表面激活 的英文怎麼說

中文拼音 [biǎomiànhuó]
表面激活 英文
surface activation
  • : Ⅰ名詞1 (外面;外表) outside; surface; external 2 (中表親戚) the relationship between the child...
  • : Ⅰ名詞1 (頭的前部; 臉) face 2 (物體的表面) surface; top 3 (外露的一層或正面) outside; the ri...
  • : Ⅰ動詞1 (水因受到阻礙或震蕩而向上涌) swash; surge; dash 2 (冷水突然刺激身體使得病) fall ill fr...
  • : Ⅰ動詞1 (生存; 有生命) live 2 [書面語](救活) save (the life of a person):活人無算 (of a goo...
  • 表面 : surface; superficies; boundary; face; rind; sheet; skin; outside; appearance
  • 激活 : activation; sensitization; activate; sensitize; active激活材料 active material; 激活劑 activating...
  1. Comprehensive cellular responses was found in human amnion fl cells following exposure to low concentration of mnng, such as the lowering of dna replication fidelity resulted from alteration of dna polymerase profile ; activation of a lot of transcription factors, such as api, creb, nf - kb etc ; clustering of egfr ( epidermal growth factor receptor ) and tnfr ( tumor necrosis factor receptor ) and activation of camp - pka - creb and jnk / sapk signal pathways

    我們發現,低劑量mnng處理后的人羊膜fl細胞有廣泛的細胞反應,並有多個信號轉導通路的和基因達的改變。例如dna復制保真度下降, dna聚合酶譜發生改變,應用報告基因技術和底物磷酸化檢出技術證明細胞一系列轉錄因子如ap1 、 creb 、 nf b等被,細胞受體如皮生長因子受體、腫瘤壞死因子受體發生聚簇,細胞信號轉導通路camp - pka - creb和jnk sapk被
  2. For example, we have found the clustering of egfr ( epidermic growth factor receptor ) and tnfr ( tumor necrosis factor receptor ) and the activation of camp - pka - creb and jnk / sapk pathways after mnng treatment

    例如細胞受體如皮生長因子受體、腫瘤壞死因子受體發生聚簇,細胞信號轉導通路camp kacgyb和jnk sapk被
  3. Activation of the complement may lead to killing of the microorganisms by direct lysis effect of complement system or the phagocytosis by the enhancement of the attachment of microbes to the phagocyte ( opsonization ). low serun concentrations of mbl in man is the basis for a common opsonic defect associated with recurrent infection

    它可選擇性識別多種病原體的糖結構,以不依賴抗體和c1q的方式補體,發揮溶破和間接調理功能,還能與吞噬細胞膠凝素受體結合而起直接調理作用。
  4. It is necessary to control the mechanical stimuli precisely in the studies of cardiac mechano - electrical feedback ( mef ). in the present study a ventricular pressure - clamping system has been developed, which can be applied to isolated - perfused rabbit hearts. controlled by a computer, this system not only can make the left ventricle follow a command defining the same pressure wave as that during a beating cycle under physiological condition, but also deliver mechanical stimuli with a proper waveform to the ventricle at a particular time phase. this system integrates multiple functions, including perfusing, pacing, recording of electrocardiogram and monophasic action potentials, and clamping and measuring of ventricular pressures in isolated - perfused hearts. thus, it is a distinct system for investigating the phenomena and mechanisms of cardiac mef at organ level

    在心臟機械電反饋的研究中準確控制機械刺是非常重要的.本研究室構建了一套適用於離體家兔心臟的心室壓力鉗系統.該系統通過計算機控制壓力鉗,不僅能模擬正常生理條件下左心室的壓力波形,還能在心室動周期的特定時相、以適當波形對心室施加機械刺.該系統集心臟灌流與起搏、心電圖記錄、單相動作電位記錄、心室壓力鉗制與測定等多種功能於一體,特別適用於器官水平上觀察機械電反饋現象並探討其機制
  5. Abstract : it is necessary to control the mechanical stimuli precisely in the studies of cardiac mechano - electrical feedback ( mef ). in the present study a ventricular pressure - clamping system has been developed, which can be applied to isolated - perfused rabbit hearts. controlled by a computer, this system not only can make the left ventricle follow a command defining the same pressure wave as that during a beating cycle under physiological condition, but also deliver mechanical stimuli with a proper waveform to the ventricle at a particular time phase. this system integrates multiple functions, including perfusing, pacing, recording of electrocardiogram and monophasic action potentials, and clamping and measuring of ventricular pressures in isolated - perfused hearts. thus, it is a distinct system for investigating the phenomena and mechanisms of cardiac mef at organ level

    文摘:在心臟機械電反饋的研究中準確控制機械刺是非常重要的.本研究室構建了一套適用於離體家兔心臟的心室壓力鉗系統.該系統通過計算機控制壓力鉗,不僅能模擬正常生理條件下左心室的壓力波形,還能在心室動周期的特定時相、以適當波形對心室施加機械刺.該系統集心臟灌流與起搏、心電圖記錄、單相動作電位記錄、心室壓力鉗制與測定等多種功能於一體,特別適用於器官水平上觀察機械電反饋現象並探討其機制
  6. The effort of manganese removal was studied and the kinetics of manganese removal was tried to establish. the factors of dissolved oxygen concentration, fe2 + concentration, ph, p concentration and closing of the filter were studied to evaluate their effort for biological manganese removal, and the correlation of residual manganese and oxidation - reduction potential was also discussed. as the iron content of water was high, experiment results showed that the reaction was zero order, as the iron content of water was low, the reaction was first order. the time needed for the cultivation of biological manganese removal was 60 70 days. the filter operated at the filtration rate of 8 10m / h, silica sand of effective size 0. 95 1. 25mm filled the filter to a depth of 1200mm

    試驗結果明,成熟后濾砂濾膜的x射線衍射圖譜與mno _ x ? 5h _ 2o ( x = 1 . 86 )的x射線衍射圖譜一樣,濾膜成熟后的結構在進水物質不發生變化的情況下不發生變化;合適的碳磷比對生物除錳有明顯的促進作用,試驗條件下的投磷量不會對出水造成二次污染;生物除錳需要亞鐵的參與,亞鐵的存在除了能夠促進微生物分泌胞外酶並刺性外,還通過鐵離子的變價傳遞電子,催化錳離子的氧化反應,從而促進對二價錳的降解。
  7. The use of the state - of - the - art laser facility makes it possible to create conditions of the same or similar to those in the astrophysical processes. the introduction of the astrophysics - relevant ideas in laser - plasma experiments is propitio us to the understanding of the astrophysical phenomena. however, the great difference between the laser - produced plasmas and the astrophysical processes makes it awkward to model the latter by laser - plasma experiments. this paper addresses the physical backgrounds for modeling the astrophysical plasmas by laser plasmas, connecting these two kinds of plasmas by scaling laws. thus, allowing the creation of experimental test beds where observations and models can be quantitatively compared with laser - plasma data. special attentions are paid on the possibilities of using home - made laser facilities to model astrophysical phenomena

    採用當前最先進的光裝置與物質相互作用,可以獲得與天體物理過程中相同或相似的條件,並進而開展利用光等離子體模擬天體物理現象的實驗.然而,光等離子體為微米空間尺度、納秒存時間,而天體物理對象則為宇宙學的極大的時間與空間尺度,對在物理上和實際操作上將這兩種上存在巨大差異的物理過程對應起來從而利用光等離子體研究天體物理過程的可能性進行了討論,特別是對利用國內的光裝置開展模擬實驗的可行性進行了討論
  8. A reliability experiment of thermal aging was carried out for the two types of joints, scanning electron microscopy, energy dispersive x - ray spectrometer and micro x - ray diffractomer were adopted to investigate the interfacial evolution behavior of joints, and kinetics model of imc formation was established. the results show that imc growth follows the parabolic law as a function of aging time at certain aging temperature, imc growth is more sensitive to the aging temperature than the aging time, the activation energy of cu - al imc growth is 97. 1kj / mol and the major forming cu - al imc are cual2 and cu9al4, the activation energy of au - al imc growth is 40. 1kj / mol and the main au - al imc are au4al and au5al2, with au2al and aual at the interfacial periphery of joints, the rate of cu - al imc growth is about 1000 times slower than that of au - al imc, and kirkendall voids and cracks are easily appeared during thermal aging in gold ball bonds while voids and cracks are absent in copper ball bonds even after aging at 200 for 2900 hours and 250 for 169 hours

    研究結果明:金屬間化合物厚度與老化時間的關系符合拋物線法則,金屬間化合物的生長對老化溫度比老化時間更加敏感; cu - al金屬間化合物生長的能為97 . 1kj / mol ,老化后金屬間化合物呈層狀分佈,主要相為cual2和cu9al4 ; au - al金屬間化合物生長的能為40 . 1kj / mol ,主要相為au4al和au5al2 ,同時在界周邊區域生成了au2al和aual ;老化過程中cu - al金屬間化合物生長速率比au - al金屬間化合物生長速率小103數量級;金絲球鍵合點200老化96小時出現了明顯的kirkendall空洞和裂紋,但銅絲球鍵合點200老化2900小時和250老化169小時都沒有形成空洞和裂紋。
  9. Elevation of intracellular calcium ions may be partly induced by increased influx through sarcolemma l type - calcium channels. intracellular calcium elevation, on one hand, would activate calpain, a calcium - dependent cysteine protease that degrade the myofibrillar proteins and cause muscle atrophy ; on the other hand, result in activation of calcineurin which enhance the activity of mhc i promoter and inhibit a shift of mhc isoforms from slow to fast in soleus

    這樣,可能使得萎縮比目魚肌細胞內鈣離子水平升高,細胞內鈣離子靜息濃度的增加一方calpain ,增加收縮蛋白的降解,使肌肉萎縮;草四軍醫大月卜祠成士學位論文另一方通過鈣調神經磷酸酶,增加快型mhc基因的達,使骨骼肌肌球蛋白重鏈( mhc )發生由慢型向快型的轉化。
  10. Predicted tertiary structure showed that thl2 protein possessed a domain, and the srk - binding site cppc is located in tertiary structure surface, which provided the spacial foundation for thl2 binding srk kinase

    預測的thl2蛋白質高級結構中有一個結構,並且其與srk結合的性位點cppc位於蛋白質的,這為thl2蛋白與srk酶結合提供了空間上的基礎。
  11. This response was mediated by gi and subsequent activation of phospholipase c ( plc ), which triggered two pathways : protein kinase c ( pkc ) led to repulsion, and inositol 1, 4, 5 - triphosphate ( ip3 ) receptor activation led to attractive turning

    信號轉導機制的研究明, sdf - 1和baclofen了生長錐的g蛋白耦聯受體,通過gi將信號傳遞給plc ,進而pkc和ip3信號通路。
  12. The characteristics of this method are : a, directly counting cell number without the influence of the metabolic state of the cells ; b, discrimination of target cells from effector cells in cell - mediated cytotoxicity assay ; c, less treatment step, and free - radioactivity ; d, high sensitivity and reliability. 2, using the above assay, immunofluorescent labeled technique, and flow cytometry, the pbmc proliferation, apoptosis, necrosis, cell cycle, activation, cytokines and membrane marker were detected. the results showed that the number of pbmc reduced, but the activity of pbmc increased dose - dependently ; the reduction of cell number resulted from necrosis and apoptosis ; the supernatant of k562 cell lines were not able to block the cell cycle, but to promote it ; the ratio of t cell subset and the expression of thl and th2 cytokines increased

    結合以上創建的方法和免疫熒光流式細胞術,用k562細胞株可溶性分泌物(上清)對外周血單個核細胞( pbmc )進行培養以模擬體內微環境,然後分別從細胞增殖、凋亡、壞死、細胞周期、性、細胞因子和抗原達等方進行研究,結果發現用腫瘤上清培養的pbmc細胞數量下降明顯,但同時對其有作用,且呈劑量依賴性;細胞數的下降主要是由細胞壞死和凋亡引起的,腫瘤上清對細胞周期沒有阻斷作用,反而略有促進作用; t細胞亞群比例增加,並促進達th1 、 th2細胞因子。
  13. These quenching centers can quench both blue emission related to the surface defects and the orange emission of mn2 + impurities. they are most likely originated from the dangling bonds of the lone pairs on surface s2 " or the zn2 + vacancies

    這種猝滅中心對自藍光和橙光發射都有猝滅作用,它們極有可能來自s ~ ( 2 - )孤對電子的懸空鍵或zn ~ ( 2 + )空位。
  14. Dendritic cells ( dc ) is the most powerful apc, which can markedly increase the antigen - presentation capacity by maximizing the pepitide - mhc complexes on the cell surface and upregulating the co - stimulatory ligands b7 - 1 and b7 - 2, adhesion moleculees such as il - 12 that promote full activation of lymphocytes. full activation of antigen - specific t cells requires two signals - one signal coming via the tcr and the other signal through engagment of co - stimulatary molecules. t cells receiving one signal via their tcr are turned off by mhc ( major histocompatibility complex ), via t cell cd28 binding to b7 on the dc induce tlymphokine and t cell proliferatiion

    T細胞介導的細胞免疫在控制腫瘤生長方發揮著重要作用, t細胞在發揮抗瘤效應(分泌細胞因子和直接殺傷)之前必須先經過化,體內專職抗原提呈細胞( apc )細胞並使其化,樹突狀細胞( dendriticcell , dc )為t細胞的提供雙重信號, t細胞藉助tcr識別由dcmhc分子遞交的抗原肽后,通過tcr - cd3復合體傳遞抗原特異性識別信號(第一信號) ,以cd28為主的t細胞輔佐分子識別dcb7分子,傳遞非特異性協同刺信號(第二信號) ,在機體抗腫瘤免疫應答中處于核心地位。
  15. Abstract : plant responses to salt stress via a complex mechanism, including sensing and transducing the stress signal, activating the transcription factors and the corresponding metabolizing genes. since the whole mechanism is still unclear, this review emphasize the biochemical events during the plant adaptation to salt stress referring to an index of importance : the homeostasis in cytoplasm, the biosynthesis of osmolytes and the transport of water. most of these biochemical events were elucidated by study of halophyte and salt - sensitive mutations, also many important genes involved were cloned and used to generate stress - tolerance phenotypes in transgenic plants. on the other hand, about the molecular mechanism in signal transduction, the research of arabidopsis mutations and yeast functional complementation provided helpful traces but not full pathway

    摘要植物對鹽脅迫的耐受反應是個復雜的過程,在分子水平上它包括對外界鹽信號的感應和傳遞,特異轉錄因子的和下游控制生理生化應答的效應基因的達.在生化應答中,本文著重討論負責維持和重建離子平衡的膜轉運蛋白、滲調劑的生物合成和功能及水分控制.這些生理生化應答最終使得液泡中離子濃度升高和滲調劑在胞質中積累.近年來,通過對各種鹽生植物或鹽敏感突變株的研究,闡明了許多鹽應答的離子轉運途徑、水通道和物種特異的滲調劑代謝途徑,克隆了其相關基因並能在轉基因淡水植物中產生耐鹽型;另一方,在擬南芥突變體及利用酵母鹽敏感突變株功能互補篩選得到一些編碼信號傳遞蛋白的基因,這些都有助於闡明植物鹽脅迫應答的分子機制。
  16. Abstract : based on the concept of space migration length of photo - activation species, the analytical expression of the total number n of photo - activation species that can reach a segment on the substrate in the cubic deposition reaction space is derived. the simulation of the relationship of deposition rate and position of substrate is also completed. the simulation result agrees with the experiment data well

    文摘:基於光物質空間遷移長度的概念,推導出方形反應空間中到達基片上單位積的光物質總數的解析達式,對光化學汽相沉積中淀積速率和基片位置的關系進行了模擬和分析.模擬結果同實驗結果符合良好
  17. On a different dimension, the apparent inequality or exploitation has also led to increasingly militant or even terrorist action by interest groups of one type or another, and before anybody gives it any serious thought we have the globalisation of terrorism

    另一方的不平等或剝削也會促使一些利益集團採取愈來愈烈的行動,甚至從事恐怖動。結果大家未及細想這方的問題,恐怖主義動已經邁向全球化。
  18. Effective activation of antigen - specific t cells not only requires the first signal transduction through t - cell receptor ( tcr ) binding with peptide - mhc complex on the antigen presenting cell ( apc ), but also needs the second signal, termed costimulation. costimulation critical to the degree and consequence of t cell activation is provided by interaction between soluble factors or cell - surface molecules on the t cell and on the apc

    而t細胞的化除需要t細胞受體( tcr )與抗原呈遞細胞( antigenpresentingcell , apc )的抗原肽- mhc復合物結合所形成的第一信號外,還需要t細胞和apc的其它膜分子結合所提供的共刺信號(亦稱第二信號或輔助刺信號, costimulatorysignal )的參與。
  19. On one hand, these organic function groups decorate the surface of nanoparticles by combining with the surface dangling bonds. and most important, they may act partially as the donor of d - a pairs in the sa luminescence by providing electrons

    討論了吸附在納米顆粒的一oh ,一ch = ;和一coo等有機官能團的作用,明確提出了這些官能團中的一部分可能充當了自發光施主一受主對中施主的觀點
  20. The first part, flow cytometry assay research for molecules in the surface of platelets section l flow cytometry methodology research for detecting cd62p reserve of preserved platelets stimulated with thrombin objective 1 ) to establish and optimize a flow cytometry method which is used to test cd62p reserve incubated with thrombin ; 2 ) daily determinating the cd62p reserve of platelets stored at 22 ? to assess its value in evaluation of preserved platelet quality

    研究主要分為四部分:第一部分,血小板膜分子流式細胞術分析新方法和指標的建立第一節,流式細胞術測定保存血小板再達cd62p方法的建立目的1建立並優化測定血小板再達膜表面激活標志物cd62p能力的流式細胞術( fcm )方法。
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