移載后 的英文怎麼說

中文拼音 [yízǎihòu]
移載后 英文
postplanting
  • 移 : Ⅰ動詞1. （移動） move; remove; shift 2. （改變; 變動） change; alter Ⅱ名詞（姓氏） a surname
  • 載 : 載Ⅰ名詞（年） year : 一年半載 six to twelve months; six months to a year; 三年五載 three to five ...
  1. Fist of all, on the basis of the research of agone boffins, this author investigates the interaction mechanism of bolts and rock, and introduces the elastic ? lastic analytical resolution which is consist of the liner structure, the equivalent reinforced wall rock and the original wall rock in the simple loading from the equivalent well - proportioned view ; this solution is very important meaning for the engineering design. on the basis of coulomb friction model, the author introduces the finite element equation of the contact problem in order to provide the academic foundation for the application of msc. marc. finally, combining the engineering practice of the non - linear analysis of shield tunnel through yellow river of the south - north water transfer and using the model of friction, the author researched the evolution law of stress and displacement field in the structure of grouted rock bolts, and analyzed the effect to the stress and deformation of surrounding rock mass due to anchor supports

    首先，在前人研究成果的基礎上，對錨桿與圍巖的相互作用機理進行研究，利用全長錨固錨桿的中性點理論，從等效均化的角度來考慮錨桿對圍巖的加固作用，並推導了在簡單荷載作用下，含有襯砌、等效加固后的圍巖、原始圍巖三者的彈塑性解析解，對工程設計有著重要的參考意義；在數值模擬方面，以考慮錨固圍巖滿足規則化庫侖摩擦模型為基礎，利用虛功原理推導了接觸問題的有限元方程的計算格式，為開發運用大型商用有限元軟體msc . marc提供了理論根據，也形成了本文的理論基礎：最後，論文以南水北調東線穿黃隧洞穩定性分析項目為工程實例，利用本文所述的接觸問題的摩擦模型理論，對錨桿支護結構的應力場、位移場的變化規律進行了研究，分析了加錨支護對隧洞圍巖應力、變形的影響。
  2. Application of real - time quantitative pcr for guidance therapy of cytomegalovirus infection after allo - hematopoietic stem cell transplantation

    造血幹細胞移植后對人巨細胞病毒感染病毒載量的檢測
  3. As for the devitalized grafts, although the clinical results were various, some researchers regarded them as a biologic bandage at best, namely, the devitalized grafts lacked the capability of dominating the specificity of the overlying epithelium

    至於去活性的移植體，文獻記載中，臨床結果雖然不盡相同，好些研究者認為它們充其量只不過是生物性繃帶，並沒有能力決定自身在愈合后的組織種類（例如角化或非角化） 。
  4. The animal experiment is carried out in the first hospital of shanghai through renovating the injured nerve of the rats. four projects are used in this experiment : the conduits coated with pgla, the conduits coated with chitosan, the conduits coated with chitosan adding bridge - yarn and self - nerve migration. after 12 weeks, we observe and analyze the thickness of marrow theca, the diameter of axone, the density of regeneration nerve and then do electromyography and statistics analyzing, finding out that the third conduits have the best recovering effects on the injured nerve, close to the self - nerve migration

    因此我們選用加筋結構神經導管進行動物實驗。本課題動物實驗在上海市第一人民醫院進行，分別通過加筋結構塗pgla導管、加筋結構塗甲殼胺導管、加筋結構塗甲殼胺並加載縫芯線導管和自體神經移植四種方案對大鼠進行損傷神經修復實驗。在術后12周對四種方案再生神經的髓鞘厚度、軸突直徑、數量密度進行觀察分析，並進行肌電圖檢測和統計學分析。
  5. 1 m 0. 5, the phase - shifted angle 6 is controlled in term of sine law which makes the magnitude of resonant voltage track a reference sine voltage, and the resonant voltage is rectified, filtered, inverted and then the better sine - voltage output is obtained, theoretical analysis and experimental results show that for the resistive load and inductive load, the switches of leading leg of the phase - shift - controlled circuit are always turned on at zvs, and ones of lagging leg are turned on at zvs ( < 0 ) or turned off at zcs ( ( > 0 ), moreover, all switches in the low - frequency inverter are always turned on and off at zvs, the measured circuit efficiency for rated load reaches up to 88 %

    從功率單向流動角度出發，提出了一種lcc諧振型恆頻移相單相高頻鏈逆變電路拓撲，在調制系數0 . 1 m 0 . 5情況下，控制移相角按正弦規律變化，使諧振電壓脈沖列的幅值追蹤參考正弦電壓信號，經過整流、濾波、低頻逆變，從而獲得正弦度較好的輸出電壓。理論分析和實驗結果證明對于阻性負載或阻感性負載，移相全橋具有超前橋臂零電壓開通，滯后橋臂或者零電壓開通（ _ 0 ）或者零電流關斷（ _ 0 ）的軟開關特性，而低頻逆變器的各個開關均實現零電壓條件下的開通與關斷。
  6. And do any custom data migration work in your own after the update is finished

    下載更新，並在完成更新后自己執行任何自定義數據遷移工作。
  7. For meeting the related nantional standards and avoiding demolishment of the building, the underpinning and strengthening methods are used, with which the loads of center column are underpined by the diagonal steel strut and the cross - sectional areas of side pillar are strengthened, both ends of shear wall are chiseled in turn and then concrete is poured again

    通過採用斜向鋼支撐荷載轉移法實現對中柱的托換，採用剪力墻兩端分批鑿除后再澆搗實現對剪力墻的托換，採用增加截面法對邊柱進行加固，使建築物經托換和加固后能滿足國家有關規范的要求。
  8. An infectious eiav clone was recovered by transfecting fatal donkey dermal ( fdd ) cell cultures and donkey leukocyte ( dl ) culture in vitro with the full - length gene clone of dv. the virus ( designed pd70344v ) derived from the third passage in dl culture was observed by electron microscope and the reverse transcriptase ( rt ) activity was determined

    將包含全基因片段的三個基因克隆以限制性內切酶消化后順次連接克隆到載體ptz18r上，構建了4個全長基因的分子克隆，分別命名為pd30343 、 pd70333 、 pd70343 、 pd70344 ，其中兩個轉移到低拷貝載體plg338上，命名為plgd30343 、 plgd70344 。
  9. The improvement system is made up of the pressure sensor, flow sensor, displacement sensor, electro - hydraulic proportional flow control valve, power amplifier, data gathering board and computer. the platform can carry out testing the hydraulic parameters, processing the tested data, saving the processed data and drawing, adjusting the pressure automatically

    改造后的測控系統主要由壓力傳感器、流量傳感器、位移傳感器、比例節流閥、功率放大器、數據採集卡和計算機組成。改造后的實驗臺具有自動採集實驗數據、自動處理實驗數據、自動保存實驗數據、自動調節液壓系統負載壓力等功能，大大提高了實驗臺的工作效率、測試精度和智能化水平。
  10. We represent a temperature model of surface carrier mobility of short channel most after thinking about kinds of dispersion effect

    在考慮了各種散射效應對遷移率的影響后，提出了短溝道most表面載流子遷移率的溫度模型。
  11. R the theoretical analysis ignored the distortion of the section and worked out the equations of displacement, loading capacity by means of energy method

    理論分析忽略變形后截面畸變，採用能量法，推導出檁條的位移、承載力的計算公式。
  12. After it starts, not only adds 35 % pressure to edge of shovel, also moves the part weight of front shaft of vehicle to the tail shaft, which can improve 25 % frictional resistance

    系統啟動后，不但能對雪板的鏟刃增加35 %的壓力，而且還會把車輛前軸的部分載荷轉移至后軸，這樣可提高25 %后輪對地面的摩擦力。
  13. It really provides convenience to evaluate and optimize the design result. 3 ) vibration analysis has been fulfilled by calling some math libraries and graphic libraries in matlab to plot graphics such as velocity - time, displacement - velocity, step response, impulse response, gain - frequency and phase - frequency. we can know the capabilities of the spring system from the graphics

    3 、在matlab環境下調用相應的數學函數庫和圖形庫對設計的彈簧進行分析，繪制彈簧加載后系統的速度-時間響應曲線、速度-位移響應曲線、階躍響應曲線、脈沖響應曲線、增益-頻率響應曲線和相角-頻率響應曲線，根據曲線來分析系統的各項性能。
  14. Because of continuity of load effects in time and space, displacement effects of previous time period in the latter time period and effects in various places have been taken into accounts. it is on these basis that the paper puts forward the dispersed counting way discrete algorithm based on such relationship, takes time - stepping integration to calculate rails " dynamic response, uses fortran language to write counting program, and conducts computer mock tests about rails " power response

    由於荷載作用在時間和空間上的連續性，因此考慮了前一時間段所產生的位移對后一時間段的影響以及不同位置的相互影響，在此基礎上提出了基於車輪、軌道、枕木相互關系的離散化演算法，採用時間步長積分計算了軌道的動力響應，使用fortran語言編制計算程序對軌道動力響應進行了模擬。
  15. In order to get the soluble recombinant eo protein and inspect the protein expression status convinently, the egfp and eo gene were ligated into baculovirus transfer vector. with the co - transfecting sf9 cells of baculovirus recombinant transfer vector and linearized viral dna, and plaque purification in the posttransfection procedure, the pure recombinant baculovirus were harvested, which infected the sf9 cells for amplifying to generate a p - l stock. in the meantime, the fluorescence microscopy detection indicated expressed egfp protein to confirm the heterogenous protein expression of recombinant baculovirus. the pi - stock from a pure plaque was used to generate a high liter p - 2 stock, which was determined in liter as 1. 14 107pfu / ml by performing a plaque assay. when a volume of p - 2 stock infected the sf9 cells with moi 5 - 10 for expression, the strong fluorescence was obeserved on the day 3 of postinfection

    此外，為了得到可溶性重組eo蛋白並便於觀察重組蛋白的表達情況，我們將egfp基因與eo基因相連插入昆蟲桿狀病毒轉移載體中，與線性桿狀病毒dna共轉染sf9細胞后通過噬斑純化得到純的重組桿狀病毒，將其感染sf9細胞制備p1種子液，同時用熒光顯微鏡觀察綠色熒光蛋白的表達情況剔除表達效果差的重組桿狀病毒。再用p1種子液感染sf9細胞制備高效價的p2種子液。通過病毒液的梯度稀釋和噬斑測定，確定p2種子液的病毒滴度達1 . 14 10 ~ 7pfu ml 。
  16. Hegf gene with his - tag at the end, which was derived from pet22 - egf, was in - frame fused to the carboxy - terminal of polyhedrin ( ph ) gene, which included the amino - terminal 116aa coding region. the polyhedrin - egf fusion gene ( named ph - egf ) was then cut out with ecorv and ecori, and was cloned between ecorv and ecori sites of pbacpak. 8 ( the result plasmid was named pbacph - egf and the ph - egf fusing gene was right under the control of ph promoter ). the pbacph - egf structure was verified with restriction enzymes digestion and pcr

    從pet22 - egf質粒中分離出末端帶his - tag的egf基因，對位融合於多角體蛋白n端116個氨基酸基因序列的下游（命名為ph - egf ） ，並在兩段基因間設計了凝血酶xa蛋白酶切位點，經過酶切、測序等鑒定正確后，克隆至pbacpak8中，使ph - egf融合基因置於多角體蛋白（ polyhedrin ， ph ）基因啟動子控制之下，構建成重組轉移載體pbacph - egf 。
  17. The recombinant pcr technic was used to introduce a linking peptide klgggg to the site between scfv single chain form of the monoclonal antibody sz - 51 specific for the glycoprotein gmp140 on activated platelet membrane and uk32 low molecular weight form of pro - urokinase, to make the scfv - linker - uk32 chimeric gene. this gene was cloned into the transfer vector pbacpak9, and cotransfected with bacpak6 bsu36i digest into sf 9 cells. the fusion protein was secreted into the medium. in the fifth day after the cotransfection, the supernatant of the medium showed 107 iu ml fibrinolytic activity, higher than 25 iu ml fibrinolytic activity of scfv - uk32. elisa showed that the supernatant had the binding activity to activated platelet. wastern blotting also indicated that the supernatant could bind to the monoclonal antibody of urokinase b chain

    為了提高重組導向溶栓分子scfv - uk32的溶纖活性，通過重組pcr方法在編碼scfv與uk32的堿基之間引入編碼klgggg連接肽的堿基序列，並克隆到轉移載體pbacpak9上，通過與線性病毒dna bacpak6 bsu36i digest共轉染到昆蟲細胞sf 9內，進行表達。表達產物分泌到上清中，共轉染后第5d天用纖維平板法測得sf 9細胞上清溶纖活性達到107 iu ml ，比未引入連接肽的scfv - uk32的表達活性25 iu ml高。
  18. Then bm cell line was co - transfected with parental bm - npv dna and the transfer plasmid pvl - nk, the recombinant virus was then obtained subsequently with routine procedure. nattokinase was expressed in silkworm larva by injection with the recombinant virus

    將nk基因克隆至轉移載體pvl - 1393中後用常規方法獲得重組病毒，感染家蠶后納豆激酶獲得正確表達。
  19. And then a 378bp acci fragment in pbtk2. 6 was replaced by a fragment containing the immediate early promoter of cytomegalovirus and bovine growth hormone polyadenylation signal derived from pcr3 - uni, a eukaryotic expression plasmid

    在此基礎上，進一步用tthlll酶切后，補平插入帶有sv40啟動子的大腸桿菌?半乳糖苷酶報一告基因（ lacz ） ，獲得通用轉移載體pltk - uni 。
  20. Fusion gene by pcr was inserted into bombyx mori baculovirus transfer vector pbacpak. 8 and contransfected with lineared dna of bm - bacpak6 virus into bmn cells. the homologous recombination occurred inside the cells, and the recombinant virus bacpak - 6aa - hgm - csf was expressed, as identified by pcr and southern hybridization. the bmn cells and the fifth instars were infected by the recombinant virus bacpak - 6aa - hgm - csf

    本研究首先通過pcr將家蠶桿狀病毒多角體蛋白起始密碼子后的18個堿基引入到hgm - csf基因的5 』端之前，然後將融合基因重組與家蠶桿狀病毒轉移載體pbacpak8中，獲得重組轉移載體pbacpak8 - 6aa - hgm - csf ，並與線性化bm - bacpak6dna共轉染家蠶細胞株，獲得重組病毒bacpak - 6aa - hgm - csf 。
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