查询词典 activity

Instruments and so on. Being the phenomena of hard to avoid in human observation activity, observation activity, observational error plays an important role in the whole human coqnitive activity when it is bringing about huge negative effect, observational error, with the form of the "lesson by negative example". Stimulates and promotes human epistemic activity to more and more close to truth.

观察错误作为人类观察活动中一种难以避免的现象，在人类的整个认识活动中发挥着重要的作用，它在给人类带来巨大负面作用的同时，以一种"反面教材"的形式刺激并促进着人类的认识活动越来越接近于真理。

This thesis is formed by fives mainly, the first part recommends being covered with the state of development of mengniu milk industry, have drawn the advertising activity function performed in the course of covering with mengniu milk industry and developing; Second part Explain that is covered with the advertising strategic value that moves about of mengniu milk industry , sureness and realizing around the advertising strategic objective mainly, the strategy of the advertising activity draws up plans , advertising between activity and other relevant function close interdynamic , advertising activity " combining " such odd parts as function ,etc. is it expound the fact to launch in combining marketing of strategy.

本论文主要由五部分构成，第一部分介绍蒙牛乳业的发展状况，并引出了广告活动在蒙牛乳业发展过程中所起到的作用；第二部分阐述蒙牛乳业广告活动的战略价值，主要围绕广告战略目标的确定与实现、广告活动的战略运筹、广告活动与其它相关职能战略的密切互动、广告活动在整合营销中的"整合"作用等几部分展开论述。

In addition, NOS activity decreased with the time prolonged in vitro, when oxyhemoglobin, a scavenger of NO, was applied, the NOS activity kept stable. This result above demonstrated that NO can inhibit NOS activity, and it was the inhibition of NOS activity by NO that may be an important protective mechanism to resist the neurotoxicity by Py.

另外，本实验还发现，在体外实验时，一氧化氮合酶活性可随时间的延长而逐渐下降，当向反应体系中加入氧合血红蛋白去除一氧化氮的作用后，则一氧化氮的抑制作用消失，酶活性保持稳定；以上结果表明一氧化氮对于一氧化氮合酶活性具有抑制作用，而且这种抑制作用，可能是机体对抗拟除虫菊酯毒性作用的一种重要保护机制。

The results were as follows: the activity of prawns was highest under the condition of pH 7.0, 35 ℃ using pyrocatechol as substrate; four inhibitors i.e ascorbic acid1 mg·mL~(-1, sodium sulphite2 mg·mL~(-1, phytic acid1 mL·L~(-1 and EDTA0.1 mg·mL~(-1 had some inhibiting effects on the PPO of prawns, in which the effect of phytic acid1 mL·L~(-1 was the best; the PPO activity of prawns increased gradurally during the storage period; the PPO activity of prawns was inhibited in vacuum environment, the lower the storing temperature was, the stronger the PPO activity was.

结果表明：以邻苯二酚为底物，虾PPO活性的最适pH为7。 0，最适温度为35 ℃；4种抑制剂(1 mg·mL-1抗坏血酸、2 mg·mL-1亚硫酸钠、1 mL·L-1植酸及0。 1 mg·mL-1EDTA)对南美白对虾PPO都表现出一定的抑制作用，以1 mL·L-1植酸抑制作用最强；南美白对虾在贮藏过程中PPO活性逐渐上升，真空环境中PPO活性受到抑制，贮藏温度越低，抑制作用越强。

Since 70 time, the financial activity of 90 ％ above has concerned with commerce and investment activity not quite, it is to derive the acuteness growth that financial tool trades completely even, make financial activity breaks away from real economy activity increasingly and self-existent and move.

与西方国家的工业化历史发展相伴随的是经济的货币化进程。70年代以来，90％以上的金融活动已经与贸易和投资活动关系不大，甚至完全是为了衍生金融工具交易的剧烈增长，使金融活动日益脱离现实经济活动而独立存在和运行。

Little is known about the influence of minerals and other soil factors on the biocontrol activity of Trichoderma spp.The objectives of this study were to first evaluate the take-all–suppressive activity of T.koningii in field soils representative of the wheat-growing region in the Pacific Northwest of the United States,and then to identify abiotic edaphic parameters that are positively and negatively associated with the biocontrol activity of T.koningii in these soils.Such information will be usefulin selecting sites where T.koningii can be expected to perform optimally;in developing formulations that enhance biocontrol;and perhaps in indicating factors that favor mechanisms involved in the biocontrol activity of this strain such as antibiotic and enzyme biosynthesis.

知之甚少，对矿物和其它土壤因素对生物活性木霉镰刀本研究的目的首先评估全蚀抑制活性t.koningii土壤代表小麦种植区在西北太平洋的美国，然后找出生物土壤参数有积极和消极与生物防治活性t.koningii在soils.such这些信息将有助于在选择地点，可以t.koningii预计进入最佳状态；在发展制剂提高生物防治；或许说明因素，有利于参与机制，在生物防治活动，这株如抗生素和酶的合成。

objective to isolate and purify the antimicrobial peptides with anti-toxoplasma gondii activity isolated from the haemlymph of musca domestica larvae.methods the antimicrobial peptides of musca domestica larvae were induced by infection and injury were isolated and purified by trituration,centrifugalization and column chromatography.then the antimicrobial peptides with anti-toxoplasma activity were sieved by mtt colorimetric method and haemacytometry.results it was found that two antimicrobial peptides had anti-toxoplasma activity through resource s cationic column chromatography and superdex g75 gel column chromatography.conclusion the two antimicrobial peptides with anti-toxoplasma activity existing in the haemlymph of musca domestica larvae had different anti-toxoplasma effect.

作者单位：山西医科大学寄生虫教研室，太原 030001；化学生物学与分子工程教育部重点实验室山西大学生物技术研究所目的从家蝇幼虫血淋巴中分离纯化具有抗弓形虫作用的抗菌肽。方法通过损伤加感染的方法诱导家蝇幼虫大量表达抗菌肽，然后经过研磨、离心和层析等过程，将家蝇幼虫抗菌肽进行分离纯化，采用四甲基偶氮噻唑蓝比色法和血细胞计数法筛选对弓形虫速殖子有抑制作用的抗菌肽。结果经resource s阳离子柱和superdex g75凝胶柱层析后，筛选出2种对弓形虫速殖子有杀伤作用的抗菌肽。结论家蝇幼虫血淋巴中存在抗弓形虫作用的抗菌肽，而且不止一种，但其效果有所不同。

The results showed that there was a negative relationship between H2O2 content and CAT activity, thus H2O2 content was low when CAT activity was high. There was a close relationship between H2O2 content and differentiation process. H2O2 could be an important signal transduction factor during bud differentiation. IAA oxidase activity was decreased firstly, and then increased, which affected IAA oxidase and degradation pathway and regulate ratio of cytokinin and auxin. With differentiation process continuing, PPO activity was increased, which could cause browning or vitrifaction of seedling, or even malformation.

研究结果表明，鹅掌楸组培再生过程中，过氧化氢酶活性与H2O2含量变化呈负相关，CAT活性较高时，H2O2含量则较低。H2O2含量与鹅掌楸组培苗分化进程密切相关，H2O2可能作为信号因子在芽分化过程中发挥重要作用；IAA氧化酶活性呈现先下降后增加的变化规律，从而影响IAA氧化降解途径，调控细胞分裂素与生长素含量的比值，影响鹅掌楸芽的再生；PPO活性随培养时间的增加而升高，引起组培苗的褐变或玻璃化，甚至生长畸形。

Soil urease activity, sucrase activity, catalase activity and alkalescent phosphats activity reduced along with the soil layer.

随着农田的风蚀沙化，土壤中粉砂粒含量、有机质和养分含量急剧下降，中砂粒含量趋于增大。

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。

Who? I never heard of him, Paul said, before asking teammate James Posey if he had heard of him.

赛后，科比说，他一直都是一名非常出色的射手，今天他打得很棒。

When I joined the company, I rotated around the different sections.

我加入这个公司时，轮换过几个不同的部门。