表達標記 的英文怎麼說

中文拼音 [biǎodábiāojì]
表達標記 英文
presentation markup
  • 表 : Ⅰ名詞1 （外面;外表） outside; surface; external 2 （中表親戚） the relationship between the child...
  • 達 : Ⅰ動詞1 （暢通） extend 2 （達到） reach; attain; amount to 3 （通曉; 明白） understand thoroughly...
  • 標 : Ⅰ名詞1 [書面語] （樹梢） treetop; the tip of a tree2 （枝節或表面） symptom; outside appearance; ...
  • 記 : Ⅰ動詞1 （把印象保持在腦子里） remember; bear in mind; commit to memory 2 （記錄; 記載;登記） writ...
  • 表達 : deliver; express; show; voice; convey; communicate
  • 標記 : （標志; 記號; 貨物標記） tab; sign; stamp; peg; label; mark; flag; blip; notation; fleck; track; ...
  1. By tagging the oxt gene with a gfp tag, it was found that this gene mainly expressed in the cytosol

    通過把。 xt基因加上gfp標記，發現該基因主要在細胞質中表達。
  2. Furthermore, the wing imaginal disc clonal analysis showed that in the homozygous sll mutant clones, the extracellular wg was dramatically reduced. the reduction of extracellular wg indicated that the wg signaling in the wing imaginal disc was disrupted. the reason leaded to this phenomenon is that sll encodes a paps transporter, so the disruption of the sll gene would generate the unsulfated heparan sulfate proteoglycan ( hspg ), which most likely would lose normal function

    進一步結合運用flp - frt系統和minute ~ - ，用缺損myc蛋白的表達來標記純合的sll突變基因克隆，用minute ~ -來相對的擴大含sll突變基因的克隆，對翅成蟲盤所作的克隆分析表明，在含sll突變基因的克隆中，細胞外的wg蛋白分佈明顯減少，這種細胞外的wg蛋白減少表明在翅成蟲盤中wg信號傳導受到了明顯抑制。
  3. As it ' s proprietary, a large numbers of bibliography resource ca n ' t be provided to common readers of internet. along with the development of network technology, it has a instancy need to conversion marc format to the information that the browser can recognize. the language xml not only can expresses the metadata, but also can show the content of data. lt can provide individuation page layout

    Marc格式是目前圖書館館藏資源的主要表示格式，由於其專用性，使得目前大量的書目資源無法通過一般的搜索引擎向internet用戶提供，隨著網路技術的不斷發展，迫切需要將marc格式的數據轉換成常用瀏覽器所能識別的信息，為大眾提供服務，可擴展標記語言xml不僅可以表達元數據，而且可以揭示數據的內容，提供個性化的頁面顯示，用xml語言對marc數據進行描述是解決這一問題的有效途徑，文章提供了marc數據的xml表示方法和實現途徑。
  4. This thesis will rely on previous studies of instructions on the general rules and language functions, and modification of teacher talk to carry on a multi - layer study on junior middle school teachers " instructions with aspect of linguistic forms and language functions in chinese efl classrooms. after study on the transcriptions of 30 lectures ( 10 lectures are given by in - service teachers, 10 lectures are given by pre - service teachers and 10 lectures are given by the winners in fine - quality classroom competitions ) of efl classroom of junior middle schools in china, the major findings are : ( 1 ) the teachers likely use some devices with respect to prosody ( temporal variables ), lexis, syntax and discourse to simplify and clarify the complex instructions to match the requirement of junior middle school students " listening comprehension. ( 2 ) there are about three factors that cause the ineffective instructions

    本文在前人的關于教師語言的調整，指令語及其表達功能的研究基礎上以何安平教授建立《中學英語教育語料庫（ mstm ） 》中的近17 . 7萬字的子語庫《英語課堂教學語料庫（ msee ） 》為研究語料，選擇了其中30節初中英語課為研究對象，對教師指令語的言語形式及其語言功能進行了較為深入的描述分析，發現： （ 1 ）在音律層面，中國中學英語教師習慣川停頓來放慢語速或在一些難詞之前做停頓以便達到讓學生理解的要求：詞匯層面，教師慣用一些表達方式來給指令語；句法層面，教師也是盡量用簡單句來簡化指令語；語篇層面，初中英語課堂上教師常用一些信號詞來起始解釋性指令語，並少用宏觀語篇標記詞來幫助學生理解，但卻常用微觀語篇標記詞來吸引學生的注意力。
  5. In summary, we should investigate the more efficient cultural system for mammary orgnoids in vitro for enriched more mammary epithelial stem cells, and to screen the expression profiles in mammary epithelial stem cells to discover the specific marker for mammary epithelial stem cells in order to utilize the model of mammary epithelial stem cells to regenerate transgenic mammary glands in cow or sheep for human health, to uncover the mechanism of organogenesis, and differentiation

    在此之前，仍然只能以造血幹細胞的特異性表達抗原scal - 1作為一個標記，進行類乳腺幹細胞的分析和分選研究。進一步研究類乳腺幹細胞的特異性表達譜，以期能夠找到類乳腺幹細胞的特異性表達抗原，分離得到類乳腺幹細胞，作為發育生物學和再生生物學研究的模型。
  6. Methods : ( 1 ) the segregation of foreign target gene in the t1 by histochmical gus assays ; ( 2 ) identification of pure line from transgenic tomatoes ( tl ) through examining gus expression in pollens in conjunction with pcr analysis of marker gene ( npt ) ; ( 3 ) the transcript levels of leetrl or leetr2 in anti - sense transgenic plants ; ( 4 ) the phenotypes of the transgenic plants in tomato during whole life cycle under ethylene - treated and non - treated conditions

    本研究以反義乙烯受體leetr1 ， leetr2基因番茄t _ 0代種子為實驗材料，利用gus基因表達研究外源基因的遺傳規律，並藉助于pcr技術對目的和標記基因的鑒定獲得轉基因t _ 1代材料。利用gus基因在t1花粉中的表達鑒定獲得轉基因純合植株。研究了轉基因後代的生長發育模式、對外源乙烯敏感性，以及靶基因的表達特性，初步探明了它們在乙烯受體系統中的功能。
  7. Marks the beginning of a quantifier expression

    標記限定符表達式的開始。
  8. We find the chimeric protein in leaf epidermal cells, stomatal guard cell and root epidermal cell. actin filaments can be visualized clearly in guard cell, in guard cells of open stomata under light, actin filaments arrange reticulate randomly in cytoplasm. in guard cells of closed stomata under darkness, actin filaments arrange curly along the longitude of guard cell

    在葉片的表皮細胞、保衛細胞、根部的皮層細胞中有融合蛋白的表達，保衛細胞中微絲標記狀況良好，經光誘導處于開放態的氣孔的保衛細胞微絲呈網狀結構，在細胞內無規則分佈；經黑暗誘導處于關閉態的氣孔保衛細胞中微絲束沿保衛細胞縱軸排列，呈捲曲狀分佈。
  9. We constructed a binary vector carrying a modified human afgf gene and a mana gene that allows the use of pmi selection system, an antibiotic and herbicide - free system, during the transformation procedure

    我們構建的雙元表達載體帶有一個經過改構的人類酸性成纖維細胞生長因子基因（ afgf ） ，載體上的選擇標記基因為mana ，它使得轉化過程中可以使用pmi這種不含抗生素及除草劑的選擇系統。
  10. However, some people dislike dtd for its awkward syntax, limitations in the text and markup constructs it can express, and the difficulty of handling xml namespaces

    但是，一些人不喜歡dtd ，因為它醜陋的語法、表達文本和標記結構的局限性，並且難以處理xml namespaces 。
  11. Marks the beginning and end of a subexpression

    標記子表達式的開始和結束。
  12. In this study, in order to examine the dynamics of tip [ ca2 + ] i together with the dynamics of tip - localized f - actin in vivo, a kind of double labeled material was constructed. the ca2 + and actin microfilaments of arabidopsis pollen tubes were labeled by cameleon and gfp - mtalin respectively

    本研究以擬南芥花粉管為材料，通過轉基因技術，將分別標記ca ~ （ 2 + ）和微絲的兩種熒光蛋白cameleon與gfp - mtalin在花粉管中同時表達，實現活體花粉管中ca ~ （ 2 + ）與微絲的同時標記。
  13. Owl ' s semantics is limited to description logic, which cannot capture semantics of arbitrary rules. therefore, owlrule + is designed. its syntax extends owl and its semantics is based on carin, a representation language combining description logic and horn rules

    針對語義web層次結構中webontology語言owl在一般規則表達能力方面的不足，在其基礎上設計了一種語義web規則標記語言? ? owlrule + ，作為語義web的邏輯規則層。
  14. Total cellular rna were extracted, 40 micrograms of the total rna were used in the reverse transcription reaction, using superscript ii reverse transcriptase, oligo ( dt ) i8 primers, and cy3 - dctp or cy5 - dctp for the experimental and control group respectively. the labeled cdnas were hybridized to microarrays at 42c for 12 h - 18 h

    提取as _ 2o _ 3作用k562細胞前後的總rna ，用superscript逆轉錄酶逆轉錄成cdna第一鏈，並在逆轉錄的過程中，用cy3 cy5熒光染料分別標記對照組處理組，與自製的k562細胞基因表達譜晶元雜交。
  15. Green fluorescent protein ( gfp ) gene was conjugated to the 3 " end of the pap gene in order to screen easily of the transgenic cotton plants. the combined gene was cloned into plant expression vector pbi121 and then transformed. about 5000 seeds of the transgenic cotton were obtained and the some seedlings of the transgenic cotton could give a bright green fluorescence in the dark condition when the cotton seedlings were irradiated with ultraviolet rays

    為了便於轉基因棉花後代的篩選，在pap基因的3 』端融入了綠色熒光蛋白gfp ）基因，然後將融合基因克隆在植物表達載體pbi121上，再進行遺傳轉化，得轉基因棉花種子5000餘粒，將種子播種長到于葉展開時，先在黑暗中用紫外燈照射，查找表現綠色熒光的幼苗，然後再用地高辛（ dig ）標記的pap基因特異性探針對這些棉花進行點雜交，最後發現有8株棉花表現陽性反應，說明pap基因的確己經轉到了棉花的基因組中，其棉花黃萎病的抗性鑒定正在進行之中。
  16. One was cloning, sequence analysis and expression of the fragment containing the b and c antigenic sites locating at the 5 " terminus in spike gene of tgev in prokaryotic expression system ( fused with gst ), the other was preparation of non - radioactive probe labeled by digoxigenin for detecting the rna extracted from tgev by assay of dot - blot

    為了鑒別診斷tgev與prcv及對tgev進行流行病學調查，本研究採用原核表達系統（ gst融合表達系統）表達tgev纖突蛋白（ s蛋白）中含有b和c抗原位點的多肽，並且制備了非放射性地高辛標記的核酸探針，通過斑點雜交（ dot - blot ）檢測tgev核酸rna 。
  17. 4. we use half quantification and digoxigenin detection to investigate the expression pattern of ent - kaurene oxidase. we found that it was regulated by development, it expressed high in the fast growing tissue, expanded leaves under a fast growing circumstance also express high level of ent - kaurene oxidase

    利用半定量rt - pcr的方法結合地高辛標記法，貝殼杉烯氧化酶在果樹中的表達是受發育調控的，其在旺盛生長的組織中表達量高，在植株旺長期的成年葉中表達量也很高。
  18. In ddmm, the rdb is taken as the bottom storing medium and the upper xml view is set up for data exchange and direct application under internet / intranet environment. based on ddmm, the multi - tiered and bi - directional data integration technique between xml and rdb, is studied systematically and in detail, and the reciprocal data accessing and exchange between rdb and xml is carried out on respectively three levels : static data transformation, dynamic data query and synchronized data update. the infrastructure for manufacturing informationlization will certainly be internet / intranet, and xml has been a factual standard for data representation under internet / intranet environment

    製造業信息化的基礎平臺將是internet intranet ， xml （ extensiblemarkuplanguage ，可擴展標記語言）已經成為internet intranet環境下數據表達的事實標準，而目前企業大量數據仍存在於佔主導地位的關系數據庫（ relationaldatabase ，簡稱rdb ）中，如何在rdb與xml之間架起數據交換與數據操作的橋梁，已成為製造業在internet intranet環境實現信息化迫切需要解決的突出問題之一。
  19. The env protein deduced from env gene encodes the hydrophilic surface protein ( su ) and the hydrophobic transmembrane domain ( tm ) that determine the specific interaction between virus particles and cell surface receptors during retroviral entry. the su of retroviruses is a highly variable genetic element, containing receptor binding sites and major antigenic determinants. exjsrv - specific dna probes were derived. by using these dna probes in tissue hybridization. we successfully identified jsrv mrna expression and proviruses dna in sheep lung tissues infected with jsrv and control group has no postive signals, validating the use of exogenous virus - specific dna probes in the analysis of oncogenic proviral integration sites and identification of integrated exogenous proviral sequences

    用地高辛隨機引物法標記exjsrv特異的env片段，制備探針，原位雜交檢測spa肺組織中的rna及前病毒dna ，結果表明spa患羊肺組織內有jsrvenv基因mrna的表達，同時也檢測到了前病毒dna ，而相應的陰性對照卻無陽性信號，證實外源性病毒特異的dna探針在致瘤性前病毒的整合位點和整合的外源性前病毒的檢測中具有可信度。
  20. In order to further investigate the role of axudl in human tumor carcinogenesis and the potential association between the axudl gene expression status and the stimulation of transforming growth factor beta in human cancers, the present study was performed in three aspects as follows : ( 1 ) cloning full length enconding region cdna of axudl and construction of eukaryotic vector that expression the fusion protein of axud1 and influenza virus hemagglutin ha epitope tag ; ( 2 ) exploring the time and dose effects of tgf - 1 on the expression - of axudl gene in hepg2 hepatoma cells and spc - a1 lung carcinomas cells, and studying the effects of overexpression of axud1 on the expression of cell cycle and apoptosis related protein in hepg2 hepatoma cells ; ( 3 ) construction and expression of human axudl in e. coli m15. the following main results and conclusions can be obtained from the present study : 1. the full length ecnoding region of human axudl cdna from human peripheral blood lymphocytes was successfully cloned using one step rt - pcr method, and constructed into a eukaryotic expression vector which can be expressed a ha - axud1 fusion protein with axud1 and influenza virus hemagglutin ha epitope tag. the recombinant plasmid was identified by polymerase chain reaction, restriction endonuclease maping and sequencing, this expression vector might be instrumental to further study the function of axud1 protein in tumor cells

    為了進一步研究axud1在人類腫瘤發生中的作用及axud1基因的表達狀況與tgf -介導的信號通路的關系，本實驗研究分為三個部分： （ 1 ） axud1基因cdna全長編碼區的克隆和ha表位標記的axud1基因表達載體的構建； （ 2 ）探討肝癌細胞hepg2和肺腺癌spc - a1細胞中tgf - 1誘導的axud1基因表達的時間、劑量效應以及誘導表達的可能機理，並研究axud1的過表達對細胞周期和細胞凋亡相關蛋白表達的影響； （ 3 ） axud1原核表達載體的構建及其在大腸桿菌中的表達。本實驗的主要結果和結論如下： 1利用一步法rt - pcr成功地從人類外周血淋巴細胞中克隆出axud1基因編碼區cdna ，並將其構建入真核表達載體中，編碼的ha - axud1融合蛋白帶有流感病毒凝血素ha的表位標記肽段。
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