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The results of its 1D test demonstrate that the MARED code is suitable for simulating implosions on different devices and with a wide range of load parameters. Combination of the wire-array Z-pinch experiment simulation and analysis shows that under the same load conditions, the X-ray radiation power produced by the tungsten wire-array implosion is much greater than the power generated by the aluminum wire array. With the same load current, the greater load mass gains the lower X-ray power.

结合丝阵Z箍缩实验的数值模拟和分析表明：相同负载质量条件下，钨丝阵内爆产生的X光辐射功率远大于铝丝阵产生的X光功率；相同负载电流条件下，负载质量越大，计算得到X光功率越低；X光功率随着负载电流增加而增加。

This research take late-maturing variety adzuki bean Jihong-4 as the experiment material, After the photoperiod inducement at different leaf ages treatment, the result showed that the activity of NR under LF treatment is higher than CK treatment on the whole, and is lower than SD treatment; The content of the dissociation amino acid under these three treatments show a descend trend along with the leaf ages accretion, but the inducement increasing the content of dissociation amino acid, different leaf ages leaves show some difference, and alternating rise with SD treatment; Inducement can reduce the content of soluble sugar, and continuous inducement shows a accumulation effect; 2LF is the most sensitivity stage for soluble protein under photoperiodic inducement, From this stage, each leaf indumenta can reducing the content soluble protein, but continuous inducement reducing rising it.

本研究通过光周期诱导的方法，对中晚熟品种冀红4号红小豆进行不同叶龄进行处理，结果表明：所有叶龄处理下硝酸还原酶活性基本高于自然光处理而低于连续短日照处理下的；随着叶龄增大，各处理游离氨基酸总量均呈下降趋势，但光周期诱导可提高游离氨基酸含量，不同叶龄表现有所差异，与连续诱导交替上升；诱导可降低可溶性糖的含量，并连续诱导出现累积效应；2LF是光周期诱对可溶性蛋变化最敏感的时期，这个时期起单个叶龄诱导可降低可溶性蛋白含量，但连续诱导却可提高；LF处理下的类胡萝素总体含量高于另两个处理，而LF处理下的叶绿素含量在仅3叶龄前高于CK处理下的，随后出现下降趋势。

This experiment utilizing cell biology together with molecular biology technique begins with the above-mentioned three researching heatpoints to research the effect that SLT interposes MCs biology action and to strive to clarify the part of cell molecular biology mechanism of SLT'therapeutic action.

本研究利用细胞生物学与分子生物学技术，从上述三个研究热点入手，多层面地研究SLT 干预MCs 生物学行为的效应，力图阐明SLT 治疗作用的部分细胞分子生物学机制。

Blood samples were collected from mice in each group and the hematological parameters were detected at the end of the experiment.RBC,HGB,HCT,MCV,MCH and MCHC of the mice in the model group were significantly lower than those in the control group.Compared with the model group,RBC,HGB,HCT,MCV,MCH and MCHC were increased significantly,but WBC,Lym and Mid were reduced significantly in the experimental Group 3 administered with high dose of polysaccharides solution.

结果显示，模型组小鼠的血液指标红细胞数、血红蛋白浓度、血细胞比容、平均红细胞体积、平均红细胞血红蛋白含量、平均红细胞血色素浓度显著低于对照组的相应指标；与模型组相比，给予高剂量姬松茸水溶性粗多糖的试验组3的血液指标RBC、HGB、HCT、MCV、MCH、MCHC均显著提高，而白细胞数、小型白细胞数和中型白细胞数则显著下降。

Experiment results indicate that the magnetic fluid flux has a direct relation with the magnetic field under the effect of traveling wave magnetic field. The bigger the magnetic field is, the more the flux is, when the structure of the magnetic fluid travellig pump and the saturation magnetization of magnetic fluid are constant. The volumes of the magnetic fluid from the travelling wave pump increase from 1.9 ml to 3.1 ml, when the magnetic field intensity increases from 25 900 A/m to 40 000 A/m. In addition, the change rate of the magnetic fluid decreases with the increase of the magnetic field due to the effect of magnetic field on magnetic fluid viscosity. The bigger the saturation magnetization of the magnetic fluid is, the more the flux is.

结果表明，行波磁场作用下的磁性流体流量与磁场的强度有直接关系：在磁性流体行波泵结构和磁性流体饱和磁化强度相同的条件下，磁场强度越强，其流量越大；当磁场强度从25900A/m增加到40000A/m时，单位时间内从行波泵内流出的磁性流体的体积由1.9 ml增加到3.1 ml；随着磁场强度的不断增加，磁性流体流量的变化率由于磁场对其粘度的影响而减小；而磁性流体的饱和磁化强度越大，其流量也越大。

Methods: The experiment was conducted by inducing the cataract of rats with galactose and raising the rats with maize yellow pigment.

用半乳糖诱发大鼠白内障，喂饲玉米黄色素进行了实验研究。

The metal pipes with different material and different thickness were acted as the metal-coated in experiment, and the gap between the fiber and the metal-pipe was filled with epoxy evenly.

实验中采用不同材料、不同厚度的金属套管充当金属镀层，光纤与金属套管间的缝隙用环氧树脂均匀填充。

Was extracted with 95% ethanol at first,and then the ethanolic extract was separated with petroleum ether, ethyl acetate, n-Butyl alcohol and methanol in turn to get four fractions from small to large in polarity. The MTT experiment was made for active screening.

方法青天葵部位提取物的制备主要采用溶剂法，青天葵全草先用95%的乙醇提取，得到的提取物进一步用石油醚、醋酸乙酯、正丁醇、甲醇依次提取，得到极性由小到大的4个提取部位。

Then modelings with multi-body dynamics software ADAMS, so that the analyzing results should be more accurate with the experiment checked.

然后利用多体动力学软件ADANMS进行建模，并利用相关实验验证了理论分析的结果，使结论更为准确和可靠。

The monoclonal antibody was produced by the method of inoculating BALB/c mice intraperitoneally with the hybridoma cells, and purified with protein A-Sepharose 4B affinity chromatography.3 Establishing of ELISA protocol to detect hBLySTwo kind of different ELISA protocols were tried to study the experiment condition of detecting hBLyS level. Streptavidin was used to indirect coating in protocal 1, but biotin-avidin system was used to enlarge the final reaction signal in protocal 2. The optimal reaction condition was chosen by the experiments. The sensitivity of protocal 1 was poor, but the linear relation of protocal 2 standard curve was excellent when the concentration of hBLyS was between 3.2~400 ng/mL. So a protocal was established which sensitivity can reach to nanogram.

建立检测hBLyS蛋白含量的ELISA方法选用2种ELISA方案对hBLyS蛋白含量的测定方法进行研究，方案一用链霉亲和素做间接包被，方案二用生物素-亲和素系统做终反应放大；优化选择2种检测方法的反应条件；方法一的敏感度较低：方法二在hBLyS蛋白浓度为3.2～400 ng/mL范围内，标准曲线的线性关系良好；从而建立了一种可检测hBLyS蛋白浓度为ng级水平的ELISA方法。

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。