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Results The penumatization rate of total or inferior part of middle turbinate correlated positively to the inflammation of anterior ethmoid and maxillary sinuses. Compared with patients with normal frontal sinuses, the vertical diameters of agger nasi cells of patients with frontal sinusitis were larger(11.70±5.50 mm and 8.54±3.67 mm respectivevy, p＜0.01).Compared with patients with normal maxillary sinuses, the Haller's cells of patients with maxillary sinusitis were larger (77.8% and 33.3%,P＜0.05)and the amount of inflammatory Haller's cells of the latter was more abundant than that of the former(91.6±17.8 mm2 and 41.6±12.6 mm2, respectively, P＜0.05). The deviation of uncinate process was one of the factors of maxillary sinusitis .The sizes of ethmoid bullae increased with the soft tissue thickening in anterior ethmoid sinus, the large ethmoid bulla may cause anterior ehmoid sinusitis.

结果 全中甲或中甲下部气化的发生率随前筛、上颌窦内软组织影增厚而升高；有额窦炎组病人的鼻丘气房最大纵向垂径明显大于无额窦炎组(分别为11.7±5.5 mm和8.5±3.7 mm，P＜0.01)；Haller气房在上颌窦炎组和非上颌窦炎组的发生率无显著差异，但前组发生炎症的Haller气房明显多于后组(分别为77.8%和33.3%，P＜0.05)，且前组Haller气房的冠状位截面积明显大于后组(分别为91.6±17.8 mm2和41.6±12.6 mm2，P＜0.05)；钩突角度随上颌窦内软组织增厚而减小；筛泡冠状位截面积随前筛窦内软组织增厚而增大(P＜0.01)。

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 results of cold-flow model test indicate:(1) the pressure drop rises with increasing air quantity and solids quantity respectively, however, much more air quantity and solids quantity minish in the same height position;(2) the pressure drop rises with increasing solids quantity;(3) the average granule concentration minishes with increasing air quantity, and rises with increasing the granule quantity in the same level position;(4) the inhomogeneity of distribution granule concentration minishes with increasing air quantity, and rises with increasing the granule quantity in the same level position.

结果表明：(1)在同一高度截面上，循环流化床反应器炉膛内压降随风量的增加而增加，但是风量过于增大反而使压降在同一截面上减小；(2)压降随初始物料量的增加而增加；(3)在同一水平截面上，颗粒浓度随风量的增大而逐渐减小，随物料量的增大而增大；(4)颗粒浓度分布的不均匀性随风量的增大逐渐减小，随物料量的增加不断增大。

The automatic dryer are expected, or auto-transport function, can automatically feed-share level even after drying into the box; box multi-mobile network with stainless steel materials can automatically flip, hot Bottom-up flow through the network with its network with the top layer of material, heat and mass transfer uniform, full, high-productivity, product quality, good-looking color, with flow-through dryer equipped with cooling and vibration levels expected to lose Device, a low-temperature materials is conducive to packing in a timely manner; chain network dryer with the door activities, to facilitate the clean-up day

该烤箱设有自动均料、自动升运功能，可把料物自动摊平后均匀的送入烘干箱内；箱内采用多层移动式不锈钢网带可使料物自动翻转，热气流自下而上穿过网带及其网带上面的物料层，热质交换均匀、充分，生产效率高，产品质量好，色泽好看，烘干烤箱设有冷却层和震动输料装置，出料温度低，有利于及时包装；烘干烤箱设有活动门，便于每天清理

objective to establish immunological methods specific for detecting antigens in different groups of monoclonal antibodies.methods indirect immnofluorescence assay was applied to identify specificity of the two groups of monoclonal antibodies prepared with crude antigen and recombinant antigen of aspergillus fumigatus,respectively.two different double monoclonal antibody sandwich elisa assays established with the two groups of antibodies were performed to detect antigents in the cell culture supermatants of 19 common species of aspergillus,penicillium marneffei,and 5 species of candidas.results the results of indirect immnofluorescence assay indicated that the monoclonal antibodies prepared with crude antigen of aspergillus fumigatus were specific for antigens in both clinical isolates and environmental isolates of aspergillus, whereas the other group of monoclonal antibodies was proved to be specific for aspergillus fumigatus of both clinical and environmental isolates.the elisa assay established with the crude antigen-specfic monoclonal antibodies could detect both of the clinical and environmental isolates of aspergllius, while the other assay could only detect aspergillus fumigatus of both clinical and environmental isolates.and no cross reaction with the cell culture of penialllium marneffei and candidas was observed with the two methods.conclusion the elisa assays can detect both of the clinical and environmental isolates of aspergillus,and differentiate aspergillus fumigatus from other species of aspergillus.

目的 用2组曲霉单克隆抗体建立特异性识别不同种类曲霉抗原的检测方法。方法采用天然烟曲霉抗原免疫，获得广谱针对曲霉抗原的单克隆抗体；采用重组烟曲霉抗原获得特异性针对烟曲霉抗原的单克隆抗体，用间接免疫荧光鉴定，并分别建立2种双抗体夹心elisa法，对19种常见的环境和临床分离曲霉株、马尔尼菲氏青霉菌及念珠菌培养液进行检测。结果间接免疫荧光显示，用天然烟曲霉抗原免疫获得的单克隆抗体(mabs-1)可广谱识别多种曲霉分离株，而重组烟曲霉抗原获得的单克降抗体(mabs-2)仅能特异性结合临床和环境分离的烟曲霉抗原。用mabs-1建立的双抗体夹心elisa法可检测19种常见曲霉株培养液；用特异性针对烟曲霉抗原单克降抗体(mabs-2)建立的双抗体夹心elisa法可特异性检测临床和环境分离株烟曲霉培养液；与其他曲霉株无交叉反应；2种双抗体夹心elisa法与马尔尼菲氏青霉菌及念珠菌培养液均无交叉反应。

XL26 backfilling the main characteristics of compactors are used before and after the frame hinged connections, four-wheel independent hydraulic drive, with a strong driving force and better through sexual; closed up garbage into the frame to avoid damage to machinery; key parts the use of the internationalization of procurement, in order to improve the intrinsic quality of the machine, thus greatly reducing the frequency of repair machinery; before the frame is equipped with auxiliary leveling shovel to push the level to unload solid filler; cab comfortable, all-sealed design, with have air-conditioning and heating and ventilation features have deodorant with anti-rollover protection device with a better operating environment; In order to facilitate the repair and maintenance, in the engine hood and the vehicle chassis set up a number of door and window repair; on both sides with spacious solid barrier for operators and maintenance personnel to provide a convenient platform for security.

XL26回填压实机主要特点是采用前后车架铰接连接，四轮独立液压驱动，具有极强的驱动力和较好的通过性；封闭式车架避免垃圾搅入而损坏机器；关键零部件采用国际化采购，以提高机器的内在品质，从而大大减少机器的维修频次；前车架上装有辅助整平铲，用以推平卸下的固体填料；驾驶室宽敞舒适、全密封设计，配有冷暖空调且有除臭换气功能，带有防翻滚保护装置，具有较好的操作环境；为便于维修保养，在发动机罩和车架上设置了多处门和维修窗口；两侧配有牢靠宽敞的护栏，为操作人员和维修人员提供了方便安全的平台。

METHODS: The level of intracellular calcium of human microglia grown on coverslip,which was loaded by calcium-probe,Fluo-4,and then treated in various experimental processing,was detected by confocal microscopy with time resolution mode.The binding of gp120 to human microglia was determined with confocal microscopy or flow cytometry after treatment with gp120 and stained with anti-gp120-FITC antibody.Phosphorylation of ERK within human microglia with or without gp120 stimulation was analyzed with confocal microscopy following the direct immuno-staining with anti-phosphorylated ERK antibody.

用钙离子探针Fluo-4标记粘附在盖玻片上的人小胶质细胞，运用共聚焦显微镜以荧光强度为指标实时观察各种条件下的细胞内钙离子水平的变化；用gp120处理并用anti-gp120-FITC进行染色，运用共聚焦显微镜术和流式细胞术分析人小胶质细胞与gp120结合情况；用抗磷酸化ERK 抗体免疫荧光方法进行染色，运用共聚焦显微镜术和流式细胞术进行ERK磷酸化水平分析。

The fusion DNA fragments of ag85b-mpb64 and ag85b-mpb64-esat-6 were obtained by PCR andSOE technique. Various DNA vaccines were constructed with the pcDNA3.1: fusion of two genes, and of three genes, bivalent combinations and trivalent combinations(pCA+pCM+pCE6). BALB/c mice were vaccinated with this DNA vaccines.The mice injected withBCG were positive control and the mice injected with pCDNA3.1 and PBS were negative control.The mice were immunized 3 times with 2-wk intervals. The animals in group BCG were only inoculatedsubcutaneously with 1×10~6 CFU BCG at initial vaccination. The serum IgG titers and IgG isotype weredetermined using iELISA coated with M. bovis PPD and rMAE protein expressed and depurated inprokaryotic expression system every week.

同样，利用PCR和SOE技术，获得牛分枝杆菌mpb64-ag85b和mpb64-ag85b-esat-6融合基因，以pCDNA3.1为载体构建了牛分枝杆菌多价组合和多基因融合DNA疫苗：二基因融合(pCDNA3.1-MPB64-Ag85B，简称pCMA)和三基因融合(pCDNA3.1-MPB64-Ag85B-ESAT-6，简称pCMAE)DNA疫苗；二价组合和三价组合(pCA+pCM+pCE6)DNA疫苗，免疫BALB／c小鼠，以牛分枝杆菌BCG免疫组为阳性对照，以pCDNA3.1及PBS免疫组为阴性对照，共免疫3次，每次间隔2周，BCG组仅初免时皮下免疫1次。1免后每周，以原核表达纯化的重组MPB64-Ag85B-ESAT-6蛋白和牛分枝杆菌PPD为包被抗原，以间接ELISA方法检测血清IgG水平及lgG亚类。

ASpheric FeNi nanoparticles with average diameter of about 70 nm were obtained in the system of cetyltrimethyl ammonium bromide/H_2O,while most of the products were nanofilms/rods with the addition of cyclohexane; nearly monodisperse FeNi nanoparticles with average diameter of about 25 nm were prepared in the system of PEG/cyclohexane/H_2O.With the assistance of ultrasonic,a no-surfactant method to 8.5 nm FeCo nanocrystals with high Ms(＞200.5 emu/g)has been developed with economical FeCl_3·6H_2O as iron sources.

a以水合肼为还原剂在十六烷基三甲基溴化铵/H_2O体系中得到了平均粒径约70 nm的FeNi合金球形颗粒，当在此体系中加入环己烷时样品主要形态为纳米膜/棒；于PEG/环己烷/H_2O体系中制备了单分散性较好的平均粒径约25 nm的FeNi合金纳米颗粒，合金纳米颗粒粒径随金属离子浓度减小而减小。

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。

However, as the name（read－only memory）implies, CD disks cannot be written onorchanged in any way.

然而，正如其名字所指出的那样，CD盘不能写，也不能用任何方式改变其内容。

Galvanizes steel pallet is mainly export which suits standard packing of European Union, the North America. galvanizes steel pallet is suitable to heavy rack. Pallet surface can design plate type, corrugated and the gap form, satisfies the different requirements.

镀锌钢托盘多用于出口，替代木托盘，免薰蒸，符合欧盟、北美各国对出口货物包装材料的法令要求；喷涂钢托盘适用于重载上货架之用，托盘表面根据需要制作成平板状、波纹状及间隔形式，满足不同的使用要求。