重組體 的英文怎麼說

中文拼音 [zhòngzǔtǐ]
重組體 英文
recombinants
  • 重 : 重Ⅰ名詞（重量; 分量） weight Ⅱ動詞（重視） lay [place put] stress on; place value upon; attach im...
  • 組 : Ⅰ名詞1 （由不多的人員組成的單位） group 2 （姓氏） a surname Ⅱ動詞（組織） organize; form Ⅲ量詞（...
  • 體 : 體構詞成分。
  • 重組 : bpr
  1. First, to construct a recombinant plasmid pegfp - c - fos with c - fos promoter and egfp, and then transfect it into human bladder transitional cell carcinoma biu - 87 cell ; second, based on the changes of the expression of gfp in the biu - 87 cell which induced by the aconitine and hab toxins, the concentration of the hab toxins could be detected

    目的：構建一個含c - fos啟動子和egfp報告基因的pegfp - c - fos重組質粒載體。體外轉染膀胱癌biu - 87細胞后，利用赤潮毒素作用后細胞表達綠色熒光蛋白的變化來檢測赤潮毒素，初步建立一種以細胞為基礎受體水平的赤潮毒素檢測方法。
  2. The second section described the accounting issues brought by cyber economy environment including the impact to the accounting suppose, accounting target, the content, the means, the process of accounting checking and the impact to the accounting information system. the third section described the ideas of the innovation of cyber economy environment emphases on the accounting business process reengineering, accounting information system innovation, assets affirmance, accounting settlement under the cyber economy environment. on basis of the third section, the fourth section analyzed the cyber accounting ' s origins, developme nt, characteristic and problems occurred in the development of the cyber accounting

    本文共分四章，第一章論述了網路經濟環境下會計環境的變遷，分析了網路經濟的產生與特點，概述了電子商務及虛擬企業的特徵，並指出對企業的組織、生產、管理環境帶來的巨大變化；第二章闡述了網路經濟環境引發的會計問題，包括對會計假設、會計目標、會計核算內容、方法、流程及會計信息系統的影響；第三章提出了對網路經濟環境下的會計創新的設想，重點論述了網路經濟環境下的會計業務流程重組與會計信息系統的變革，網路經濟環境下的資產與會計確認，以及會計結算等方面的創新設想；在第三章討論內容的基礎上，第四章具體分析了網路會計的產生、發展及特點，並分析了網路會計發展過程中存在的主要問題，針對這些問題，提出了相應的對策。
  3. The total rna was isolated from pokeweed ( phytolacca americana ) leaves using the method of guanidine isothiocyante and used as template to amplify the total length and deleted mutant pokeweed antiviral protein ( pap ) gene by rt - pcr and then the pap gene was cloned into pgem - t vector. the sequencing results showed that pap gene had 99. 9 % identity comparing with the pap gene nucleotide sequence reported by lin et al ( 1991 ). the iptg - inducible expression vector containing the pap gene was constructed and transferred into e. coli bl21 ( de3 ) - plyss

    將缺失型pap基因克隆到植物表達載體pbi121中，通過液氮冷凍法將重組質粒轉入農桿菌lba4404細胞中，然後採用葉盤法，在該農桿菌的介導下將pap基因導入普通煙草中，經過卡那黴素抗性篩選，最後獲得了轉pap基因的工程煙草植株，摩擦接種煙草花葉病毒（ tmv ） ，與非轉基因煙草相比，能夠推遲癥狀表現達2月之久，說明pap基因能夠在其它植物體內產生有活性的高抗病毒的蛋白質。
  4. We need a comprehensive assessment of the recombinant dna issue, preferably under the auspices of the federal government.

    對于重組體DNA問題，我們需要有一個全面的估價，而且最好由聯邦政府主辦。
  5. Recombinant dna is also an excellent example of this problem.

    重組體DNA也是這類問題的一個極好的例子。
  6. We presented the history of recombinant dna research and our guidelines, and invited the committee's opinions.

    我們介紹了重組體DNA的歷史和我們的準則，並徵求這個委員會的意見。
  7. Interaction with doc - 1r and cdk2 proteins under physiological condition using cotransfection, coimmunoprecipitation and western blotting, we have transfected the plasmids into 293 cells according to following combination : pc

    分別將正、反義小鼠doc一ir重組體命名為pedna3一doc一ir +和pedna3一doc一ir一。
  8. Cryptogrammic chip introduced in this paper has been tested on the altera ' s apex20ke fpga. the main clock frequency reached 40mhz. the chip includes 30, 000 les. in order to utilize esb resource in altera ' s chip, we adopted embedded rom and ram and can realize the function of whole system with only one chip. lt is the embodiment of methodology and notion of sopc ( system on a programmable chip ). the simulation of this cryptogrammic chip proves the correctness of function of the chip, which shows that the important ideology based reconfigurable architecture has special significance in designing of cryptogrammic chip

    本文所闡述的密碼晶元在altera公司的apex20kefpga上進行了測試。工作頻率達到了40mhz ，佔用了3萬個le . ，利用altera器件的esb資源，採用內置ram和內置rom設計方法，用一片晶元即可實現整個系統的功能，充分體現了sopc的設計方法和理念，對晶元的模擬和測試均證明晶元功能正確，表明基於可重組體系結構這一重要思想在密碼晶元設計中具有特殊的意義。該晶元的設計遵循hdl設計方法學的一般方法。
  9. This paper systematically presents the whole design process of a cryptogrammic chip based on reconfigurable architecture. firstly it begins with a brief introduction to the background of the cryptogrammic chip design, and it clearly states the characteristic and the researching thoughts of cryptogrammic chip design with hdl. then the design environment and cipher algorithms are introduced briefly

    本文系統地論述了基於可重組體系結構的密碼晶元設計的全過程，文章首先闡述了該設計的課題背景，給出了使用hdl方法設計密碼晶元的特點和研究思路，然後對晶元的設計環境作了簡要說明，並對密碼演算法進行了簡單介紹。
  10. The 496 bp fragment of the orf of p22 gene and a 561 bp fragment were amplified from the genomic dna of zs strains of toxoplasma gondii. both 496 bp and 561 bp fragments were successfully cloned into the plasmid pthiohisa, b, c and pbudce 4. 1 respectively. 2

    從弓形蟲zs株基因組中擴增出p22編碼基因的一長496bp ，另一長561bp的片段，並成功構建含p22編碼基因的原核質粒重組體pthiohisa ， b ， c / p22 ，及真核重組表達質粒pbudce4 . 1 / p22 。
  11. An expression vector with fragment 9 in antisense orientation was constructed to block the expression of the relevant gene ( fragment 9 related gene, fnr gene ) in vero cells. interestingly, we found that the nontargeted mutation frequency induced by mnng was increased significantly, implicating that the product of the blocked gene may be involved in the inhibition of nontargeted mutation

    利用反義核酸技術構建含反向插入9號片段的真核細胞表達重組體並轉染細胞，以獲得反義rna阻斷vero細胞中相應基因的表達，發現mn 』 ng誘發的非定標性突變頻率顯著增高，提示被阻斷的相關基因的表達產物可能參與抑制非定標性突變的發生。
  12. In this paper, the methodology and implementation with hdl of design based reconfigurable architecture are discussed in detail, which includes the implementations of algorithms circuit, register file with controllable node, decoder, interface and main controller. from the introduction of design process of every module circuit, we can see easily some general feature of vlsi design with hdl

    在此基礎上詳細討論了基於可重組體系結構的密碼晶元設計方法和各電路實現的結構圖，包括演算法電路、可控節點寄存器堆、譯碼電路、介面電路和主控模塊電路等。通過對各個模塊設計過程的介紹，闡明了使用hdl語言設計超大規模集成電路的一般特點。
  13. Rhbmp - 2 standard test method forin vitro biological activity of recombinant human bone morphogenetic protein - 2 rhbmp - 2 using the w - 20 mouse stromal cell line

    使用w - 20老鼠基質細胞系的重組體人骨形態形成蛋白- 2
  14. The construction of pci - il - 2 : primers were designed by the software oligo, xhol and sail were added to the primers, the cdna of il - 2 was obtained by pcr. the cdna of il - 2 was ligated with pci - neo cleaved by xhol and sail. the recombinant was evaluated by pcr

    Pcr法擴增幾億片段，在t4連接酶的作用下與xhol和sal工酶切的pci neo載體連接， pcr法鑒定重組體，用xho工， xhol sal ， ban工工酶切進一步驗證重組體，命名為pclll 2 。
  15. After transformation, we have chosen the positive bacterium clones by bacterium colon pcr. with dna sequencing, we have made sure direction of dna sequence which inserted into the plasmid and have named sense and antisense reconstruction plas - mids respectively

    採用sanger雙脫氧末端終止法再進一步進行dna序列測定分析，檢測doc一1rcdna序列插人表達載體的方向，確定正、反義重組體。
  16. Construction of prokarocyte expression recombinant of human thymosin 1 and its expression in escherichia coli

    1原核表達重組體的構建及其在大腸桿菌中的表達
  17. Recombinant dna is also an excellent example of this problem

    重組體dna也是這類問題的一個極好的例子。
  18. According to the result of sequence analysis, the pcr product was subcloned to form cd40 / pcdna3

    雙酶切法進行鑒定，並利用t7引物鑒定重組體cd40 pcdna3的方向。
  19. We presented the history of recombinant dna research and our guidelines, and invited the committee ' s opinions

    我們介紹了重組體dna的歷史和我們的準則，並徵求這個委員會的意見。
  20. We need a comprehensive assessment of the recombinant dna issue, preferably under the auspices of the federal government

    對于重組體dna問題，我們需要有一個全面的估價，而且最好由聯邦政府主辦。
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