轉運片段 的英文怎麼說

中文拼音 [zhuǎnyùnpiānduàn]
轉運片段 英文
transport piece
  • : 轉構詞成分。
  • : Ⅰ動詞1 (物體位置不斷變化) move; revolve 2 (搬運; 運輸) carry; transport 3 (運用) use; wield...
  • : 片構詞成分。
  • : Ⅰ量詞(部分) section; segment; part; paragraph; passage Ⅱ名詞(姓氏) a surname
  • 轉運 : 1 (運輸) transport; transfer; transship 2 (運氣好轉) have a change of luck; luck turns in one...
  • 片段 : part; passage; fragment; extract; segment; bit; episode; snatch; section
  1. Third, it is this " moment " of the segment of space - time which based on the the philosophy of the nature and describing the mechanical movement that symbolize the transform from the view of integralization in classical atomism of mathematics to the view of integralization of modern real number

    另外,正是基於新的自然哲學的、作為描述機械動的時空的「瞬」標志著古典數學原子論的積分觀向現代的分割實數連續統的積分觀的化,而現代數學的微分概念更是直接源於描述機械動的速度和與動軌跡密切相關的曲線的切線問題。
  2. The result showed that the homology rate of pila gene among the 5 avian pathogenic e. coli strains tested and one human e. coli were from 89. 8 % to 91. 1 %, and the homology rate of amino acid were from 88. 5 % to 91. 8 %. the homology rate of pila gene sequence among 5 avian pathogenic e. coli strains tested and avian pathogenic e. coli reported ( serotype o1, o2, o78 ) were from 87. 8 % to 90. 2 %, and the homology rate of amino acid were from 84. 6 % to 91. 2 %. there had homology in avian pathogenic e. coli. there had some common antigen side in type 1 pili of avian pathogenic e. coli

    結果表明:用msha法檢測1型菌毛的檢出率為80 ( 36 45 ) , pcr法的檢出率為95 . 5 ( 43 45 ) , pcr方法用於1型菌毛的檢測比msha更加敏感、快速、特異性強;選擇5株優勢血清型雞源致病性大腸桿菌代表株( o _ ( 89 ) , o _ ( 119 ) , o _ ( 141 ) , o _ ( 127 ) )的1型菌毛pila基因的pcr擴增經純化后,分別定向克隆到puc18質粒的多克隆位點,構建了含有目的基因的克隆質粒,並化到dh5株大腸桿菌載體菌中,篩選獲得陽性克隆菌株。
  3. 705bp dna fragment of mxnrampl gene and full cdna of mxlrtl gene which were related to resist iron stress were cloned by using malus xiaojinensis cheng et jiang - the first iron - efficient genotype in the genus malus in the world as material. ( 1 ) using fragment of nramp gene from wheat and fe ( ll ) - transporter gene fragment of maize ( zmlrt ~ ) as probes, we analysed these genes by blotting hybridization technique in malus xiaojinensis cheng et jiang

    本實驗以中國農業大學園藝植物研究所篩選到的一個蘋果鐵高效基因型? ?小金海棠( malusxiaojinensischengetjiang )為試材,分別克隆了小金海棠的抗缺鐵相關基因mxnramp1基因的752bp基因組dna和fe ( ) -蛋白基因( mxirt1 )的cdna全長,為深入探討小金海棠抗缺鐵的分子機理奠定了基礎。
  4. Based on the conclusion of organizing into trains and simulating the thoughts of dispatchers in district stations, this paper analyzes the features of time sets of shunting locomotives, constructs the reasonable graph model in the way of making out time sets, and converts it into the problem of graph coloring

    在車流推算的基礎上,從應用計算機模擬區站調度員思維的角度出發,通過分析車列佔用調車機車時區集合的特點,使用劃分時間的方法建立合適的調車機車安排的圖論模型,將調機用問題化為頂點具有加權的圖的k -著色問題。
  5. The study was undertaken to isolate fe ( ii ) - transporter cdna and related binding protein cdna under fe - deficiency stress from a fe - deficiency root cdna expression library of malus xiaojinensis by screening library using maize fe ( ii ) - transporter cdna and wheat tamre - bp cdna as a probe. the main results as follows : 1 out of approximately 120000 plaques, four positive cdna clones encoding fe ( ii ) - transporter proteins, designated pftl -

    本試驗以蘋果屬小金海棠( malusxiaojinensischengetjiang )為試材,利用玉米fe ( )蛋白基因以及小麥金屬反應元件結合蛋白tamre - bpcdna為探針,篩選小金海棠缺鐵根cdna表達文庫,目的在於克隆蘋果鐵高效基因型小金海棠的fe ( )蛋白基因以及與缺鐵脅迫相關的結合蛋白基因。
  6. One of them was identified as the beth gene of halobacillus sp. d8. a hydrophobicity plot of beth revealed an alteration of hydrophobic and hydrophilic segments that was characteristic for integral membrane protein, suggesting the presence of 12 transmembrane - spanning segments and belonged to bcct family

    將重組質粒測序,插入大小為4kb左右,通過blast比較,結果顯示含有三個orf框,其中一個為甘氨酸甜菜堿蛋白,對其氨基酸組成進行疏水性分析,推測為含有12個跨膜域的跨膜蛋白,屬于bcct家族。
  7. ( 3 ) 490bp cdna fragment of fe ( ii ) - transporter gene mxlrtl was cloned by using common pcr method from iron - stressed root cdna library of malus xiaojinensis cheng et jiang with primers designed according to the conserved domain sequences of plant irt gene families. then we cloned the full cdna of mxlrtl gene by race method from this library with primers designed according to the sequence of 490bp cdna fragment

    ( 3 )根據植物irt基因家族的功能保守區序列設計引物,首先通過常規pcr法從缺鐵脅迫處理的小金海棠根系cdna文庫中克隆了fe ( ) -蛋白基因mxirt1的490bp的,然後根據測序結果設計引物,通過race法從該cdna文庫中克隆了mxirt1基因的cdna全長。
  8. The emphasis of this article is the design in the second period, which is based on the pic microchip interface, because at present embedded structure is adopted by most of medical instruments so that it can run separately without computer, hi this part the article specifically introduces the interface circuit of pic16f877 single - chip, which includes the acquisition of a / d signa ls and the serial communication between the single - chip and computer, the design of complex programmable logic device ( cpld ) and the using of hardware describe language ( vhdl ) to control the rotate speed of 4 - route stepping motors

    本論文的重點是在設備的第二階開發,它是基於pic系列單機介面的硬體設計,主要是針對現階大多數醫療設備都是採用嵌入式結構,它能夠脫離計算機單獨行。在這部分詳細介紹了pic16f877單機的外圍電路,包括a d信號的採集、單機與計算機的串列通信,可編程邏輯器件cpld硬體的設計,以及用硬體描述語言vhdl編程來同時實現4路步進電機的速控制。
  9. 2 sequences were analysed and compared in genbank : ptfl is 494bp and ptf2 is 763bp in longth, the deduced proteins consist of 88 and 172 amino acids respectively, these cdna - clones encode the same gene - fe ( ii ) - transporter. 3 southern blotting showed that fe ( ii ) - transporter was a single copy in malus xiaojinensis genome and it was also existed in malus baccata and malus zumi

    2 、根據測序的結果,將所得序列在genbank中進行同源性比較,結果如下: ptf1長為494bp , ptf2長為763bp ,分別編碼88個和172個氨基酸,屬于小金海棠fe ( )蛋白基因的兩個不同長度的基因,是同一個基因。
  10. The control system adopts high capability singlechip, aduc812 ( 8052 - compatible core ). it can expediently achieve a / d ( 12bit ), d / a ( 12bit ), phase compensation of the rotor position singles, and speed closed - loop control, and fully resolves the well - off switch from the out - synchronization to the in - synchronization. the practical prototype of the system is developed for the control of a dentist " sensorless brushless dc drill motor

    系統採用高性能aduc812 (兼容8052內核)單機作為微處理器,方便的實現a / d ( 12位) 、 d / a ( 12位) 、電機子位置信號相位檢測與補償以及系統速度閉環控制,很好地解決了無位置傳感器bldcm從外同步行階到內同步行階的順利切換。
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