轉錄目錄 的英文怎麼說

中文拼音 [zhuǎn]
轉錄目錄 英文
duplicate catalog
  • : 轉構詞成分。
  • : Ⅰ名1 (用做記載物的名稱) record; register; collection; selections 2 (姓氏) a surname Ⅱ動詞1 (...
  • : Ⅰ名詞1 (眼睛) eye 2 (大項中再分的小項) item 3 [生物學] (把同一綱的生物按彼此相似的特徵分為幾...
  • 轉錄 : [電學] transcribe; transfer; [聲學] mixing; rerecording; [生物學] transcription; duplicating轉錄...
  • 目錄 : 1 (列出的事物名目) catalogue; contents; list 2 (書刊上列出的篇章名目) table of contents; cont...
  1. In my opinion, sun probably took this approach so that someone couldn t walk off with the javamail reference implementation that had many developers working on it transcribing public domain rfcs until the early hours of the morning and make boatloads of cash with it

    我認為, sun採取這種方法的的很可能是使其他人無法竊取javamail參考實現(曾有許多開發人員通宵達旦地將其到不受版權限制的rfc中)並籍此謀利。
  2. Function shows the duration and frequency of each behavior pattern, and the output file of the frequency contingency table. all saved files are in ascii format and can be read by most commercial word processors and statistics programs

    在分析功能方面,除了可計算每一行為的持續時間和發生頻率等基本數據之外,並可以把行為序列換成頻度關連表,再由
  3. Analyzing data " function shows the duration and frequency of each behavior pattern, and the output file of the frequency contingency table. all saved files are in ascii format and can be read by most commercial word processors and statistics programs

    在分析功能方面,除了可計算每一行為的持續時間和發生頻率等基本數據之外,並可以把行為序列換成頻度關連表,再由
  4. They are involved both in the production of mature proteins, acting as processing enzymes, and in the degradation of damaged or non - functional proteins [ 1 " 8l in plant plastids, proteases function in protein degradation seem to act to adjust the stoichiometry of subunits in supramolecular complexes, as well as to regulate the stoichiometry between different supramolecular complexes in response to environmental changes and process the nuclear - encoded preproteins in the stromal

    除了在相關蛋白質和翻譯方面的調控外,專一降解這些蛋白的蛋白酶活性以及翻譯量的上升也會加強對這些蛋白質的降解。雖然到前為止對光系統中蛋白酶的了解尚且不如對光系統中各種多肽以及蛋白色素復合體的了解,但是對類囊體和葉綠體中蛋白酶的研究已經進展到相當深度了。
  5. In this paper, a field strain of infectious bronchitis virus was isolated from proventriculus tissue, morphological observation by electron - microscope and the biological characterizations of the virus were studied, pairs of specific primers are designed and synthesized in correspondence with them, according to the published sequences of infectious bronchitis virus three structural protein ( spike protein s membrane protein m nucleocapsid protein n ) genes, the cdna of si gene, s2 gene, m gene. n gene of ib v isolate lx4 were amplified by rt - pcr and full sequences were first reported

    在此基礎上,根據國內外已發表的ibv基因序列,分別設計特異性引物,應用不同引物進行反合成cdna ,分片段對ibv的主要結構基因進行pcr擴增,並分別將各個的片段克隆到puc19載體上,在大腸桿菌dh5中實現的基因的分子克隆,經藍白斑篩選、限制性內切酶分析、 pcr鑒定,篩選出重組陽性質粒,並對各個的基因片段進行序列測定,從而獲得ibv主要結構基因全序列。
  6. This information is transcribed by the registrar into a draft entry of death registration.

    這個資料由登記員到死亡登記的收集條中去。
  7. Israelensis recombinants, which contained recombinants plasmid pmt4 and pmt9 respectively, were obtained by electroporation. the bioassay results showed that the recombinants b - pmt9 and b - pmt4 had toxicities both to resistant and susceptible c. quinqnefasciatus larvae during vegetative growth stage, having the lc ? o values similar to that of. fi. sssii - 1. however, the toxic levels of the final sporulated cultures of recombinants b - pmt4 and b - pmt9 differed, with a lcso value of 2 49mg / ml for b - pmt9 and little toxicity for b - pmt4 by using the plasmid pmt9, m txl gene from b. sphaericus was ligated with p20 and cytjaa gene, giving recombinant plasmid pmpx2

    含有pmt9和pmt4的大腸桿菌化子能表達產生mtx1毒素,發酵液對敏感和抗性致倦庫蚊幼蟲具有中度毒殺作用;含有pmt9和pmt4的蘇雲金芽孢桿菌化子b - pmt9和b - pmt4在營養體生長階段對敏感蚊幼和抗性幼蟲也具有毒性,毒力與野生型b . sss - 1相當,而不同化子在芽孢形成期的毒力因插入的mtx1基因方向不同而表現出差異,其中b - pmt4對標蚊幼毒力極低( lc _ ( 50 ) 10mg ml ) ,而b - pmt9對蚊幼蟲具有毒性( lc _ ( 50 ) = 2 . 49mg ml ) 。
  8. Given an unquoted identifier in the correct catalog case, returns the correct quoted form of that identifier, including properly escaping any embedded quotes in the identifier

    以正確的大小寫給定一個不帶引號的標識符,返回該標識符的帶引號的正確形式,包括正確義該標識符中嵌入的任何引號。
  9. You will not see the files in the directory you select, but all. jav and. java files in it will be converted

    您在所選中將看不到這些文件,但該中的所有. jav和. java文件都將換。
  10. Value - added tax ( vat ) of domestically made equipment will be returned in full amount if foreign - invested enterprises purchase equipment in china and the equipment belong to tax exemption catalogue, and income tax of these enterprises will be credited in accordance with relevant stipulations ; their fixed assets can be allowed for accelerated depreciation after approval of taxation organizations ; and business tax will be exempted for the income gained from technology transfer

    外商投資企業在國內購置設備,如該類設備屬免稅范圍,可全額退還國產設備增值稅並按有關規定抵免企業所得稅;經稅務機關批準,允許其固定資產加速折舊;取得的技術讓收入免征營業稅。
  11. By means of plant genetic engineering, foreign insects resistance gene can be transferred into plant cell. we cloned the cpti gene and transferred it into mustard by agrobacterium - mtdi & ted transformation method. and obtained the transgenic mustard plants. the main results are as follows : 1. isolation of cpti gene total rna was isolated from cowpea seedss cotyledons and leaves. the cpti gene fragment was amplified by rt - pcr using sequences of its two sides as primers

    本實驗是利用植物基因工程獲得抗蟲的基因芥菜植株,結果如下: 1豇豆胰蛋白酶抑制劑基因的分離分別提取豇豆種子、子葉及葉片的總rna ,逆成cdna 。以豇豆胰蛋白酶抑制劑基因兩端的序列為引物,用rt - pcr的熱啟動方法從上述cdna中擴增出的基因片斷。
  12. Two strains of prrsv were isolated from the swine infected with prrsv in shangdong province and daqing area, in order to clarify the source and genetic background of porcine reproductive and respiratory syndrome virus ( prrsv ) from different parts of china, thus providing theoretic basis for the study of vaccine against it. the prrsv was cultured on mark - 145 cells for 5 ~ ~ 6 passages. when the cpe was obvious, the virus was harvested and purified

    為了弄清我國不同地區prrsv的來源以及其遺傳學背景,為疫苗學研究提供理論根據,本研究在ch - 1a株完整的基因組獲得以後,從流行於我國山東( sd )和黑龍江大慶( dq )地區疑似prrs的豬體內分離到prrsv ,在mark - 145細胞上盲傳5 6代,細胞出現明顯病變以後,收獲病毒液,然後提純,提取全病毒rna ,經過反、 pcr擴增獲得結構基因orf2 7的的基因片斷,然後與pmd - t載體連接,化,得到陽性質粒后進行測序,並將其與ch - 1a株進行了比較分析,同時對這兩個毒株的結構基因組的理化性質進行分析。
  13. In order to use the responding ability to the inducers of pr - la promoter, two fragments, ip1 ( 900 bp ) and ips ( 603 bp ) were cloned from tobacco genomic dna by polymerase chain reaction ( pcr ) with primers designed according to the sequence reported in genbank. sequence analysis of the amplified 900 bp fragment indicated that the cloned sequence had 99 % of homology to the known sequence. its transcription start site, tata box and consensus sequence " tgac " conserved in pr genes were identical to those of pr - la promoter

    根據pr - 1a基因的報道序列,設計兩對引物,以煙草基因組為模板,通過pcr擴增得到900bp ( ipl )和603bp ( ips )兩個標片段,序列測定表明克隆的啟動子與報道序列具有99的同源性,起始位點、 tatabox及保守序列tgac與報道序列均完全相同。
  14. Mammalian cells are among the best systems for biopharmaceutical production due to their excellence in post - translational modifications. the products they produced are much more similar to their natural forms than those produced by prokaryotic, yeast or insect cells

    哺乳動物細胞表達系統具有準確的后修飾功能,表達的糖基化蛋白藥物在分子結構、理化性質和生物學功能方面最接近天然蛋白分子,是前重組糖蛋白藥物生產的首選體系。
  15. Once you have entered the virtual root for your web application, you have the option of specifying an application domain to enhance the way in which links are converted in your application

    當您輸入了web應用程序的虛擬根后,您就可以選擇指定應用程序域,以增強應用程序中的鏈接換方式。
  16. E. those foreign - invested projects, involving issues of quotas and license, belonging ot the restrictive projecs of the state s catalogue for the guide of foreing investment industries, and whose total investmentis above us $ 30 million, shall be submitted to the provincial and state s relative departments for examination and approval after the rcity s examination

    5 、投資總額在3000萬美元以上的項、涉及進出口放可證及配額管理的項,以及屬于《外商投資產業指導》中的限制類項,由新余市審核后報省和國家有關部門審批。
  17. Expression in vitro cos - 7 cells were transfected with pm, pms, pmi and pmsi constructs by cationic liposom, respectively. 48 hours later, mrna of targets gene were detected by rt - pcr and hil - 12 protein in culture supernatnant and cell lysates were detected by western blotting. p815 cells were transfected with pm and pms constructs and selected by g418

    2 .重組質粒在真核細胞中的表達: ( 1 ) pm 、 pms染cos一7細胞, 48小時后,用ri 』 - pcr檢測的基因在mrna水平的表達;染p815細胞, g418篩選抗性細胞克隆,用rt - pcr檢測的基因在mrna水平的表達,結果為陽性,說明在水平有的基因的表達。
  18. From the directory where you extracted the files, go to

    在解壓縮文件的中,
  19. The directory structure created in the process of conversion does not necessarily correspond to the directory in which the servlet was located in the original java - language project

    換過程中創建的結構不一定對應于原始java語言項中servlet所在的
  20. The most efficient regulation of gene occurs at transcription level by regulating the interaction between transcription factors and upstream regulation sequence. thus, to investigate promoter of a target gene will be helpful to predicate the principle of molecule regulation, biological function of molecule and even involving pathogenesis of some diseases

    水平是調控蛋白質表達效率最高的環節,通過影響相應的因子與啟動子和上游調控序列的相互作用調控的基因的表達,因此研究基因的啟動子對于了解基因的表達調控規律、闡明分子的結構和生物學功能乃至疾病的發生都有重要的意義。
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