終止端 的英文怎麼說

中文拼音 [zhōngzhǐduān]
終止端 英文
clearing end
  • 終 : Ⅰ名詞1 （最後; 末了） end; ending; finish 2 （指人死） death; end 3 （姓氏） a surname Ⅱ形容詞（...
  • 止 : Ⅰ動詞1. （停止; 攔阻） stop; cut out 2. （截止） close; end Ⅱ副詞（僅; 只） only; just Ⅲ名詞（姓氏） a surname
  • 端 : Ⅰ名詞1 （東西的頭） end; extremity 2 （事情的開頭） beginning 3 （門類; 方面） item; point 4 （原...
  • 終止 : 1 （結束） stop; end; suspend 2 （停止） termination; annulment; abrogation 3 [音樂] cadence; 終...
  1. Atu - c adsl transceiver unit central

    非對稱數位用戶迴路局端終止單元
  2. Atu - r adsl transceiver unit remote

    非對稱數位用戶迴路遠端終止單元
  3. Methods and applications of inserting a stop codon into a cloned gene with pcr

    在已克隆基因末端添加終止密碼的方法與應用
  4. 7. at the first time, the reporter dye, fam was linked to the 5 " - end of the oligonucleotides of the probes, and the tamra was located at the 3 " - end as quencher dye. we use camv35s and fmv promoter, nos terminater, mark gene nptii, and aim gene pat, epsps and cryla ( b ) genes as target sequences, design pairs of sp

    7 、首次以fam熒光素標記探針5 』端作為發光基團，以tarma標記探針3 』端為淬滅基團，以camv35s 、 fmv啟動子、 nos終止子、標記基因nptll 、抗除草劑基因epsps 、 pat 、抗蟲基因cry1a ）為檢狽目標，設計、篩選出特異性引物和探針，優化實驗參數，建立了轉基因植物通用性熒光pcr定性檢測方法體系。
  5. J mol biol., 1992, 224 : 53 - 63. 26 abe h, aiba h. differential contributions of two elements of rho - independent terminator to transcription termination and mrna stabilization. biochimie, 1996, 78 : 1035 - 1042

    通過計算，我們預測到266個不依賴終止子，其中包括232個蛋白編碼基因， 12個trna基因和3個rrna基因，約17 %不依賴終止子位於操縱子的末端。
  6. Informs the client - side exception - handling component that all message queuing attempts to deliver the message to the server were rejected, and the message ended up on the client - side xact dead letter queue

    通知客戶端異常處理組件，消息隊列將消息發送至服務器的所有嘗試均被拒絕，消息終止於客戶端的xact死信隊列。
  7. The amplification system was optimized so that the pcr with different primers can be carried out under the same condition. the pcr products were sequenced using sanger ' s terminator and fluorescent label techniques. sequences were analyzed and compared base on sequencing analysis3. 4 and seq / ede software

    方法根據mtdna控制區及其周圍區域的序列，設計多對引物，探索優化擴增體系，使擴增條件能夠同時滿足多對引物的需要，用sanger末端終止法及熒光標記技術對樣本進行dna測序， sequencinganalysis3 . 4和seq ede軟體進行序列分析和比對。
  8. A high efficiency dual - band rf power amplifier has an output and / or input of a high frequency transistor well terminated at the second harmonic frequency for dual - band operation

    本發明乃一種高效率雙頻射頻功率放大器，提供高頻電晶體的輸出端與?或輸入端于雙頻操作中有良好的二階諧波終止。
  9. The high - enzyme activity has 2 base changes, resulting in long amino acid sequence with native amylase. this inducing method resolved the problem of non - effective induction as in base analogue induction. and the method we used provide a new measure for this kind of work

    高酶活編碼區位點突變導致c -端序列變化和終止子的后移本誘變方法克服了用堿基類似物在體內誘變由於核酸復制酶等的校正作用而造成誘變無效的難題，為基因的誘變找到了一條新途經。
  10. It was pointed out that the extreme thought and autocratic policy of qin dynasty not only terminated the cultural prosperous situation of contention and flourishing of numberous schools of thought since the spring and autumn period and the warring states period, but also accelerated the collapse of qin dynasty itself

    指出焚書坑儒事件反映了秦王朝極端的思想專制政策，不僅終止了春秋戰國以來的百家爭鳴的文化繁榮局面，也加速了秦王朝本身的瓦解。
  11. Assuming the loop is known to be only a single straight segment of 26awg cable, there is no additive loop or afe noise, and the remote - end is terminated by a high - impedance load for all frequencies, figure 5 shows the resulting selt performance

    假定已知環路只有一個單個的直段26awg電纜，沒有附加的環路或者afe噪聲，對所有的頻率遠端通過一個高祖抗負載終止，圖5給出了selt的性能結果。
  12. Harmonized blank detail specification for lead screw actuated non - wirewound preset potentiometers - square form, container sealed, actuating device insulated from resistive element, slipping clutch at each end of travel, rigid terminations - assessment level s

    導螺桿傳動非線繞預調電位器協調空白詳細規范.正方形的容器密閉的與電阻元件絕緣的驅動裝置每個行程終止的滑動離合器剛性終端.評定級別s
  13. Using an 8 - depth async fifo solves the synchronization and exchange of data be - tween different clock domains. the data transaction protocol comes from the most basic work way of uart. when the master clock is 16. 7mhz, the pcm side and adpcm side clocks both are 2. 38mhz, the results of simulation show that the latency from the start - bit of pcm data inputting uart receiver to the stop - bit of adpcm data outputted uart transmitter is 14. 3 us and the latency from the start - bit of adpcm data inputting uart receiver to the stop - bit of pcm data outputted uart transmitter is 14. 7 us

    在主時鐘為16 . 7mhz ， pcm數據端與adpcm數據端時鐘均為2 . 38mhz時，模擬結果表明從pcm的起始位輸入uart接收器到adpcm終止位輸出uart發送器的最大延遲為14 . 3 s ，從adpcm的起始位輸入uart的接收器到pcm終止位輸出uart發送器的最大延遲為14 . 7 s ，設計時盡可能的使編碼與解碼的時間相差不多，從結果看出基本達到這個要求。
  14. Conclusion we have constructed the expression plasmid pbv220 - hpf4 successfully. 3 ' - utr of h pf4 c dna was deleted and tag was mutated to taataa by pcr. after sds - page and densitometric scan analysis, the expression level of r hpf4 is 25 - 30 %

    結論本研究運用pcr定點突變技術，完全去除了hpf4cdna基因3 」端utrat富含區：改用大腸桿菌強串聯終止密碼子taaaataa ，成功構建高效表達克隆pbv220 rhpp4 。
  15. The sequence encodes an open reading frame of 518 amino acids. there is a transit peptide of 74 amino acids in the n terminal of the putative amino acids sequence coded by the cdna

    該序列長為1758hp ，起始密碼子位於84 86hp ，終止密碼子為1658 166fop ，開放閱讀框長為1557hp ，編碼58個氨基酸序列，其中n末端含有74個氨基酸的轉運肽。
  16. In this research two full - length cdnas have been cloned by a combination of rt - pcr and 3 " - is1 - race with synthesized degenerate primers from young leaves of vicia faba l., pichia methanolica high - level expression systems of the genes have been constructed, and the milligram expressed protein was purified using probond resin purification system, which may result in further identification of the function of the aba binding protein. the full - length cdna of abp370 fragment is 3449 bp long and has an open reading frame of 2304 bp encoding 768 amino acids with 876 bp long 5 ' - utr, 369 bp long 3 ' - utr and poly ( a ) tail. the full - length cdna of abp640 fragment is 1012 bp long and has an open reading frame of 780 bp encoding 260 amino acids with 88 bp long 5 ' - utr, 144 bp long 3 " - utr and poly ( a ) tail

    3 - 5 - race擴增片段序列分析結果表明， abp370擴增片段的全長cdna為3449核苷酸，其中5非翻譯區為876個核苷酸， 3非翻譯區為369個核苷酸並末端帶poly （ a ）尾巴，從起始密碼子atg至終止密碼子tga ，含有一個編碼768個氨基酸殘基的開放閱讀框架（ 2304bp ） ； abp640擴增片段的全長cdna為1012核苷酸，其中5非翻譯區為88個核苷酸， 3非翻譯區為144個核苷酸並末端帶poly （ a ）尾巴，從起始密碼子atg至終止密碼子taa ，含有一個編碼260個氨基酸殘基的開放閱讀框架（ 780bp ） 。
  17. ( 2 ) starting off with analyzing the forces affected on single dry solid granule on the roller screen, the relative slippage and slipping condition of granule at the tangential direction and axis direction of roller screen are discussed, and the average slipping conveyance velocity from feeding end to discharging end is given. the throwing conveyance of granule is discussed, the throwing coefficient of roller screen and its varying rule, and the concept of average throwing coefficient and its computing method are put forward, the starting condition and terminating condition for throwing motion of granule on the roller screen and the throwing conveyance velocity of granule are researched. the influence on throwing motion of granule by the rotating velocity of roller screen is discussed as well

    （ 2 ）從筒式篩網上單顆干固相顆粒的受力分析著手，討論了顆粒在筒式篩網面上的切向相對滑動和軸向相對滑動及滑動條件，並導出了顆粒從進料端向出料端滑動運移平均速度；討論了顆粒的拋擲運移，給出了筒式篩網上的拋擲指數及其變化規律，提出了筒式篩網的平均拋擲指數的概念及計算方法，研究了筒式篩網上顆粒拋擲運移的產生條件和終止條件，以及顆粒拋擲運移的輸送速度；還討論了筒式篩網的旋轉角速度對顆粒拋擲運動產生的影響。
  18. A new e. coli promoter - probe vector phn1005 was constructed by using a red - shift enhanced gfpmut3 as reporter gene and showed the following characters : 1, bamhi at the 5 " end of gfpmut3 structure gene could be used to clone promoter - active fragment and the strength of promoter could be quantitatively assayed. 2, a rrnbtlt2 terminator from rrna gene at the 3 " end of gfpmut3 could permit clone strong promoter. 3, another rrnbt1t2 terminator was inserted upstream bamhi to prevent reading through of promoters from puc19

    進一步以紅移且熒光強度提高21倍的gfpmut3為報告基因，構建了大腸桿菌啟動子探針載體phn1005 ，該載體上gfpmut3結構基因5 』端的bamhi位點可用來克隆具有啟動子活性的dna片段並定量分析插入的啟動子強度；其3 』端含rrnat1t2終止子，可允許克隆強啟動子；在bamhi上游同樣插入rrnat1t2終止子以防止載體puc19上的啟動子的轉錄通讀； gfpmut3結構基因上游還插入一段內含子序列使正反六種讀碼框的翻譯均可被終止，可保證gfpmut3以正確的讀碼框翻譯。
  19. 4. the seguence of cloned endostatin gene was confirmed with the dideoxy chain - termination method and is consistent with reported sequence of mouse endostatin

    4 .以雙脫氧末端終止法對重組質粒pbv220一endostatin進行測序，結果表明與己知小鼠endostatin基因序列一致。
  20. 3. construction of fusion genes with insecticidal protein gene and gfp the fusion genes was constructed by pcr. the pesticidal crystal protein gene crylac10 and gfp were chosen to construct the fusion genes

    建殺蟲晶體基因與gfp基因的融合基因pcr擴增全長gfp片段融合於去掉終止結構的殺蟲晶體蛋白基因的c -端，構建融合基因。
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