e-e reaction 中文意思是什麼

e-e reaction 解釋
紅斑水腫性反應, 福謝氏反應
  • e : （pl E s e s ）1 英文字母表第五字母。2 【音樂】E調，E音。3 E字形。4 〈美國〉（順序）第五等，（成...
  • reaction : n 1 反作用，反應；反沖；反動力。2 【政治學】反動，倒退；復古（運動）。3 【化學】反應，【物理學】...
  1. A wide variety of natural products, e. g. alkaloids, - lactames, biotin, amino sugars has been synthesized by 1, 3 - dipolar cycloaddition reaction between nitrones and alkenes

    通過硝酮與烯烴化合物的1 ， 3 -偶極環加成反應合成了許多天然?物，如生物鹼、 -內酰胺、生物素、氨基糖等。
  2. Abstract : a wide variety of natural products, e. g. alkaloids, - lactames, biotin, amino sugars has been synthesized by 1, 3 - dipolar cycloaddition reaction between nitrones and alkenes

    文摘:通過硝酮與烯烴化合物的1 ， 3 -偶極環加成反應合成了許多天然產物，如生物堿、 -內酰胺、生物素、氨基糖等。
  3. In this paper, 45 e. coli strains isolated from chicken farms in sichuan province were determined to be the pathogenic e. coli by animal test. type 1 pili of 45 strains isolated was detected by msha. the pila gene of 45 avian pathogenic e. coli strains were amplified by the polymerase chain reaction ( pcr ) with primers designed according to the sequence of the pila gene in genbank. results showed that pcr was more sensitive, faster and more characteristic than msha to detect type 1 pili

    本研究將從四川規模化雞場分離鑒定、經1日齡雛雞致病性試驗得到的雞源致病性大腸桿菌45株，採用d -甘露糖敏感血凝試驗（ msha ）檢測1型菌毛，根據genbank中公布的人源大腸桿菌1型菌毛pila基因序列設計一對引物用pcr擴增雞源致病性大腸桿菌1型菌毛pila基因。
  4. To study on structure and inheritance of rh d gene interaction between gene expression of rh d and rh c / e and influences on rh d gene expression of inserts and rh box - methods : 20 pairs of oligonucleotide specific primers for exon, intron 2 4, insert and rh box of rh d, rhc / e gene were designed and composed the polymerase chain reaction - sequence specific oligonucleotide primer ( pcr - ssp ) was used to amplify the rh c / e gene, rh d gene, exon, intron, insert and rh box in 106 samples of unrelated individuals and 7 han nationality ancestries and 5 wei nationality ancestries whose proband were rh d - negative

    目的：觀察中國漢族非血緣關系隨機個體、漢族及維吾爾族家系rh血型的c e基因、 d基因外顯子、內含子、插入片段以及rhbox ，研究rhd基因結構及遺傳規律， d基因表達與c e基因的關聯，以及插入片段和rhbox對d基因表達的影響。
  5. In macrosopic theories of foreign direct investment, author mainly describes g. damacdougall ' s international investment benefit distribution, kiyoshi kijima ' s theory of comparative superiority investment, r. aiiber ' s theory of money area, john dunning ' s theory of investment development stratege. in microsopic theories of foreign direct investment, author describes stephen herbert hymer & charles p. kindlebeger ' s toheory of monopolization - superiority, teter j. buckley & mark c. casson ' s internalization special advantage theory, raymond vernon " product circle theory, e. f. heckscher & b. ohlin " locational choice advantage theory, john dunning ' s compromise theory of international product. section 3 analyzes current enterprise intemationization theories which involves theories and model such as uppsala international model ( u - m ), cavugil ' s export behavior theory, international operation driving theory, hagg & johnson, etc. 1 enterprise intemationization network model, rogers ' s the innovating - related intemationization models ( i - m ), prahalard & doz ' s integration and reaction model, farmer, r. n

    在外國直接投資的宏觀理論中，主要論述了麥克道格爾（ g . d . a . macdougall ）的國際投資利益分配模型；小島清（ kiyoshikojima ）的比較優勢投資理論；阿利伯（ r . aliber ）的貨幣區域理論；鄧寧（ johndunning ）的投資發展階段理論；在外國直接投資的微觀理論中，重點討論了海默（ stephenherberthymer ）和金德爾伯格（ charlesp . kindlebeger ）等人的壟斷優勢理論；巴克利（ peterj . buckley ）和卡森（ markc . casson ）等人的內部化理論；弗農（ raymondvernon ）的產品周期理論；赫克歇爾（ e . f . heckscher ）和俄林（ b . ohlin ）的區位理論；鄧寧（ johndunning ）的國際生產折衷理論。
  6. If the stimulation i. e., the drug - taking course lasts too long, things will go to the opposite. b cells reaction will decline from excitement to paralysis. with declining functions, their release of insulin will become less and less

    而且刺激時間過長即服藥時間過長，那麼，物極必反，由興奮到麻痹， b細胞生理功能益趨衰退，胰島素分泌量越會減少。
  7. The results can be used to accurately extract the nuclear matrix of the astrophysically significant 7be + e - - 7li + v reaction. the method we used may find important application in condensed matter physics

    這一結果可用於精確抽取在核天體物理中有重要意義的反應7be + e - 7li + v的原子核矩陣元。
  8. The research shows that students misunderstand the relation between force and motion. gravity and action / reaction ; that in dc circuit, students of different age groups have the belief of " consumption of current ", " clashing currents " and " the battery as a constant current generator " ; that in understanding the concepts of electricity students lack th e knowledge of relating the micro with the macro ; and that students have serious difficulties in understanding the propagation of mechanics wave, the speed of wave and superposition, and do not make a distinction between the initial conditions and the medium properties of the system

    具體表現在：學生對力和運動的關系、重力和平衡、作用力與反作用力存在一些誤解；對直流電路，不同年齡的學生不同程度地存在電流消耗、碰撞電流、恆定電流源等觀念，而且對電學概念的理解缺乏宏觀與微觀的聯系；學生在機械波的傳播、波速、波的疊加上存在嚴重的困難，對于機械波的傳播學生不能區分初始條件和媒質特性，並錯誤地將動力學某些觀念與機械波進行類比。
  9. On march 8, real - time polymerase chain reaction orthopoxirus generic assay and nonariola orthopoxirus assay were positie for orthopoxirus dna, supporting the clinical diagnosis of e, and the diagnosis of accinia was confirmed at the us centers for disease control and preention

    3月8日，實時聚合酶鏈反應痘苗病毒屬測定和非天花痘苗病毒屬測定痘苗病毒屬dna是陽性，支持牛痘性濕疹的臨床診斷，並且美國疾病控制與預防中心也證實了牛痘的診斷。
  10. By adopting the iodide - iodate reaction system as an index, the distribution of segregation index ( x ) along the radial direction of packing and the effects of different operational conditions ( e. g. rotational speed, flow rates ) on micromixing efficiency of a novel rotating packed bed ( rpb ) have been investigated

    通過設計一臺能實現沿程取樣的旋轉填充床，同時通過採用一種平行競爭微觀混合體系碘化物碘酸鹽反應體系，考察了填料的不同徑向位置離集指數的分佈及各操作參數對旋轉填充床微觀混合效率的影響。
  11. Abstract : aim to synthesize a new prodrug, resveratrol trinicotinate. methods in presence of lithium and a catalytic amount of naphthalene, the reaction of p - methoxybenzyl trimethylsilyl ether and 3, 5 - dimethoxylbenzaldehyde gave resveratrol after a series of translation. resveratrol trinicotinate was obtained by the reaction of resveratrol and nicotinoyl chloride hydrochloride. results a mutual prodrug resveratrol trinicotinate was designed and synthesized. conclusion a novel method for synthesis of resveratrol and resveratrol trinicotinate has been afforded. the e - isomer is selectivily obtained by dehydration of the compound 2 with khso4

    文摘:目的合成一種前藥白藜蘆醇煙酸酯.方法在金屬鋰片和催化量的萘的存在下， 3 ， 5 -二甲氧基苯甲醛與對甲氧基苯甲醇的三甲基硅醚反應經過一系列轉變得到白藜蘆醇，白藜蘆醇與煙酰氯反應得到白藜蘆醇煙酸酯.結果設計併合成了白藜蘆醇煙酸酯.結論提供了一種合成白藜蘆醇及白藜蘆醇煙酸酯的方法，採用khso4脫水可選擇性的得到反式產物
  12. In this study, we designed a pair of primers based on the sequence of the upstream and downstream of chicken il - 2 gene. about 600 bp chicken il - 2 cdna fragment was cloned from cona - stimulated chicken splenocytes by reverse transcription - polymerase chain reaction ( rt - pcr ) and was subcloned into puc18 vector. recombinant clone was demonstrated by restriction enzyme digestion and dna sequencing. next, we construct recombinant plasmid pproex ? t - il - 2. the cdna of chicken il - 2 gene was subcloned into bamh i / hind iii sites of vector. the recombinant plasmid pproex ? t - il - 2 was transformed into e. coli dh5a and the bacteria was induced with iptg. it was demonstrated by sds - page and western blot that a 18kda protein which was equal to chicken il - 2 protein in molecular weight was expressed in e. coli dh5a. the expression level was up to 30 % of the total bacterial proteins. the purified protein was used to prepare the antibody against chicken il - 2 protein

    經酶切鑒定及dna序列測定，該基因為雞il - 2基因，其序列與sundick等報道的完全一致。在此基礎上，我們把雞il - 2基因亞克隆到大腸桿菌原核表達載體pproex ~ （ tm ） ht中，構建重組表達質粒並進行確證性序列測定，重組質粒測序結果表明將編碼雞il - 2成熟蛋白的基因正確地插入到原核表達載體pproex ~ （ tm ） ht的目的位點。重組質粒轉化受體菌dh5後用iptg於37進行誘導培養， sds - page和westernblot分析顯示，表達的雞il - 2融合蛋白分子量約為18kda ，表達的融合蛋白經薄層掃描發現目的蛋白表達量約占菌體蛋白的30 。
  13. Ptxb1 - hng and ptxb1 - m - insulin are expressed in e. coli successfully. after sds - page and densitometric scan analysis, the results show that the expression level of hng fusion protein is above 40 % and m - insulin fusion protein above 50 % of total bacterial proteins. western - blot result demonstrated m - insulin fusion protein had specific reaction with mouse anti human insulin antibody ( igg )

    Pbv220 ? hng在大腸桿菌中未檢測到表達，后兩個克隆在大腸桿菌bl21 （ de3 ）中獲得高效表達， hng及m - insulin融合蛋白表達量分別佔全菌蛋白的40及50左右；經western - blot鑒定m - insulin融合蛋白可以與小鼠抗人胰島素單克隆抗體（ igg ）發生抗原抗體結合反應。
  14. Purpose 1 construction of prokaryotic high expression vector of human platelet factor 4 ( h pf4 ) 2 expression and purification of r h pf4 3 bioassay of r h pf4 methods according to the modulation character of eukaryotic protein expression in prokaryotic cells, we design a pair of particular primers, and construct a prokaryotic expression vector pbv220 - r hpf4 by dna polymerase chain reaction ( pcr ) and dna recombinant technic. the expression plasmid was identified with pcr and dna sequencing. pbv220 - r hpf4 was transformed into e. coli dh5a, bl21 ( de3 ) and induced by increasing the temperature to 42. we identified the expression protein by sds - page and western - blotting

    目的1人血小板因子4 （ hpf4 ）原核高效表達克隆的構建2重組hpf4的表達及分離、純化工藝研究3重組hpf4的特性研究方法根據原核細胞表達真核蛋白的基因表達調控特點，設計合成一對特異引物，在pt7 - 7 - rpf4表達質粒的基礎上，應用聚合酶鏈式反應（ pcr ）對其cdna進行改造，通過dna重組技術構建成重組hpf4原核表達質粒pbv220 - rhpf4 ，用快速pcr檢測法、 dna測序分析，鑒定重組hpf4表達質粒的正確性。
  15. In this experiment hcv structural gene was amplified by polymerase chain reaction ( pcr ), and was inserted into baculovirus expression vector pfastbacl to construct a recombinant transposing vector pfbl - cee. the plasmid pfb 1 - cee was transformed into dh1 obac competent e. coli cells. high molecular weight dna was prepared from the overnight cultures from the selected e. coli colonies, which was recombinant baculovirus shuttle vector containing hcv structural gene, named bac - cee

    本實驗用pcr擴增hcv結構區基因，克隆到桿狀病毒表達載體pfastbacl中，構建成重組轉座載體pfb1 - cee ，轉化dh10bac大腸桿菌感受態細胞，篩選陽性菌落，抽提大分子質粒dna ，獲得含hcv結構區基因的重組桿狀病毒穿梭載體bac - cee ，脂質體介導轉染sf9昆蟲細胞，出現細胞病變后，收集含有重組桿狀病毒顆粒的培養上消，重新感染sf9細胞，收集sf9細胞，進行12 . 5 sds -聚丙烯酰胺凝膠電泳，可見表達的蛋白條帶。
  16. In order to understand the epidemiological behaviors of this pathogen, we studied strains e. coli 0157 isolated from patients and dung beetles in 1999 and 2000 in xuzhou city, jiangsu province, by methods of pcr, antimicrobial susceptibility, biochemical reaction and pfge ( pulse - field gel electrophoresis ) of chromosomal dna digested by restriction enzyme xbal

    為了探索我國大腸桿菌o157 ： h7感染的流行病學特點，我們使用了聚合酶鏈反應、生化反應、抗生素敏感實驗、脈沖電場凝膠電泳等分子生物學方法，對我國1999 - 2000年徐州地區分離到的部分大腸桿菌o157 ： h7進行了分析。
  17. In order to further investigate the role of axudl in human tumor carcinogenesis and the potential association between the axudl gene expression status and the stimulation of transforming growth factor beta in human cancers, the present study was performed in three aspects as follows : ( 1 ) cloning full length enconding region cdna of axudl and construction of eukaryotic vector that expression the fusion protein of axud1 and influenza virus hemagglutin ha epitope tag ; ( 2 ) exploring the time and dose effects of tgf - 1 on the expression - of axudl gene in hepg2 hepatoma cells and spc - a1 lung carcinomas cells, and studying the effects of overexpression of axud1 on the expression of cell cycle and apoptosis related protein in hepg2 hepatoma cells ; ( 3 ) construction and expression of human axudl in e. coli m15. the following main results and conclusions can be obtained from the present study : 1. the full length ecnoding region of human axudl cdna from human peripheral blood lymphocytes was successfully cloned using one step rt - pcr method, and constructed into a eukaryotic expression vector which can be expressed a ha - axud1 fusion protein with axud1 and influenza virus hemagglutin ha epitope tag. the recombinant plasmid was identified by polymerase chain reaction, restriction endonuclease maping and sequencing, this expression vector might be instrumental to further study the function of axud1 protein in tumor cells

    為了進一步研究axud1在人類腫瘤發生中的作用及axud1基因的表達狀況與tgf -介導的信號通路的關系，本實驗研究分為三個部分： （ 1 ） axud1基因cdna全長編碼區的克隆和ha表位標記的axud1基因表達載體的構建； （ 2 ）探討肝癌細胞hepg2和肺腺癌spc - a1細胞中tgf - 1誘導的axud1基因表達的時間、劑量效應以及誘導表達的可能機理，並研究axud1的過表達對細胞周期和細胞凋亡相關蛋白表達的影響； （ 3 ） axud1原核表達載體的構建及其在大腸桿菌中的表達。本實驗的主要結果和結論如下： 1利用一步法rt - pcr成功地從人類外周血淋巴細胞中克隆出axud1基因編碼區cdna ，並將其構建入真核表達載體中，編碼的ha - axud1融合蛋白帶有流感病毒凝血素ha的表位標記肽段。
  18. There are four main parts in the paper, i. e. first of all, the dissertation studies the steady - state performance of repmsm with the theory of vector graph and equivalent electro circuit. characteristic of power angle, determinant of static of motor moving, losses and armature reaction are analyzed in this part

    論文研究稀土永磁同步電動機的穩態性能，結合向量圖和等值電路理論對稀土永磁同步電動機穩定運行進行了深入細致的分析，包括功角特性，電機運行狀態的判定，損耗和電樞反應等稀土永磁同步電動機自身具有的特點。
  19. Non - linear and non - equilibrium oscillatory behaviors are very common in biological systems, i. e. peroxidase - oxidase reaction, mitochondrion and cell systems

    一切生物體系本身均存在固有的非線性、非平衡振蕩行為。
  20. Thus, it becomes an importam issue to observe, measul ' e and analyze the biological reactions within the living organism as transient and dynamic reaction

    由於細胞內分子間的相互作用是一個動態平衡過程，因此實時分析生物分子間短暫的動態過程是必要的。
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