查询词典 length of vector

Uniqueness of solution for generalized variational inequality related to strongly monotone Lipschitz mapping is shown. A sufficient condition is presented on the connectedness of solution set for the weak vector variational inequality on which the mapping is from a topological vector space X to L , where Y is also a topological vector space. The result is derived by discussing the properties of set-valued mapping induced by solution set of a scalar variational inequality related to the weak vector variational inequality.

利用拓扑向量空间到连续线性映射空间L的映射的弱向量变分不等式和与之相关的标量型变分不等式解集的关系，得到标量型变分不等式解集所表征的集值映射的特性和弱向量变分不等式解集的连通性条件。

This paper generalizes the conclusion of Perfect nonlinear S-boxes by Nyberg(1991), and introduces the conception of inverse regular generalized vector Bent function. It shows that for inverse regular generalized vector Bent function f with even variables, m is no more than half of?. It also shows that when the input dimension n is odd, the regular generalized vector Bent function and the inverse regular generalized vector Bent function do not exist. This may prevent the cryptology designer from seeking the inexistent function.

摘要该文完善并拓展了Nyberg(1991)的关于广义向量Bent函数性质的结论，相应于Nyberg给出的正则广义向量Bent函数，提出了&负则的广义向量Bent函数&的概念：得到有偶数个输入的负则的广义向量Bent函数输出维数也不大于输入维数的一半；证明了奇数个输入的正则和负则的广义向量Bent函数都不存在，这些结果的给出，可使密码设计者避免一味去寻找某类不存在的函数。

Reducing the complexity of vector quantization is still a main problem. This paper presents a new algorithm of minimum distortion predicting vector quantization based on intraband and interband correlation. Here the whole distortion of the vector is predicted by the part distortion of the lower frequency coefficient components of vector, resulting in a reduction of 76 percent of complexity.

降低矢量量化器的复杂度一直是人们研究的一个主要问题，本文提出一种新的基于带间相关性的最小失真预测矢量量化算法，通过矢量中前面部分低频系数分量失真的计算去预测整个矢量的失真，编码复杂度降低了76％，而解码图像信噪比下降不到1dB。

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。

The total proteins from TGIF transfectant and vector control cells were separated by 2D electrophorosis. 760±41 and 680±38 spots were detected in TGIF transfectant and vector control cells respectively. Locus repeat analysis of protein spots showed that the mean deviation in IEF direction in TGIF transfectant and vector control cells were 0.864±0.123 mm and 0.843±0.115 mm respectively whereas the mean deviation in SDS-PAGE direction in these two cells were 0.812±0.109 mm and 1. 125±0.123 mm respectively. So the well-resolved and reproducible 2DE patterns from TGIF transfectant and vector control cells were established.

通过双向凝胶电泳分别分离TGIF转染细胞和PcDNA3.1空白质粒转染细胞的总蛋白质，测得两组细胞的蛋白质斑点数分别为760±41和680±38个；位置重复性分析表明TGIF转染细胞在等电聚焦方向上的平均偏差为0.864±0.123mm，在垂直板SDS-PAGE电泳方向上的平均位置偏差为0.812±0.109mm；PcDNA3.1空白质粒转染细胞在IEF方向上的平均偏差为0.843±0.115mm，在垂直板SDS-PAGE电泳方向上的平均位置偏差为1.125±0.123mm。

The System inset remote sense vector data and GIS vector data in drainage area into client programs programmed, realizing the application of remote sense vector data and GIS vector data in water resources management of Xinjiang Ma-na-si River irrigation area, and realizing the integrated management of the texts and maps of the water resources survey data, and spatial analysis and map edit functions of GIS as well. The system, which breaks away the platform of MapInfo, can run independently.

该系统将流域中的遥感栅格数据与GIS矢量数据集成嵌入到所编制的客户程序中，实现遥感数据和GIS数据在新疆玛纳斯河流域水资源管理中的应用，和水资源调查数据图文一体化的管理，同时具备了GIS的空间分析和图形编辑等功能，该系统能脱离Mapinfo软件平台独立运行。

In this research we obtained the banana ACO gene with about 1.2kb length by cuffing from the cloning vector pUCm-ACO with restriction endonucleases Xba Ⅰ and Sac Ⅰ, and then directionally linked the gene to the plasmid vector pBⅠ-121 in the same endonucleases digestion sites, finally we got the construct of plant expression vector pBI-aACO.

用限制性内切酶Xba Ⅰ和sac Ⅰ从克隆载体pUCm-ACO上切下约1.2kb的香蕉ACO基因，将其定向连接在经相同酶切的质粒载体pBⅠ-121上，构建成植物表达载体pBⅠ-aACO。

Methods:The total RNA was extracted from mouse RAW264.7 cells stimulated by LPS.The sequence including the whole length of HMGB1 was amplified by RT-PCR and inserted into pMD-19T.The combinant vector was used as a template for PCR which was cloned into vector pMD-19T,then subcloned into expression vector pET-26b with pelB signal sequence and His-Taq sequence.After transforming E.coli BL21(DE3) and four hours induction by IPTG,HMGB1 expression confirmed by SDS-PAGE and the purification was performed by Ni2+-chelate affinity chromatograph.

脂多糖刺激后的RAW264.7细胞，提取总RNA，经RT-PCR扩增出含HMGB1的目的片段，克隆于pMD-19T载体，再亚克隆至含有pelB引导肽及His-标签肽的高效表达载体pET-26b，转化大肠杆菌BL21（DE3），经IPTG诱导后行SDS-PAGE鉴定目标蛋白表达，用镍鳌合琼脂糖凝胶亲和层析法分离纯化含His-标签肽的目的蛋白。

Methods:The total RNA was extracted from mouse RAW264.7 cells stimulated by LPS.The sequence including the whole length of HMGB1 was amplified by RT-PCR and inserted into pMD-19T.The combinant vector was used as a template for PCR which was cloned into vector pMD-19T,then subcloned into expression vector pET-26b with pelB signal sequence and His-Taq sequence.

脂多糖刺激后的RAW264.7细胞，提取总RNA，经RT-PCR扩增出含HMGB1的目的片段，克隆于pMD-19T载体，再亚克隆至含有pelB引导肽及His-标签肽的高效表达载体pET-26b，转化大肠杆菌BL21（DE3），经IPTG诱导后行SDS-PAGE鉴定目标蛋白表达，用镍鳌合琼脂糖凝胶亲和层析法分离纯化含His-标签肽的目的蛋白。

The thesis also gives the estimated upper bounds of error decision probability. When the compressor is confined to be a lattice vector quantizer, a explicit mathematic equation for the rate of the performance convergence to the optimum is derived. On the other hand, Distortion Ratio Aproachs to the design of testing system on the basis of vector quantization are put forward, and methods for building the variable length decision tree as well as the fixed length one presented.

在算法方面，提出了失真比矢量量化检验器的设计方法以及可变长和固定码长分类判决树的生成算法；为了解决以矢量量化器为核心的处理系统运算量大，不易实时实现的问题，论文中引入了熵减的概念，在此基础上提出一种快速最近邻搜索编码方法，理论分析及实验结果均证实了这种算法的有效性。

Article 144 The Government of the Hong Kong Special Administrative Region shall maintain the policy previously practised in Hong Kong in respect of subventions for non-governmental organizations in fields such as education, medicine and health, culture, art, recreation, sports, social welfare and social

第一百四十四条香港特别行政区政府保持原在香港实行的对教育、医疗卫生、文化、艺术、康乐、体育、社会福利、社会工作等方面的民间团体机构的资助政策。原在香港各资助机构任职的人员均可根据原有制度继续受聘。

Small wonder, then, that the Chinese spend more in the shop than any other group of foreign visitors do .

这样的小惊喜，使中国顾客比任何国家的人消费得更多。