查询词典 c.c.

The first design example is to generate program code for image processing controller to control picture file output and the second design example is a GPS satellite C/A code generator to generate the C/A code of GPS satellites. C/A code can be used to recognize GPS satellite number in GPS system.

最后我们使用两个例子来验证本工具，一个为影像处理控制器，其功能为控制图档输出功能，另一个为GPS卫星C/A码产生器，其功能在於能够产生太空中GPS卫星所使用的C/A码信号，C/A码在GPS系统中被用来识别GPS卫星编号。

Now this time taking C# users into account, every C++ code example in this article is accompanied by a C# code example.

现在这个时候考虑到C＃用户，每个C ++本文中的代码示例是伴随着C＃代码示例。

There had no significant difference between the groups in protein,fatty and water, the protein of group C was highest.From the result of nutrient constituent, the cholesterol content was determined in the Chinese herb additive groups.the relative content of group C was highest, the second and the third were B and D,they were 25.10%,22.04% and 21.40% respectively.

C、D、E组的系水力及熟肉率均优于A、B组；嫩度值对照组最低，说明肉质较嫩，C组最高为87.13，其次为B、D组，各个处理间的粗蛋白、粗脂肪及水分含量差异均不显著(P﹥0.05)。C组的粗蛋白含量高于其它组，粗脂肪含量略高于其它组。C组的氨基酸相对含量最高。

We show that Jordan multiplicative bijective maps on prime operator algebrasmust be additive. As its application, we show that every Jordan * multiplicative bijec-tive map on every factor C~* algebra is a C~* isomorphism or a conjugate C~* isomorphism,in the special case of B, it must be a *-isomorphism or a conjugate *-isomorphism.We also prove the additivity of Jordan multiplicative bijective maps on nest algebras.

证明了素算子代数上Jordan可乘双射的可加性，利用这一结论刻画了因子C~*代数上的Jordan*可乘双射，我们的结果表明这样的映射一定是C~*同构或共轭C~*同构；证明了套代数上的Jordan可乘双射的可加性。

Fill a clean, dry and accurately weighed pycnometer with the substance being examined (keep the temperature below 20°C or that specified under individual monograph), fix the thermometer (no air bubble is left in the pycnometer). Place the pycnometer in a water bath maintained at 20°C or the specified temperature, allow to stand in the water bath for several minutes, so as to raise the temperature of the content to 20°C or to the temperature specified in the monograph.

取洁净、干燥并精密称定重量的比重瓶，装满供试品（温度应低于20°C或各品种项下规定的温度）后，装上温度计，置20°C（或各品种项下规定的温度）的水浴中放置若干分钟，使内容物的温度达到20°C（或各品种项下规定的温度），用滤纸除去溢出侧管的液体立即盖上罩。

METHODS The HCV core gene coding region was inserted into the eukaryotic expressive plasmid pcDNA3, then the recombinant plasmid pcDNAHCV-C was constructed and expressed transiently with LipofectAMINE in the SP2/0 cells. After purification, these plasmid directly or encapsuled wit h Lipofect-AMINE were injected into BALB/c mice. HCV core antibody from immunized mice could be detected by ELISA. RESULTS The enzyme -cutting identification showed that HCV core gene fragment had been cloned into pcDNA3 eukaryote vectors.

人工构建包含HCV C基因片段的真核表达载体pcDNAHCV-C，在证实其可以在真核细胞中表达之后，将其用脂质转染剂包裹，形成LipofectAMINE-pcDNAHCV-C脂质混合物，将该混合物或单纯pcDNAHCV-C直接注射BALB/c小鼠股四头肌，以空载体pcDNA3做对照，ELISA法检测血清中抗体产生水平。

GA often uses C or Visual C++ to compile codes, so the program is not only long and cockamamie but also the efficiency is low and the velocity is slow. This paper uses software Matlab powerful calculating ability and many functions to compile programs, then encapsulate and link those programs to run without Matlab environment. At last use Visual C++ friendly alternate function to compile in-out interface.

针对遗传算法常用C或Visual C++编写源代码，程序庸长繁琐，效率不高，运行缓慢的特点，本文采用Matlab强大的数值计算能力和众多的库函数编写算法；然后封装和链接程序，使Matlab编写的算法能够完全脱离Matlab的编程环境；利用Visual C++良好的人机交互功能，用Visual C++编写算法的输入输出接口界面。

Results: 11 three dose of Kangzhitang has obviously reduced the concents of blood TC, TG, LDL-C, VLDL-C, apoB, LP , oxLDL, MDA and the ratio of TC/HDL-C of hyperlipidemia in rats: it has obviously raisen the concents of blood HDL-C, apoA-1 and the activity of SOD: it has obviously raisen the low density lipoprotein recepter mRNA , and been better than model group: the middle dose group is the most advantage.

结果：康脂汤高中低三个剂量均能显著降低实验性高脂血症大鼠血中的TC、TG、LDL-C、VLDL-C、apoB、LP、ox-LDL、MDA，显著升高血中HDL-C、apoAI水平及SOD活性，中剂量效果最好。治疗组大鼠低密度脂蛋白受体基因表达水平比模型组明显提高。

The minor core protein s C-encoding gene of Muscovy duck reovirus was cloned into theprokaryotic expression vector pET32a. The recombinant plasmid pET32a-s C was amplified andextracted after being transformed into E.coli DH5a competent cells. Restriction analysis withEcoRⅠand SacⅠand sequences analysis indicated that the recombinant plasmid was inserted withcorrect open reading frame. The fusion protein about 50 ku was produced after induction with 0.15mmol/L IPTG of E.coli competent cells transformed with pET32a-sC. The SDS-PAGE andWestern-bloting test indicated that the fusion protein reacted with the convalescents sera of duckinfected with Muscovy duck reovirus. The indirect ELISA method was developed by using thepurified fusion s C protein as coating antigen. The optimal concentration of s C was 5μg/ml, thedilution of serum sample was 1:40; The results showed that preparation of an ELISA by using sCas coating antigen in detecting 50 field duck sera in comparison with the AGIP were more sensitiveand specific than agar gel immuno-diffusion AGIP test. The results suggest that presence ofantibody against viral protein sC in duck may be a good indicator by the sC-ELISA for detectionof duck infection with reovirus.

同时，本研究将编码外壳蛋白σC的基因克隆于原核表达载体pET32a上，经过EcoRⅠ和SacⅠ双酶切鉴定和序列分析后，得到阳性重组质粒pET32a-σC；将阳性重组质粒pET32a-σC转化到大肠杆菌BL-21感受态细胞中进行诱导表达，经SDS-PAGE和Western-blbtting检测分析，融合表达的蛋白能够与番鸭呼肠孤病毒感染的康复鸭血清发生特异性反应；将融合表达的蛋白纯化后作为包被抗原，建立了检测鸭血清中呼肠孤病毒抗体的间接酶联免疫吸附试验检测方法，此方法中抗原的最佳包被浓度为5μg／ml、标准阳性血清的最适稀释倍数为1：40倍，用此方法对50份鸭血清样品进行检测，并与琼脂糖凝胶扩散试验检测抗体的法相比较，证明此ELISA方法具有良好的特异性和敏感性，本研究为今后鸭呼肠孤病毒诊断试剂盒的研制奠定了基础。

By cloning and sequencing those DNA fragments with polymorphisms we found 3 SNPs, they were as following: T→C in exon 3, G→C in introns 5,A→C in exon 6, in which A→C in exon 6 was non-synonymous substitution, it resulting in Thr→Arg.

对有多态的位点进行克隆测序，结果发现：外显子3中的一处碱基由T→C，是同义突变；内含子5中的一处碱基由G→C；外显子6中的一处碱基由A→C，是错义突变，导致苏氨酸变成精氨酸。

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。

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。