模板鏈 的英文怎麼說

中文拼音 [móbǎnliàn]
模板鏈 英文
template strand
  • 模 : 模名詞1. （模子） mould; pattern; matrix 2. （姓氏） a surname
  • 板 : Ⅰ名詞1 （片狀硬物體） board; plank; plate 2 （專指店鋪的門板） shutter 3 [音樂] （打拍子的樂器） ...
  • 鏈 : Ⅰ名詞1. （鏈子） chain Ⅱ動詞（用鏈栓住） chain; enchain Ⅲ量詞（計量海洋上距離的長度單位） cable length
  • 模板 : [土] formwork; mould; shuttering; follow board; form board; match board; match plate; mother plat...
  1. Degenerate oligonucleotides to highly conserved regions of cucumis melo 1 - aminocyclopropane - 1 - carboxylic acid ( acc ) oxidase gene were used to prime the amplification of fragment of 128bp by ploymerase chain reaction ( pcr ) in samples of genomic dna from fruit of cucumis melo l. cv hetao flesh, which was cloned into plasmid vector pmd - 18 - t. the clon of antisense orientation were selected, and it was inserted downstream of camv35s promoter and enhancer " " of tmv into the plant expression vector pbinyxw, antisence expression vector pbinya was constructed. at the base that pollination and fertilization of cucumis melo l. cv hetao was studied, using pollen tube pathway transformate cucumis melo l. cv hetao, 76 fruit had been obtained, moreover, hardness and content of sugar were analysed

    本實驗以河套蜜瓜果肉基因組dna為模板，用甜瓜acc氧化酶基因特異寡核苷酸鏈為引物進行pcr擴增，得到128bp的擴增產物。將得到的擴增產物克隆到質粒載體pmd - 18 - t上，篩選反向克隆，然後將其反向構建到植物表達載體pbinyxw的camv35s啟動子和tmv增強子「 」的下游，構建成反義表達載體pbinya 。並在對河套蜜瓜授粉受精生物學研究的基礎上，通過花粉管通道法轉化河套蜜瓜，共獲76顆瓜，並進行了硬度和含糖量的分析。
  2. Abstract : duri ng concrete deep well constructi on ， because of thediffi culti es i n engi neeri ng geographi cal conditi ons ， the ordi nary bilateral hydrauli c sli di ng formwork technology can not be adopted. therefore ， an unilateral sli di ng formwork technology lifted by chai n block method can beappli ed to advantage and better solved the proble m

    文摘:在混凝土深井施工中，由於受地理環境的限制，不能內外安裝模板時，難以應用一般的液壓滑模施工技術，而採用單面模板、鏈條葫蘆提升滑模工藝，可較好地解決這一問題。
  3. Guan xiaohong ( 1991 ) established a cell line of the monoclonal anti - idiotypic antibody ( anti - id ) np30 of schistosoma - 6 - japonicum, whose isotype was identified to be igm and which was testified to be internal image of gaa

    分別以日本血吸蟲單克隆抗獨特型抗體wbo的雜交瘤細胞株總基因組dna和其提取rna進行rticr合成的cdna第一鏈為模板，擴增v 。 、 v 。
  4. New five - stage cyclone pre - heater system, high efficiency air girder grate cooler, multi - passage pulverized coal burner, davison heat temperature fan, luqi bs930 electrical dust collector, as well as chain - board elevator, chain conveyor adopted in this production line can ensure that the technology is advanced compared to other production lines with the same scale

    如新型五級旋風預熱預分解系統、高效空氣梁篦冷機，節能型多通道噴煤管，戴維森高溫風機，魯奇最新技術生產的電收塵（ bs930 ）等，輸送設備採用了耐用、節電的板鏈提升機、鏈式輸送機，將使本工程的裝備在同規模生產線中處于領先水平。
  5. A conservative motif, recognized by proteinases of potato virus y, was inserted between nib and ppiv, which will release functional ppiv from the fused protein after infection by potato virus y. then, plant expression vector pnpa was constructed by ligating the fusing gene and pbi121, which is knocked out gus gene

    以馬鈴薯y病毒的復制酶（ nib ）基因為模板，通過聚合酶鏈式反應獲得nib基因，並在nib基因末端保留了在病毒基因組中nib與外殼蛋白（ cp ）基因相銜接的保守序列。
  6. A approximately 460bp dna fragment was amplified by pcr from lactococcus lactis nizo r5 genome. the primers used in this study comprised the following nucleotide sequences : 5 " - cgcgaattcgatataggtttattgagt - 3 " and 5 " - atgaagcttatccatgtcagaactaa - 3 ". conditions used for the pcr consisted of 30 cycles of 94 ? for0. 5min, 45 ? for imin and 72 ? for 1. 5min, plus one additional cycle of 72 for 10min

    根據已發表的乳鏈菌肽前體基因的dna序列，設計兩條引物並引入酶切位點。以lactococcuslactisr5基因組dna為模板， pcr反應條件： 94變性30s ， 45退火60s ， 72延伸90s ，反應進行30個循環。成功擴出一條約460bp的dna片段。
  7. This tutorial teaches you how to embed javamail in your geronimo server, link it to your application, and use it to easily send template - based e - mail through the velocity engine directly from your web application

    本教程向您展示如何在geronimo服務器中嵌入javamail ，將其鏈接到您的應用程序，以及將它用於直接從您的web應用程序通過velocity engine容易地發送基於模板的e - mail 。
  8. Using v2 & 5 and alkylamines ( cs - cao alkyl chain ) as precursor, vanadium oxide nanotubes which have an unique structure that alkylamines intercalate into layers of tubes wall affecting the layer spacing were prepared. their layers spacing ranges from 1. 25 nm to 3. 82 nm according to the length of alkyl chain. moreover, the growth mechanism of vanadium oxide nanotubes have been investigated and 3 - 2 - id model was established to interpret the vanadium oxide nanotubes growth process. potassium niobate is a functional materials which can be used as photochemical catalysts. lt is well known that the catalytic activites are affected greatly by the surface area of catalyst particles on which the reaction take place

    以系列烷基胺和五氧化二釩為原材料，通過簡單的水熱反應合成出了氧化釩納米管，這種納米管結構獨特，烷基胺作為模板劑內嵌入納米管管壁層間，成為支持納米管的骨架，並影響層間距大小，納米管管壁層間距隨著烷基胺碳鏈長度的不同在很大范圍內變化，通過採用不同碳鏈長度的烷基胺（ c _ nh _ （ 2n + 1 ） nh _ 23 n 20 ）作為模板，來控制氧化釩納米管的層間距，層間距可調控范圍從1 . 25nm到3 . 82nm 。
  9. A very professional patch tools that can automatically compare the difference between before and after the patch, can also be adjusted manually how subsidies can be byte - by - patch, and can also use ordinary template find two replacement ; patch before and after the file size may vary ; patches can be a single file, but also can be dealt with a number of different set, different directory, or even the name does not match the number of documents and links, such as text interface fully customizable ; can be saved by upgrading programme to use can use built - in and external compression ; or may not revise its own compressed form ; is completely free

    一款非常專業的補丁製作工具，可以自動比較補丁前後的差別，也可手工調整如何補貼；可以對位元組逐個補丁，也可以使用普通和模板兩種查找、替換；補丁前後的文件尺寸可以不同；可以對單個文件補丁，也可以處理多個不同盤、不同目錄、甚至名字並不匹配的多個文件；界面文字和鏈接等完全定製；可保存方案以備升級使用；可以使用內置和外部的壓縮器；也可以不壓縮自行修改窗體；完全免費！
  10. In e coli, dna polymerases are key enzymes involved in two distinguished pathways contributing to untargeted mutagenesis. replication of dna by pol v ( umuc ), in the presence of umud1, reca and single strand binding protein ( ssb ), is highly mutagenic and exhibits a predominant mutation pattern of base transversion. another error prone polymerase involved in untargeted mutagenesis is pol iv, encoded by dinb gene

    在umud ' ， reca和單鏈結合蛋白ssb的協助下， polv （ umuc ）能在單鏈模板上催化dna合成並產生高頻率的以堿基顛換為主要形式的突變；另一個與非定標性突變有關的易誤dna聚合酶是pol ，為dinb基因的編碼產物。
  11. A pair of primers were designed according to the published sequence of gnrh2 ' s gene mrna and transporter gene with oligo version 4. 1 softwarre, they were annealed by their 3 ' terminal brief complementary base sequence to form small segment double chain, therery, they serve mutually as template and primer, and their extension were carried out to synthesize 90 bp " gnrh / trs

    本研究根據genbank中已發表的人gnrh2基因mrna序列以及轉運肽（ transporter ， trs ）基因核苷酸序列，藉助oligo4 . 1設計了一對寡核苷酸引物，以引物3末端的短互補序列退火形成小段雙鏈，從而互為模板和引物，通過引導合成長達90bp的gnrh trs序列gnrh trs 。
  12. They inhibits the growth of fungi ( filamentous fungi especially ) while are non - toxic to plant cells. the main results were as follows : 1. obtaining of spcema ( signal peptide modified cema ) spcema ( 187bp ) was amplified with two long complementary primers ( p2 and p3 ) and two primers ( pl and p4 ) containing restriction enzyme recognition site

    帶信號肽cema基因的pcr合成以兩條部分重疊長鏈引物p _ 2和p _ 3延伸產物為模板， p _ 1和p _ 4為正、反引物進行pcr擴增，獲得了改造的抗菌肽基因spcema （ 187bp ） 。
  13. The paper, in the way of math morphology, manages to classify the linear elements, the same type but different width in the scanning, and result in the two - valued linear image in the same level. in the fine division of the target image, a way of math morphology based on the double structure of cell stencil is put forward, which prevents the terminals and the acnodes from losing and also reduces effectively time in doing so. as the result of the framework of the fine division, vector method is formed in which its track is monitored by using dynamic change of pace about freeman ' s chain code

    本文用數學形態學相關理論方法實現了對掃描圖像中具有同一線型但不同線寬的線狀要素進行分類，在同一層上得到同一線寬的二值線狀要素圖；在對此目標圖像進行細化時，提出了基於雙結構單元模板的數學形態學細化演算法，用該演算法對實際的線狀要素進行細化，避免了端點、孤立點等信息的丟失，且由於是并行處理，有效地提高細化速度；對于細化后的骨架線，提出了基於freeman鏈碼的動態改變步長保持精度跟蹤矢量化方法。
  14. Methods : a set of oligonucleotide primers were designed and used to amplify the vh and vl gene from anti - hbsag fab antibodies screened from phage antibody library. the products were cloned into puc19 vector and their sequences were analysed. the vh and vl gene fragments were tethered by a peptide linker and a leader sequence coding region, with the leader sequence added at 5 " terminus of each gene ( l - vh - linker - vl ) and designated as l - scfv

    方法以從噬菌體抗體庫中篩選獲得的抗hbsag的fab抗體基因為模板，分別擴增出其輕、重鏈可變區（ v _ l 、 v _ h ）基因，通過重組pcr方法將輕、重鏈可變區基因用連接肽（ gly _ 4ser ） _ 3的編碼序列連接，並引入前導肽編碼序列，構建具有l - v _ h - linker - v _ l結構的單鏈抗體基因。
  15. You ll want to avoid direct links between most pages in tapestry and instead access the " live " tapestry page, which only uses html files as templates

    如果在tapestry中想避免大多數頁面間的直接鏈接，可以訪問「即時的」 tapestry頁面，它只使用html文件作為模板。
  16. For the construction sector includes a review of updated environmental management information related to the latest trend in supply chain pressure in the construction sector, a set of user - friendly generic iso 14001 ems templates, and a user manual with sector specific practical examples for the construction sector to facilitate their adoption and implementation of the iso 14001 ems

    包括：與建造業供應鏈壓力的最新趨勢相關的新訂環境管理信息檢討簡易的iso 14001環境管理體系文件模板，以及載有建造業實例文件的使用手冊，以協助業界採用並實施iso 14001環境管理體系。
  17. A complete round of transcription involves the recruitment of polymerase and general transcription factors to the promoter, rna chain synthesis initiation and polymerase escape form the promoter, rna chain elongation, and finally termination with relaease of polymerase and nascent transcript from the dna template

    一個完整的轉錄循環包括ranp和通用轉錄因子被招募至啟動子、 ran鏈合成的起始和ranp從啟動子的脫逸、 rna鏈的延伸以及伴隨ranp和新生rna鏈從dna模板釋放的轉錄終止等過程。
  18. The ns5 protein of dengue virus is the largest molecule encoded by the virus genome with a molecule weight of 104 000. recent research work indicates that the ns5 protein acts as the rna - dependent rna polymerase ( rdrp ) in virus which has the ability to recognize and bind its template rna to synthesize a complementary strand

    近年來的研究表明， ns5蛋白具有rna依賴的rna聚合酶（ rdrp ）功能，即可以識別具有相對特異性的模板rna並與之結合，合成與模板互補的rna鏈，在病毒基因組復制過程中起關鍵作用。
  19. Secondly, we established a rdrp reaction system. then the recombinant ns5 protein was added to the system and its rdrp activity was confirmed after the newly synthesized rna showed resistant to rnase a. furthermore, we found that the recombinant ns5 could specifically bind antibodies in anti - den serum indicating the immunoreactivity of the recombinant ns5 and the irnmunogenicity of den ns5

    重組nss蛋白的rd即反應和反應產物的rnasea敏感性實驗表明，所得重組nss蛋白具有良好的rdrp活性，能以亞基因組rna為模板合成與之互補的rna ，新生鏈是與模板鏈相結合的雙鏈形式存在於rd即反應體系中。
  20. Curiously the exon ( 225 - 374bp ) of hsei is same with one of exons ( 1370 - 1519bp ) of sp17, but they use different transcription chain. high resolution stanford tng radiation hybrid panel was used to localize hsei and hseii in human chromosome

    同時很奇怪的是hsei的外元但25刁74b ）與sp （ spermautoantlgenicprotein ）基固的一個卜元廠70jgbp ）在基因組上處于同一位置上，只是它們使用了不同的模板鏈進行基因轉錄。
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