检测

基本解释 (translations)

sense

与检测相关的网络例句 [注：此内容来源于网络，仅供参考]

It is the first important step in video analysis and will directly affects the effectiveness of indexing Shot boundary detection is one of our major research interests and we will tackle the following existing problems the ambiguity between gradual change and camera motion, the discontinuity during gradual change, false detection caused by illumination variation and flashlight, automatic threshold selection Firstly, we discuss shot boundary detection in non-compressed domain In chapter 2, we compare some of the commonly used detection methods which are based on frame difference and point out that single feature will not generate good results As a conclusion, we use fuzzy logic to combine multiple features Presently, most frame difference based shot boundary detection algorithms rely on threshold and hence the selection of such thresholds will greatly affect the performance of boundary detection We propose a membership function to define frame difference and calculate the membership with self adaptation according to the statistic distribution of frame differences to satisfy different type of video clips Experiments show that the proposed fuzzy shot boundary detection algorithm can be used with different video types and has a high detection precision and recall In chapter 3, we discuss model-based shot boundary detection algorithms regarding chromatic and spatial editing effects such as fade-in, fade-out, dissolve and wipe Various parameters are proposed to better describe the characteristics of each editing type.

镜头边界的检测是把视频自动地分割为一个个镜头，作为基本的索引单元，因此它是视频分析重要的第一步，直接影响到视频检索的成败。镜头边界的检测是本文研究的重点之一。目前镜头边界检测算法主要存在以下问题：渐变与镜头运动难以区别；渐变过程中的不连续与停顿、光照条件的变化及闪光灯等特殊情况会引起误检测；自动选择阈值比较困难等。本文首先针对非压缩域视频进行了镜头边界检测的研究。在第二章中我们采用了比较流行的基于帧间差的方法。在比较各种帧间差计算方法的基础上，指出使用单一的特征难以取得很好的检测效果，提出用模糊逻辑综合使用各种特征。目前大多数基于帧间差的镜头边界检测算法都采用阈值法进行镜头转换的判别。阈值选择的误差对检测性能有较大的影响，本文提出用隶属度函数定义帧间差较大、中等较大和较小等概念，并根据帧间差的统计分布自适应地确定隶属度，以适应不同类型的视频片断。实验结果表明这种基于糊逻辑的镜头边界检测算法可以适应不同的视频，并具有较高的检测精度和检出率。在第三章中采用基于模型的方法进行镜头渐变的检测，研究了淡入／淡出、慢转换和扫换的模型。

Company Profile Beijing Xinyu win equipment limited liability company operating mainly in the production and domestic and international advanced testing equipment, instrumentation, and diagnostic tools, as well as introduce advanced test, measurement of new technology for operating purposes. A: electrical fire, building fire detection and public safety facilities, equipment detectors B: lightning protection, lightning protection device detection equipment, mine detection device safety box C: Fire Fire Safety Inspection and Testing equipment, and investigate the cause of the fire equipment, police station fire alarm Services and equipment D: fire inspection and fire investigation equipment boxes, fire investigation kits, fire detection equipment to determine the scene Product E: Fire Engineering Detect boxes, cartons Detect building fire service installations, fire detection electrical box F: Airport Fire fire inspection equipment, subway Fire Safety Detect Box G: boilers, pressure vessels and special equipment, elevator equipment Detect H: Victoria seized power telecommunications equipment boxes, mechanical state patrol boxes I: Detect safety boxes, traffic accident investigation boxes, property management Detected me J: Public environmental hygiene Detect boxes, boxes of food safety at the scene detection, occupational health care at the scene Detect boxes, cartons Detect Radiological Protection at the scene, the situation of sanitation and disinfection Detected me, health production supervisor at the scene seized me K: Ultrasonic leak detector, ultrasonic spectrum analyzer, ultrasonic full-function fault detection system L: fire using infra-red thermal imaging, infrared imaging system for industrial use, the security-type infra-red thermal imaging M: Energy Conservation Supervision and Testing Instruments instrument N: Private Product: 3 1/2- 8 1 / 2 handheld / desktop Digital Multimeter, cross-DC clamp level pressure ammeter, temperature gauges, tachometer, digital megohm table, grounding resistance tester, desktop multimeter, digital frequency meter smart, figure synthesis / function signal generator, desktop digital electric bridge, oscilloscopes, infrared thermometer, vibrometer, digital DC regulated power supply, 5 1 / 2 hand-held multi-function calibrator field process instrumentation. O: agent Products:, infrared thermometer, infrared, ultrasonic full-function fault leakage / discharge detection device, flammable / toxic gas detector, harmonic power quality analyzer, portable ultrasonic flowmeter, insulation / Ground Resistance Tester, temperature, current / voltage, the process of signal, thermal resistance / thermocouple, pressure, loop calibrator, such as electronics, telecommunications, electricity, petroleum chemical industry, safety inspection, steel smelting, public environmental protection, fire detection Secret rescue, fire detection equipment, special equipment testing, military field equipment dedicated monitoring equipment and tools.

公司简介北京新宇胜利仪器有限责任公司主要以生产和经营国际，国内先进的检测仪器仪表和设备诊断工具以及介绍先进的测试，测量新技术为经营宗旨。A：消防电气、建筑消防设施检测和公共安全侦检仪器设备B：防雷、避雷装置检测仪器设备、防雷装置安全检测箱C：消防防火监督检测装备、火灾原因调查装备、公安派出所消防警务装备D：防火检查与火灾勘查仪器箱、火灾勘查工具箱、消防产品现场判定检测仪器E：消防工程检测箱、建筑消防设施检测箱、消防电气检测箱F：机场消防防火检查仪器设备、地铁消防安全检测箱G：锅炉、压力容器和特种设备、电梯检测仪器H：电信电源维检仪器箱、机械状态巡检箱I：交通安全检测箱、交通事故勘查箱、物业管理检测箱J：公共卫生环境检测箱、食品安全现场检测箱、职业健康监护现场检测箱、放射防护现场检测箱、卫生消毒状况检测箱、健康品生产现场监检箱K：超声波泄漏检测仪、超声波频谱分析仪、超声波全功能故障检测系统L：消防用红外热像仪、工业用红外热像仪、本安型红外热像仪M：节能监督检测仪器仪表工具N ：自有产品：3 1/2-8 1/2位手持/台式数字多用表，交、直流钳形高低、压电流表，温度仪表，转速表，数字兆欧表，接地电阻测试仪，台式多用表，数字智能频率计，数字合成/函数信号发生器，台式数字电桥，示波器，红外测温仪，测振仪，数字直流稳压电源，5 1/2位手持式多功能现场过程仪表校验仪。O：代理产品：，红外测温仪，红外热像仪，超声波全功能故障泄漏/放电侦测仪，可燃/有毒气体检测仪，电力质量谐波分析仪，便携式超声波流量计，绝缘/接地电阻测试仪，温度、电流/电压、过程信号、热电阻/热电偶、压力、回路校验仪等电子、通讯、电力、石油化工、安全检查、钢冶、公共环保、消防特勤侦检救援、消防检测设备、特种设备检测、军事领域的专用仪器监测设备与工具。

Compared with traditional invasion detection system has a lot of advantages to invade the detection system distributed: Distributed IDS is that a lot of measures the land to different data sources, adopts different measuring algorithms, measure together, cooperate and deal with, has improved the accuracy measured ; But distributed IDS can be used in the extensive network environment; Distributed IDS may use the special package to be punish and audit datum safely, help the system to be produced and invade the rule of measuring and produce and unusually measure models ; Distributed IDS analyses the behaviors of a lot of control points in coordination, may measure out and attack distributed in coordination ; The measuring of distributed IDS right a certain control point can be regarded as the early warning of other check points .

分布式入侵检测系统跟传统的入侵检测系统相比有很多优点：分布式IDS是多个检测域针对不同的数据来源，采用不同的检测算法，共同检测，协作处理，提高了检测的准确性；分布式IDS却可以用于大规模的网络环境；分布式IDS可以使用专门的组件处理安全审计数据，帮助系统生成入侵检测规则和生成异常检测模型；分布式IDS协同分析多个监控点的行为，就可能检测出分布式协同攻击；分布式IDS对某个监控点的检测可以作为对其他检测点的预警。

Firstly, electrization knowledge related to the research is introduced. After a deep study on various contact loss detection techniques, especially on the electric arcs detection techniques, we draw the conclusion that the untouched detection technique based on phototube sensor can acquire exact contact loss information, and will to be the leading technique for contact loss measurement in future. Secondly, combining with the special railways system in our country, we analyze the cause of the arcs, and the influence on the power supply system and the on board traction drive due to the arcs in detail, and study the arcs' spectrum characteristic. We also analyze detecting principles and put forward with a method - using phototube sensor to detect the contact loss arcs, conceive the configurations and detection flows of the measurement.

文章通过对电气化铁道相关知识的了解及对国内外离线检测技术的深入了解，尤其是对离线电弧检测技术的了解，总结出了基于光电传感器的非接触离线电弧检测系统能够得到准确的弓网离线情况，并且是国内外检测技术的发展方向；文章详细的分析了离线电弧产生的原因，电弧对机车牵引动力的影响情况，研究了我国铁路系统中离线电弧的光谱特征分布；分析了系统的检测原理，提出了采用光电传感器实现对离线电弧进行检测的方法，并设计了"电力机车弓网离线电弧检测装置"的检测功能和管理功能，规划了系统的组成结构及检测流程。

Thecompare of genetic map between Lowes and ours showed 26 homology marker situ,which occupied 21.1% of the marker situ in the experiment. 81 QTLs were detected for 11 agronomic traits. 4 QTLs were detected for plantheight, which explained 10.3%～28.9% of trait variance; 2 QTLs were detected forNo. of effective 1-st branches, which explained 22.1%～47% of trait variance; 16QTLs were detected for effective branches height, which explained 12.2%～51.8% oftrait variance; 15 QTLs were detected for length of main inflorenscence, whichexplained 7.4%～26.6% of trait variance; 5 QTLs were detected for effective siliquesof main inflorenscence, which explained 11.2%～25% of trait variance; 1 QTLs weredetected for density of main infiorenscence, which explained 17.3% of trait variance;12 QTLs were detected for length of silique, which explained 24%～36.7% of traitvariance; 2 QTLs were detected for seed per sillique, which explained 9.6% and16.9% of trait variance; 2 QTLs were detected for 1000 seed weight, which explained26%～13.7% of trait variance; 11 QTLs were detected for Total effective siliques perplant, which explained 14.8%～47.2% of trait variance; 11 QTLs were detected forplant height, which explained 14.3%～32.8% of trait variance.

其中，株高检测到4个QTLs，解释性状表型变异的10.3％～28.9％；一次有效分枝数检测到2个QTLs，解释性状表型变异的22.1％和47％；有效分枝部位检测到16个QTLs，解释性状表型变异的12.2％～51.8％；主花序长度检测到15个QTLs，解释性状表型变异的7.4％～26.6％；主花序有效角数检测到5个QTLs，解释性状表型变异的11.2％～25％；主花序角密度检测到1个QTLs，解释性状表型变异的17.3％；角果长度检测到12个QTLs，解释性状表型变异的24％～36.7％；每角粒数检测到2个QTLs，解释性状表型变异的9.6％和16.9％；千粒重检测到2个QTLs，解释性状表型变异的26％和13.7％；单株有效角果总数检测到11个QTLs，解释性状表型变异的14.8％～47.2％；单株产量检测到11个QTLs，解释性状表型变异的14.3％～32.8％。

Get high purity DCs by Cultured plastic-adherent monocytes isolated from healthy human peripheral blood with GM-CSF and IL-4 for 7 days. To observe the morphology of DCs by inverted phase contrast microscope ,electron microscope and laser confocal microscope. Analyse phenotype of DCs with flow cytometry. Investigate the endocytosis ability of DCs as a group by Horseradish peroxidase endocytosis assay. To appraise allogeneic mixed lymphocytes reaction of DCs by MTT reduction assay. Analyse the levels of IL-12 and TNF in liquids of cultured medium by ELISA and MTT reduction assay respectively. Soluble antigens of HCCs was obtained by 3 freeze-and-thaw cycles. Biological characteristics of HC soluble antigens pulsed DCs were monitored by flow cytometry. According to MTT reduction assay estimated the cell proliferation of self lymphocytes activated by HC antigens pulsed DCs. Get high purity BCG HSP 70 protein by SDS-PAGE electrophoresis and determined its biological activity with ELISA. Analyse phenotype of antigen pulsed DCs primed by BCG HSP70 with flow cytometry. By MTT reduction assay estimated the cell proliferation of self lymphocytes and the MLR of DC based vaccine. Analyse expression of HLA-DR molecule on surface of HCC lines. The IFN-γ mRNA in lymphocytes after actived by DC vaccine and the Fas-L expression on DC and DC vaccine primed lymphocytes were detected by in situ hybridization and flow cytometry respectively. Specific cytotoxity lysis of T lymphocytes and nonspecific inhibition of liquids in culture medium against HCC lines were also tested. Detect expression of hAFP on four HCC lines with Cell-ELISA. Induce apoptosis of HCCs with actinomycin-D. Interaction of DCs and apoptotic cells was observed under transmission electron microscope. Growth inhibition test of DC against HCC lines was also performed. Establish the nude mouse model bearing human HC xenografts and indentify the characteristic of tumour by histochemistry and immunohistochemistry techniques. Prevent and treat transplanted human HC on nude mouse with Freezing and anabiotic HC specific lymphocytes.

用GM-CSF和IL-4从健康人外周血诱导DC；分别用倒置相差显微镜、电子显微镜及激光共聚焦显微镜观察DC形态；流式细胞术检测DC表型；HRP吞噬实验测定DC的群体内吞能力；MTT法检测同种异体混合淋巴细胞反应；ELISA法和MTT法分别测定DC培养上清液中IL-12和TNF水平；冻融法制备肝癌细胞可溶性抗原；流式细胞术检测负载肝癌可溶性抗原后DC的生物学特性；MTT法检测DC负载肝癌抗原后对自身淋巴细胞增殖的影响；SDS-PAGE制备电泳纯化BCG HSP70并鉴定纯度，ELISA测定活性；流式细胞术检测负载抗原DC经BCGHSP 70活化后的表型；MTT法检测肝癌DC疫苗对自身淋巴细胞增殖的影响和混合淋巴细胞反应；流式细胞术检测肝癌细胞表面HLA-DR表达；MTT法检测肝癌DC疫苗对自身淋巴细胞的活化；原位杂交法检测肝癌DC疫苗活化后的淋巴细胞IFN-γmRNA表达；流式细胞术检测DC和肝癌DC疫苗活化后淋巴细胞表面Fas-L；MTT法分别检测肝癌DC疫苗活化的淋巴细胞和其培养上清对肝癌细胞的特异性杀伤和非特异性抑制作用；Cell-ELISA检测人肝癌细胞hAFP表达；MTT法检测负载AFP表位肽和凋亡肝癌细胞DC对自身淋巴细胞增殖的影响；ELISA法和MTT法分别测定活化后淋巴细胞培养上清中TNF和IL-12水平；肝癌细胞凋亡的诱导和检测；DC吞噬凋亡肝癌细胞后的电子显微镜观察；DC对肝癌细胞的生长抑制试验；人肝癌裸鼠皮下移植瘤动物模型的建立及其组织学和免疫组织化学鉴定；DC及肝癌特异性淋巴细胞预防和治疗人肝癌裸鼠皮下移植瘤；冻存和复苏后的肝癌特异性淋巴细胞预防和治疗人肝癌裸鼠皮下移植瘤。

The stable clones are further identified by RT-PCR and Western blot; 6 MTT assay is used to investigate the effect of ZNRD1 on the cell growth of cells (AGS, SGC7901, MKN28, NIH3T3, GES-1); 7 Soft agar assay is used to investigate the effect of ZNRD1 on the clonality of cells (AGS, MKN28); 8 Nude mice assay is used to investigate the effect of ZNRD1 on the cell growth of gastric cancer cells (AGS, MKN28); 9 Flow cytometry is used to investigate the effect of ZNRD1 on the cell cycle distribution of cells (AGS, MKN28, NIH3T3, GES-1); 10 Flow cytometry is used to investigate the effect of ZNRD1 on the cell apoptosis of cells (AGS, MKN28, NIH3T3); 11 MTT assay is used to investigate the effect of ZNRD1 on the drug sensitivity of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR) in vitro; 12 SRCA is used to investigate the effect of ZNRD1 on the drug sensitivity of gastric cancer cells (SGC7901, SGC7901/VCR) in vivo; 13 Flow cytometry is used to investigate the effect of ZNRD1 on adriamycin accumulation of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR); 14 Transmission electron microscope is used to investigate the effect of ZNRD1 on the sensitivity of SGC7901 cells towards drug-induced apoptosis; 15 Flow cytometry and DNA ladder assay are used to investigate the effect of ZNRD1 on the sensitivity of cells (SGC7901, SGC7901/VCR, HL-60/VCR) towards drug-induced apoptosis; 16 Microarray is used to investigate the profiling of ZNRD1-responsive genes in gastric cancer cells (AGS, MKN28, SGC7901, SGC7901/VCR); 17 RT-PCR and Western blot are used to identify the results of microarray; 18 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of cyclin D1; 19 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of MDR1; 20 Kinase assay is used to investigate the effect of ZNRD1 on the activity of cyclin E-CDK2 kinase; 21 The antisensenucleic acids of p21 is used to inhibit the expression of p21, and flow cytometry is used to investigate the effect of p21 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 22 The antisensenucleic acids of p27 is used to inhibit the expression of p27, and flow cytometry is used to investigate the effect of p27 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 23 Liposome is used to up-regulate the expression of Skp2, and flow cytometry is used to investigate the effect of Skp2 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 24 Western blot is used to investigate the effect of ZNRD1 on the stability of Skp2 and p27 in gastric cancer cells; 25 MVD assay is used to investigate the effect of ZNRD1 on the angiopoietic activity of gastric cancer cells; 26 ELISA is used to investigate the effect of ZNRD1 on the expression of VEGF165 in gastric cancer cells; 27 The roles of DARPP-32 in MDR of gastric cancer cells are investigated using gene transfection, MTT assay, SRCA, flow cytometry and DNA ladder assay.

应用杂交瘤技术制备ZNRD1的首个单克隆抗体；2）利用RT-PCR、Western blot和免疫组化检测ZNRD1在胃癌组织、胃炎组织、正常胃上皮组织、胃癌细胞和正常胃组织上皮细胞中的表达；3）构建ZNRD1的小干扰RNA载体，并测序鉴定；4）利用脂质体将ZNRD1的真核表达载体及其空载体转染胃癌细胞（AGS、SGC7901、MKN28）和小鼠成纤维细胞（NIH3T3），G418筛选后进行鉴定；5）利用脂质体将ZNRD1的小干扰RNA载体及其空载体转染药敏胃癌细胞（SGC7901）、正常胃组织上皮细胞（GES-1）、对长春新碱耐药的胃癌细胞（SGC7901/VCR）、药敏白血病细胞（HL-60）、对长春新碱耐药的白血病细胞（HL-60/VCR），G418筛选后进行鉴定；6）利用MTT实验检测ZNRD1高/低表达对细胞（AGS、SGC7901、MKN28、NIH3T3、GES-1）生长的影响；7）通过软琼脂克隆形成实验检测上调ZNRD1对AGS、MKN28细胞克隆形成能力的影响；8）通过裸鼠成瘤实验检测上调ZNRD1对AGS、MKN28细胞体内成瘤性的影响；9）通过流式细胞仪分析ZNRD1高/低表达对细胞（AGS、MKN28、NIH3T3、GES-1）的细胞周期的影响；10）通过流式细胞仪分析上调ZNRD1对细胞（AGS、MKN28、NIH3T3）的凋亡的影响；11）通过MTT实验检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60、HL-60/VCR）体外药物敏感性的影响；12）通过肾包膜下移植法检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR）体内药物敏感性的影响；13）通过流式细胞仪分析ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60、HL-60/VCR）内阿霉素蓄积和泵出的影响；14）通过透射电镜检测上调ZNRD1对SGC7901细胞凋亡敏感性的影响；15）通过流式细胞仪和DNA梯度试验检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60）凋亡敏感性的影响；16）通过基因芯片检测ZNRD1高/低表达对胃癌细胞内基因表达谱的影响；17）利用RT-PCR、Western blot对基因芯片的结果进行鉴定；18）利用报告基因实验检测ZNRD1对cyclin D1的启动子活性的调节作用；19）利用报告基因实验检测ZNRD1高/低表达对MDR1的启动子活性的调节作用；20）利用激酶试验检测ZNRD1对cyclin E-CDK2 激酶活力的影响；21）利用反义核酸技术抑制p21的表达；通过流式细胞仪检测抑制p21对ZNRD1介导的细胞周期阻滞的影响；22）利用反义核酸技术抑制p27的表达；通过流式细胞仪检测抑制p27对ZNRD1介导的细胞周期阻滞的影响；23）利用脂质体转染法上调Skp2的表达；通过流式细胞仪检测上调Skp2对ZNRD1介导的细胞周期阻滞的影响；24）利用Western blot检测ZNRD1对p27和Skp2的蛋白稳定性的影响；25）利用微血管密度实验检测ZNRD1对AGS、MKN28细胞裸鼠移植瘤微血管形成的影响；26）利用ELISA检测ZNRD1对AGS、MKN28细胞培养上清和移植瘤匀浆中VEGF165含量的影响；27）利用脂质体转染法、MTT实验、肾包膜下移植法、流式细胞仪和DNA梯度试验检测新耐药相关分子DARPP-32对细胞（SGC7901、SGC7901/VCR、对阿霉素耐药的胃癌细胞SGC7901/ADR）多药耐药表型的影响；利用脂质体转染法和MTT实验检测下调ZNRD1对DARPP-32介导的胃癌多药耐药的调控作用。

The essence of EDID is to set up a normal behavior fuzzy sub collection A on the basis of watching the normal system transfer of the privilege process, and set up a fuzzy sub collection B with real time transfer array, then detect with the principle of minimum distance in fuzzy discernmethodThe innovation point of this paper is : Put forward the method of EDID, can not only reduce efficiently false positive rate and false negative rate, also make real time intrusion detection to become possibility; have independent and complete character database, according to the classification of monitoring program, design normal behavior and anomaly behavior etc., have raised the strongness of IDS; Use tree type structure to preservation the character database, have saved greatly stock space; in detection invade , carry out frequency prior principle, prior analysis and handling the behavior feature of high frequency in information table, have raised efficiency and the speed of detection, make real time intrusion detection to become possibility; have at the same time realized anomaly intrusion detection and misuse intrusion detection, have remedied deficiency of unitary detection method.

本文的创新点是：通过对特权进程的系统调用及参数序列的研究，提出了基于Euclidean距离的入侵检测方法EDID，不仅能有效降低漏报率和误报率，而且使实时入侵检测成为可能；设计有独立而完整的特征数据库，根据被监控程序的类别，分别设计正常行为、异常行为等，提高了检测系统的强健性和可伸缩性；特征数据库按树型结构存储，大大节省了存储空间；在检测入侵时，实行频度优先原则，优先分析和处理信息表中的高频度行为特征，提高检测的速度和效率，使实时入侵检测成为可能；同时实现了异常入侵检测和误用入侵检测，弥补了单一检测方法的不足。

4 Results of nondestructive test for weld joints shall be graded according to JB 4730. Following requirements shall be met: a For radial test, quality grade of radial transillumination can't be lower than Grade AB, and that of weld joints shall meet table 10; b For supersonic test, approval standard for weld joints are as follows: 1 For weld joints of 100% supersonic test, grade Ⅰ. 2 For weld joints of local supersonic test, grade Ⅱ. c For magnetic particle test and penetration test, grade Ⅰ.

7.5.4 管道焊接接头的无损检测应按 JB 4730 进行焊缝缺陷等级评定，并符合下列要求： a 射线检测时，射线透照质量等级不得低于 AB 级，焊接接头经射线检测后的合格等级应符合表 10 的规定； b 超声波检测时，管道焊接接头经检测后的合格标准如下： 1 规定进行 100%超声波检测的焊接接头 I 级合格； 2 局部进行超声波检测的焊接接头 II 级合格； c 磁粉检测和渗透检测的焊接接头 I 级合格。

One pair of primers that amplified the gB gene of pseudorabies viruswas designed and synthesized.PCR technique detecting the DNA of PRV was established after selecting the best reaction conditions.This technique was applied to specifically amplify the 281 bp DNA fragment of the PRV strains including Fa,Fb,Bartha,BJ,GD,V2F4,S,S3,SR,Buk,Shope,Norden,Mink Ⅲ,HB,F8,F9 and F12 in cultured samples.The negative results were achieved from Vero cells,swine vesicular disease virus,hog cholera virus,Japanese encephalitis virus,porcine reproductive and respiratory syndrome virus,porcine parvovirus,foot and mouth disease virus F29 strain,O3I3 strain,T509 strain and O Ⅱ MF249 strain.The results of sequencing showed that the PCR method was of specificity.The sensitivity of PCR reached 15.8 pg of PRV Fa strain DNA.The tissue samples obtained during 1994 and 2000 were detected,and the results showed that the sensitivity of PCR was more sensitive than virus isolation and the Sandwich ELISA.The PCR was applied to detect 191 tissue samples from 31 pig farms obtained from Guangdong,Fujian,Hainan Provinces during 1999 and 2000,50 samples(26.2%)were positive and 22 pig farms(71%)were positive.

根据伪狂犬病病毒gB基因的序列，设计并合成了一对引物，以闽A株细胞培养毒为模板，筛选最佳反应条件，建立了检测PRV的PCR方法应用该方法对Fb、Bartha、BJ、GD、V2F4、S、S3、SR、Buk、Shope、Norden、MinkⅢ、HB、F8、F9、F12等毒株的细胞培养液进行基因扩增，均获得了分子量为 2 81bp的特异性目的DNA片段，而对Vero细胞与FMDV、SVDV、HCV、PRRSV、JEV、PPV等病毒进行检测，结果均为阴性，没有出现交叉反应对PRV毒株扩增的产物测序，结果序列与文献报道一致，证明PCR扩增产物和方法的特异性对 1994～ 2 0 0 0年期间送检的临床样品和保存的PRV毒种，用病毒分离、双抗体夹心ELISA和PCR等 3种方法进行检测，结果前 2种方法检测为阳性的，PCR检测均为阳性；PCR检测为阴性，前 2种方法检测也为阴性；可是，前 2种方法检测为阴性的，PCR却检测出部分阳性；经x2 检验，证明PCR检出率明显高于前 2种方法的检出率对PRV闽A株细胞毒提取物DNA进行检测，其最低检出量为 15 8pg 对 1999～ 2 0 0 0年期间广东、福建、海南等省的 31个大中型猪场送检的 191份病料进行检测。

与检测相关的网络解释 [注：此内容来源于网络，仅供参考]

Androsterone test system：雄甾酮检测系统

862.1075 雄(甾)烯二酮检测系统 Androstenedione test system | 862.1080 雄甾酮检测系统 Androsterone test system | 862.1085 血管紧缩素I 和肾素检测系统 Angiotensin I and renin test system

automatic error correction/detection,AECD：自动错误校正/检测

自动错误校正/检测 automatic error correction/detection,AECD | 自动错误检测 automatic error dection | 自动错误检测 automatic error detection

detectability：可检测性;能检测性;检测能力

destination,目的站 | detectability,可检测性;能检测性;检测能力 | detecting instrument,检出器;检测元件;检波器

detectable element：検出可能要素,可检测象素,可检测元素,可检出元素

detectable 可検出 | detectable element 検出可能要素,可检测象素,可检测元素,可检出元素 | detectable group 可检测象素组,可检测组,可检出组

detected signal：已检测信号,被检测信号

可侦测性因子 detectability factor | 已检测信号,被检测信号 detected signal | 检测,侦测,检波 detection

Nondestructive test：无损检测

无损检测(nondestructive test)简称NDT. 人们常常用手拍击西瓜判断是否成熟,检车工敲击车轴检查机车车轮是否能安全运行;医生用扣诊的方法诊断病情. 这些都是常见的"无损检测". 无损检测就是不破坏和损伤受检物体,对它的性能、质量、有无内部缺陷进行检测的一种技术. 工业上

UT：超声检测

射线照相检验(RT)、超声检测(UT)、磁粉检测(MT)和液体渗透检测(PT) 四种. 其他无损检测方法:涡流检测(ET)、声发射检测(ET)、热像/红外(TIR)、泄漏试验(LT)、交流场测量技术(ACFMT)、漏磁检验(MFL)、远场测试检测方法(RFT)等.

detecting instrument：检出器;检测元件;检波器

detectability,可检测性;能检测性;检测能力 | detecting instrument,检出器;检测元件;检波器 | developer,显示剂

Detects：检测的检测项目信息

检验的检测项目信息Examines; | 检测的检测项目信息Detects; | 检测的整车指标数据信息Targets;

Examines：检验的检测项目信息

车辆检测项目判定结果表Assess; | 检验的检测项目信息Examines; | 检测的检测项目信息Detects;