誘導表示 的英文怎麼說

中文拼音 [yòudǎobiǎoshì]
誘導表示 英文
induced representation
  • 誘 : 動詞1. （誘導） guide; lead; induce 2. （使用手段引人隨從自己的意願） lure; seduce; entice
  • 導 : 動詞1. （引導） lead; guide 2. （傳導） transmit; conduct 3. （開導） instruct; teach; give guidance to
  • 表 : Ⅰ名詞1 （外面;外表） outside; surface; external 2 （中表親戚） the relationship between the child...
  • 示 : Ⅰ動詞（擺出或指出使人知道; 表明） show; indicate; signify; instruct; notify Ⅱ名詞1 [書面語] （給...
  • 誘導 : guide; lead; induce; guidance; induction
  • 表示 : show; express; mean; indicate; expression; presentation; signifying; remark; representation
  1. At the same time, differen t arrays of electrodes have been studied. flow visualization has shown that the plasma between symmetric streamwise electrode strips ca n ' t induce flow velocity at the same phrase driving but can at multi - phrase driving, and asymmetric streamwise eledtrode strips can induce flow velocity both at the same phrase and at multi - phrase driving in still air. in principle, the experimental results correspond to that of the cooperant research between university of tennessee and nasa langley research center

    流動顯示實驗表明，在一個大氣壓下，對于電極對稱分佈的情況，在同相位的射頻激勵下，靜止的空氣中沒有明顯的現象，而在多相位射頻激勵下，靜止空氣中的二維平板上可以產生推力，誘導了流場；對于電極的非對稱分佈的情況，在同相位或多相位的射頻激勵下，都能在二維平板上產生推力，並誘導流場。
  2. We showed here that axudl mrna expression was elevated by tgf - 1 treatment in a time and dose - dependent manner in hepg2 hepatoma cells and spc - a1 lung carcinomas cells, and also indicated that de novo protein synthesis was required for this response using the protein synthesis inhibitor cycloheximide, suggesting that axudl is a primary target of tgf - signalling

    在hepg2和spc - a1細胞中， tgf - 1能明顯誘導這兩種細胞中的axud1基因的表達，而且表現出時間和濃度的依賴效應。同時，利用第一軍醫大學博士學位論文蛋白質合成的特異抑制劑還發現， tgf一pl誘導的axudl基因的表達過程需要新的蛋白質的合成，提示axudl基因是tgf一p信號通路的一個主要靶分子。
  3. In this paper we have done two work, one is we, in the dressed states representation, reveal that the constructive interference of atomic coherence on absorption leads to electromagnetically induced absorption, which is in sharp contrast to the case in which destructive interference of atomic coherence gives rise to electromagnetically induced transparency and the other is we reveal that coupling field linewidth inhibits electromagnetically induced absorption, by employing a four - level system in which three transitions are in n configuration and the middle transition serves as a probe transition

    本文主要做了兩方面的工作：一是在修飾態表象中揭示修飾態原子相干對吸收的相長干涉產生電磁誘導吸收，這與修飾態原子相干對吸收的相消干涉導致電磁誘導透明的情形形成鮮明的對照。二是在裸態中，引入耦合場的線寬，從而發現耦合場的線寬抑制電磁誘導吸收。首先研究電磁誘導吸收。
  4. In addition, axud1 has a high homologue with transforming growth facotr beta ( tgf - ) induced apoptosis protein 2 and 12 using blast exploration at genebank database. these suggest that axudl may have a tumor - suppressor function in these organs and may play an important role in tgf - - induced apoptosis

    通過genkbank上blast的搜索結果表明， axud1與tgf -誘導的凋亡蛋白2 、 12 （ taip - 2 、 taip - 12有較高的同源性，提示axud1可能是一個具有腫瘤抑制功能的基因，並可能在tgf -誘導的細胞凋亡中起著重要作用。
  5. The bell - shaped time course of the information entropy indicates that a forward mutation of " - resistant " hosts takes place, since no loss of cellular viability occurs for the second growth phase of reinduced ( i. e. recovered ) cells

    從誘導過程之鐘形訊息亂度之時間趨勢表示正向反應變異為-阻抗能力之宿主菌確實已發生，因為再誘導菌相細胞之第二生長期並未發生因感染而失去細胞存活之現象。
  6. Sds - page results showed that there was a clear target protein band in mut + recombinant supernatant after 48 hours of culturing, while a faint band only in muts recombinant after 72 hours. western - blotting result showed that there was no remarkable difference of yield between mut + and muts recombinants after 6 days induced. anti - virus activity tests revealed that culture supernatants of mut + and muts recombinants could inhibit tmv infection with high efficiency in the same concentration and there was no significant difference between them

    結果表明，誘導培養48小時后， mut ~ +重組菌株表達產物在sds - page膠上顯現出清晰的目的蛋白帶，而mut ~ s重組菌株培養72小時才能顯示微弱的目的帶； western - blotting雜交信號強度表明，同樣培養6天的mut ~ +和mut ~ s重組菌株表達產物在表達量上沒有明顯差別。
  7. The flow visualization indicates the primary cause of the phenomena to be a combination of mass transport and vortical structures induced by strong paraelectric and peristaltic electrohydrodynamic ( ehd ) body forces on the flow. the main jobs of this paper can be generalized as follow : 1

    流動顯示結果表明了該實驗現象的初步原因，由於在自洽電磁場中等離子體的電流體（ ehd ）順電力與蠕動力誘導了渦和能量輸運所致。
  8. Finally, the atomic coherent population trapping is studied in a multilevel laser - induced continuum structure system including cascade two - photon processes by means of quasi - classical theory. the condition leading to the atomic coherent population trapping and the dark state are given explicitly. the effects of atomic initial state and the laser intensity on the populations distributed in the atomic bound states are discussed

    我們還運用準經典理論研究了含級聯雙光子過程的多束縛態激光場誘導原子連續態結構系統中原子布居數的相干俘獲，給出了產生相干俘獲的條件及暗態的表達式，討論了原子初態和激光強度對原於布居數的影響，揭示了原子相干對穩定rydberg原子的重要作用。
  9. Northern blot analysis showed that the mrna level of p27 k ' pl had no changes during ir responses ; the level of ubiquitinated p27klpl increased following 10gy - irradiation ; mg - 132 ( proteasome inhibitor ) inhibited the degradation of

    我們通過初步的研究結果揭示: northem檢測結果表明ir對p27kip 『 mrna水平無明顯影響; ir誘導p27kip 』泛素化水平的增加;蛋白酶體抑制劑（ mg一1
  10. Obvious increases in asa, gsh and sucrose content during dehydration and steep declines in subsequent rehydration indicated that asa, as well as gsh and sucrose, might be involved in protection of dehydrated boea leaves, but not for rehydrated ones

    利用mrna差異顯示技術分離到牛耳草葉片脫水過程中5個脫水敏感的cdna 、 52個脫水特異誘導表達的cdna 、 21個脫水上調的cdna 、 14個脫水下調的cdna 、 16個磷酸鹽處理誘導表達的cdna 。
  11. Then using ecbp21 antibody and immunogold transmission electron microscopy method, we studied the subcellular localization of ecbp21. the results indicated that the gold particles were mainly localized in the cell wall in callus cells and rachis cells of angelica dahurica. these results indicated that ecbp21 mainly localized in cell wall, which provide a direct evidence of the extracellular existence of ecbp21. furthermore, using ecbp21 antibody and immunohistochemical method, we studied the organic specially distribution of ecbp21, the results indicated that ecbp21 distributed in all organize, but it distributed more in leave n flower rachis than in leafstalk and root

    首先，構建了ecbp21表達載體，誘導了重組蛋白的表達，並通過膠回收法獲得了大量純化重組ecbp21蛋白，制備了高效價、高特異性抗體；隨后，利用ecbp21抗體，結合免疫膠體金電鏡定位技術進行了ecbp21亞細胞定位研究，結果顯示：在白芷愈傷組織細胞和花序軸細胞中金顆粒主要分佈在細胞壁區域，而在細胞內未發現或僅有少量金顆粒分佈，表明ecbp21蛋白主要定位於細胞壁區域，這為細胞外cambp （ ecbp21 ）的胞外存在提供了直接證據：進一步，利用ecbp21抗體，通過免疫組織化學分析研究了ecbp21組織特異性分佈狀況，結果表明ecbp21在白芷各組織中均有分佈，但在葉、花、花序軸中分佈較多，而在葉柄、根中分佈較少。
  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. And flow velocity can be induced in still air. consequently a new method about active flow control is discovered. flow visualization has shown that plasma between symmetric streamwise electrode strips ca n ' t induce flow velocity at the same phrase driving but can at multi - phrase driving, and asymmetric streamwise eledtrode strips can induce flow velocity both at the same phrase and at multi - phrase driving in still air

    本文的主要工作表現在以下幾個方面：一、成功研製了高效、經濟、可控的輝光等離子體發生器，利用自行研製的等離子體發生器一個大氣壓下產生了均勻可控的輝光等離子體，並進行了流動顯示實驗，採用ehd技術在靜止的空氣中誘導了流場，開創了主動流動控制一條新思路。
  14. Restin was a novel gene isolated by our lab from differentiation tumor cell induced by all - trans retinoic acid in 1999, and its molecular functions were not well understood. it mainly expresses in terminally differentiated cells. by transfection of restin into tumor cell, the cells were arrested in g1 phase and the cell proliferation was inhibited

    Restin是1999年本室在研究全反式維甲酸誘導細胞分化時克隆得到的一個人類未知功能的新基因，該基因主要表達于終末分化細胞，穩定轉染該基因的細胞出現g1期阻滯，抑制細胞的增殖，提示restin與細胞周期的調控有關。
  15. Bsp ( boyine seminal plasma ) protein is the cardinal protein in bovine sperm, which can combine with choline or phosphycholine and then adhere to the surface of sperm to promote the sperm capacitation induced by heparin and high density lipoproteins ( hdl ). moreover, bsp protein can combine with heterogeneous collagen, fibrinogen, heparin, calmoduline, igf - ii and apoa - i. bsp can also inhibit the migration of cholesterol on the sperm membrane

    前言bsp （ bovineseminalplasma ）蛋白是牛精漿中的主要蛋白質， bsp蛋白可以與膽堿或磷脂膽堿結合，黏附於精子表面，可促進由肝素、 hdl等誘導的獲能過程，另外bsp蛋白與不同來源的膠原、纖維蛋白原、肝素、鈣調蛋白、 igf - 、 apoa -等結合， bsp蛋白還可抑制精子胞膜上的膽固醇遷移，這些都暗示了bsp蛋白在精子胞膜的脂類代謝及調節精子的獲能以及頂體反應方面發揮重要作用。
  16. It was recognized as a brain - gut peptide since the peptide and its receptor exist in the central nervous system. previously, we demonstrated that motilin and motilides activates cells in paraventricular nuclei ( pvn ) reflected by increased gastric motility and induction of the immediate early gene c - fos in conscious rat, which suggests central motilin participates in the regulation of gastric motility. it was reported in 2001 that ghrelin is an appetite - stimu latory signal from stomach with structural resemblance to motilin

    胃動素（ motilin ， mt ）是由小腸上段粘膜內分泌細胞合成並分泌的22個氨基酸組成的腦腸肽，調節消化間期胃運動， pvn內給予胃動素和胃動內酯（ motilides ）可增強清醒大鼠胃運動，中樞微量注射胃動素可誘導pvn中立即早期基因c - fos的表達，提示中樞胃動素參與胃運動的調控，人ghrelin和胃動素之間有36的相似性，而且二者的受體之間有50的相似性，因而有人稱ghrelin為「胃動素相關肽」 。
  17. This gene was inserted into expressing vector pgex - 4t - 1, which could express a gst fusion protein in e. coli. strain bl21 ( de3 ) by iptg inducing

    將己該基因構建到融合蛋白表達載體pgex - 4t - 1 ，通過iptg誘導，進行原核蛋白表達， sds - page電泳顯示，有約48kd融合蛋白表達。
  18. The homologious comparison proved the cloned gene had 96 % homology to the sequence of the omp gene, and the alignment of the amino acid sequence was 98 %. the recombinant plasmid was constructed with the target gene and the expressing vector pgex - 4t - l and then was transformed into e. coli bl21 ( de3 ) the fusion protein was expressed under the iptg inducing condition, and exhibited about 62kda in size, very close to the predicted molecular weight of gst - momp. furthermore, the fusion protein was specifically recognized by anti - serum which raised against the major outer membrane protein of ahl316

    Sds - page電泳分析顯示誘導表達的基因產物分子量約為62kda ，與預測的gst -外膜蛋白重組融合蛋白的分子量極為相似， western - blot進一步證實，表達產物能被嗜水氣單胞菌l316主要外膜蛋白特異性抗血清所識別，產生明顯的染色條帶，說明所表達的基因產物與天然的外膜蛋白抗原性一致。
  19. Constructed the fusion protein expression vector of echistatin, . and identify it by dna sequencing. the vector can express echistatin fusion protein at a high level, the fusion protein molecular weight is about 16000 da in sds - page analysis, and the fusion protein consists more than 30 % of total protein, the fusion protein has specific antigen - antibody reaction with rabbit anti - echistatin polyclonal antibody. the fusion protein include : hpk5. his + 6tag, and echistatin. echistatin can be released by cnbr cleavage

    構建了echistatin融合蛋白表達載體，經dna測序鑒定正確后，溫控誘導表達，獲得了高效表達，表達產物經505一隊ge分析，分子量為16000oa ，符合預計的融合蛋白分子量，表達產物. ll 』菌體總蛋白的30 %以上， westem一blotting結果顯示，該日的蛋白能夠和echistatin多克隆抗體發生特異性抗原抗體反應，表明我們成功構建了eohistatin的高效融合表達克隆。
  20. The positive transformants with the integrates mn - sod gene was identified by zeocin - resistance, pcr screening and expression in p. pastoris. the recombinant mn - sod protein was successfully expressed in pichia pastoris based on the evidences that a relative molecular weight about 23kd appeard in sds - page, the obvious activity of sod existed in native - page and enzymatic activity test, and mn - sod activity was specific base on the inhibition with the mixture of chloroform - enthanol ( 3 : 5 / v : v ) and potassium cyanide. two secreted plasmids ppiczaa - sodm18 and ppiczaa - sodc were constructed and after there linearization were transferred into chromosome of pichia pastoris gs115 by electroporation

    Pcr鑒定及mut表型分析進一步說明，目標基因已經重組到宿主菌基因組染色體上； 0 . 5甲醇誘導表達后， sds - page結果顯示，表達的蛋白相對分子量約為23kd ，活性電泳出現明顯活性條帶；酶活性測定顯示，重組菌株sod活性比對照提高5倍左右；氯仿-乙醇（ 3 : 5 v : v ）和kcn （ 5mmol l ）抑制反應進一步證明，所表達的sod為錳超氧化物歧化酶。
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