examined by agarose gel electrophoresis. The target gene fragments were purified by gel extraction kit and ligated to cloning vector pMD18-T. The recombinant vectors were transformed into host strain E. coli K802 by lithium chloride method, screened and identified with PCR and restrictive enzymatic digestion. Their sequences were confirmed by DNA sequencing.(2) sTWEAK1 gene was subcloned into expression vector pProEx HTb and transformed into E. coli BL21. sTWEAK2 gene was subcloned into expression vector pMAL-C2x and transformed into E. coli TB1. The recombinant vectors were screened and identified with PCR and restrictive enzymatic digestion. The recombinant fusion proteins were induced to express with IPTG, detected by coomassie brilliant blue-stained SDS-polyacrylamide gel electrophoresis , and confirmed by Western blot analysis.(3) The sTWEAK1 fusion protein was purified with Ni-NTA Spin Kit.(4) The biological activity was assayed on transformed and tumor cells by microplate photometer after crystal violet or sulfur rodamine B staining.(5) The contents of IL-8 in the supernatant of 1990 cell cultures were determined by ELISA.(6) The morphological changes of the sensitive cells were observed by light and transmission electron microscopies.(7) The cell cycle and apoptotic rate were assayed by flow cytometry in 1990 and M85 cells.(8) The effect of fusion proteins on induction of NF-κB in 1990 and LOVO cells was detected with Dual-Luciferase Reporter Assay system.(9) The TWEAK gene was subcloned into Adeno-X Viral DNA with pShuttle vector and transfected into HEK293 cells by lipofectamine method.
(1)本研究用RT-PCR方法,从人组织细胞总RNA中扩增可溶性TWEAK胞外区(sTWEAK1和sTWEAK2)的cDNA序列及全长编码序列,用琼脂糖凝胶电泳分析PCR产物,胶回收目的基因片段,连接到pMD18-T克隆载体中,转化大肠杆菌K802,PCR和酶切筛选阳性克隆,全自动DNA测序验证序列;(2)sTWEAK1和sTWEAK2分别亚克隆到pProEx HTb和pMAL-C2x表达载体中,分别转化大肠杆菌BL21和TB1,PCR筛选和酶切鉴定,阳性克隆用IPTG诱导表达,表达产物用SDS-PAGE分析和Western blot验证融合蛋白;(3)用NTA-Ni Spin试剂盒初步分离纯化sTWEAK1融合蛋白;(4)用体外培养的肿瘤细胞和正常对表达产物进行活性检测,贴壁细胞用结晶紫染色法,悬浮细胞用磺酰罗丹明B染色法,酶标仪检测OD值;(5)敏感细胞用ELISA法检测细胞培养上清中IL-8的含量;(6)用光镜和电镜观察敏感细胞死亡和细胞凋亡情况;(7)用流式细胞仪分析表达产物对敏感细胞凋亡率和细胞周期的影响;(8)用双荧光素酶报告基因检测法,测定表达产物对敏感细胞NF-κB的影响;(9)用pShuttle穿梭质粒将TWEAK重组到腺病毒载体上,用脂质体转染法转染HEK293细胞,PCR鉴定重组质粒。
- 推荐网络例句
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This one mode pays close attention to network credence foundation of the businessman very much.
这一模式非常关注商人的网络信用基础。
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Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.
扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。
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There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.
双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。