載模板 的英文怎麼說

中文拼音 [zǎibǎn]
載模板 英文
adaptor plate
  • : 載Ⅰ名詞(年) year : 一年半載 six to twelve months; six months to a year; 三年五載 three to five ...
  • : 模名詞1. (模子) mould; pattern; matrix 2. (姓氏) a surname
  • : 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) ...
  • 模板 : [土] formwork; mould; shuttering; follow board; form board; match board; match plate; mother plat...
  1. In this study, iltv - nm98a strain and iltv - wanggang strain were multiplied in chorioallantois. a pair of primers were devised according to the nucleic acid sequence of iltv tk gene and the dna of multiplied virus was used as pattern to amplify the gene of tk by polymerase chain reaction ( pcr ). the product of pcr was linked with suitable plasmid. then, the recombined plasmid was converted to escherichia coli. the converted escherichia coli

    根據已發表的iltvtk基因的核苷酸序列設計一對pcr引物,以增殖的兩株iltv的dna為,分別對它們的tk基因進行pcr擴增。將回收的pcr產物連接到適當的質粒體上,轉化感受態大腸桿菌,通過篩選對iltvtk基因的陽性克隆進行擴增培養。
  2. 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,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體pmd - 18 - t上,篩選反向克隆,然後將其反向構建到植物表達體pbinyxw的camv35s啟動子和tmv增強子「 」的下游,構建成反義表達體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。
  3. This time, using cdna of zmcdc5 as template, we amplify a sequence by means of pcr technology. and then, using restrict endoenzyme and ligase, we conjunct the 0. 8kb length dna sequence in a expression vector, pet - 30a. after induction, expression and purification, we obtained a 35. 4kda truncated fusing zmcdc5 protein which contains 267aa ( 647 to 914aa in zmcdc5 ). with the purified protein, we got its antibody and testified the antibody by means of western blotting and dot blotting

    本實驗是以zmcdc5的cdna為,使用pcr獲得基因片段,再通過酶切連接,將得到的0 . 8kb的基因片段構建於pet - 30a表達體上,經過誘導表達和純化,獲得zmcdc5的融合蛋白,其中包括了zmcdc5925個氨基酸中647 914共267個氨基酸殘基
  4. When i download user template and finger print, can i save it in a file like csv format

    使用者和指紋時,我能否如csv格式保存到文檔?
  5. The paper is based on innumerable practical heavy - load road data, deliberate heavy - load standard in detail through theoretical arithmetic, and bring heavy - load standard about cement concrete pavement and asphalt concrete pavement separately ; in the meantime, through a large quantity of cement concrete pavement stress calculation, the paper puts forward relation expression between load on concrete board and stress level under board ; meanwhile, the paper puts forward traffic classification about cement concrete pavement and asphalt concrete pavement ; through bearing board testing on each structure sheaf the paper finds the material modulus gets modified ; through comparing position equivalent rebound modulus to theoretical equivalent rebound modulus, the paper points out limitation of nomograph in course of cement concrete pavement design, whereby, puts forward modifier formulas about theoretical equivalent modulus

    本文以大量的重道路資料為主,從實際出發,結合理論計算,對重標準進行了詳細的討論,分別給出了水泥混凝土路面與瀝青混凝土路面的重標準了;同時,通過大量的水泥混凝土底應力計算,推導出了混凝土面底應力水平的關系式;給出了水泥混凝土路面與瀝青混凝土路面的交通分級;通過對試驗路各結構層進行承測試,發現現有材料量較以前有了明顯的提高;對比現場實測的當量回彈量與理論當量回彈量,指出現有水泥路面設計中的諾謨圖不能完全符合現有道路材料,從而提出了對理論量的修正公式。
  6. 2. obtaining of mcema ( modified cema ) and plant defensin afp gene mcema ( 141bp ) was amplified with pucspcema plasmid as template and p5, p4 as primers, and plant expression vector pemcema was constructed

    Mcema和植物防禦素基因的pcr合成以經測序驗證的spcema為,用p _ 5和p _ 4擴增得到了全長141bp的mcema ,並構建了植物表達體pemcema 。
  7. It has been reported that the eiav s2 is not essential and does not appear to affect virus infection and replication in vitro. thus, we introduced a his - tag into the s2 gene of an eiav infectious molecular clone recombinant plasmid ( pok8266 ) by using soe pcr method and obtained a new recombinant plasmid with his - tag, designated as eiav - pok8. 2 - his

    本研究應用已構建好的eiav驢白細胞弱毒疫苗株的感染性分子克隆體( pok8266 )為,通過soepcr方法在感染性分子克隆體的s2基因獨特區內引入突變點,形成含有酶切位點( nspv )的突變體( p1p4 ) 。
  8. Secondly, the hyaluronate lyase gene ( hyl ) was cloned into the vector puc19 by pcr using the total ona sample ofs. equi as template and partially sequenced, too

    Equi的總dna為,通過pcr方法,克隆了透明質酸分解酶基因( hyl ) ,測序后連接到表達體pse380的trc啟動子下游,構建表達質粒pse380 - hyl 。
  9. Provides html tutorials, web design articles, free templates, tools and webmaster resources

    -提供矢量圖庫psd網頁flash源代碼等素材下
  10. Firstly, for the system of moulding board and support frame in construction the side pressure and screws are analyzed. the material and structure form of support frame are discussed. the design of support frame uses the method of limited state, and also it analyses the integer stability, part stability, and single stability, and then proposes the load analysis of multi - level support frame

    首先,針對轉換層梁體系及支撐架施工,重點分析了轉換層結構現澆混凝土對側壓力值及對拉螺桿的計算;討論了轉換層支撐體系的形式及構造,詳細論述了基於極限狀態設計的支撐架計算方法,包括縱橫向水平桿的強度驗算、立桿的整體穩定性、局部穩定性、單肢桿件穩定性等驗算,並提出了多層支撐架的施工荷計算方法。
  11. Clone human wnk4 full length cdna into pgem - t vector human kidney total una was extracted and used as template to amplify wnk4 full length cdna with the forward primer ( 7 - 27 ) and reverse primer ( 3808 - 3833 ) with the long template expanded pcr system kit

    5 .原位雜交以小鼠腎臟總翩a為,擴增wnki基因外顯子1 , 24一28 ,以a片段和wnk4基因外顯子13一16片段,純化后連接在pgem一t體上。
  12. Constructing cdna expressing library of erythrocytic plasmodium falciparum from hainan : the total rna was obtained by using. triplix kit. a modified oligo ( dt ) primer ( cds ffi pcr primer ) was used in the single - stranded ( ss ) dna synthesis reaction. the ss - dna was reversely transcripted from total rna. double - stranded ( ds ) cdna was amplified by long - distance ( ld ) pcrafter the digestion with proteinase k and sfi i, the cdna with no less than 200bp was collected and purified by glass - milk kitthe library was constructed after the ligation of cdna to tiplex2 phage particle packaged with the packaging extract system in vitro. a high titer and high recombinant ratio of cdna library was constructed

    構建惡性瘧原蟲海南株紅內期cdna表達文庫提取紅內期惡性瘧原蟲海南株總rna ,直接以總rna為使用cdna文庫構建試劑盒,首先反轉錄合成ss一dna ,再擴增合成ds一dna ( cdna ) ,對擴增產物用蛋白酶k消化及左z丁i酶切,抽提蛋白、去除rna后,用玻璃奶試劑盒純化、回收20obp以上的片斷,經與體連接再用蛋白包裝物包裝后形成未擴增文庫,最後擴增完成惡性瘧原蟲海南株紅內期cdna表達文庫的構建。
  13. Other chromosome elements, telomere and ars, have also been cloned for constructing artificial chromosome. arabidopsis telomere was cloned from pcr products using telomere repeat primers without other template. a 2000bp fragment of ars was released from arabidopsis genomic bac clone t14a4 by claidigestion and subcloned into clai digested pbluescript

    擬南芥的端粒是利用端粒的重復序列進行無的pcr擴增得到的;約2000bp的ars片段是從擬南芥的bac克隆t14a4中用限制性內切酶c1a1切下,然後亞克隆到通用體pbluescript上。
  14. The full length cdnas of 17 - hsd1 and 17 - hsd3, 17 - hsd8 were obtained by library screening and race, respectively. expression patterns ( tissue distribution ) of three types 17 - hsds were checked by rt - pcr and northern blot. the recombinant constructs of 17 - hsdl / pet blue2 and 17 - hsd8 / pcdna 3. 1 were made and subsequently transformed into the corresponding host expression cell of ( de3 ) placi and mammalian hek 293 cell

    首先從genebank下在其他脊椎動物中已被克隆17 - hsd1 , 17 - hsd3的氨基酸和核甘酸序列,並在序列保守區域設計簡並引物,然後分別以羅非魚卵巢和精巢cdna為進行rt - pcr擴增得到17 - hsd1 , 17 - hsd3的中間片段。
  15. Using cad technique, the author developed airborne, shipborne and trunk - mounted structural designing templates, created structural designing data base of airborne, shipborne and trunk - mounted electronic equipments and realized the parameterizing modular design. the typical experiment of a project indicated that the cad structural designing system is practical and it has been playing an important role in the structural design in the project

    文中利用cad技術開發了機、艦、車三種結構設計,編制了機、艦、車電子設備結構設計資料庫,並實現了機櫃參數化塊設計,通過某項目設計定型試驗表明,本cad結構設計系統是實用的,並在某項目的結構設計中發揮了重要作用。
  16. The assembly is not called if the template is loaded from the startup directory of word

    如果從word的startup目錄加載模板,則不會調用該程序集。
  17. More office downloads, templates, and clip art

    更多的office下和剪貼畫
  18. More office downloads, templates, and clip art top of page

    更多的office下和剪貼畫
  19. Newsgroups for office users more office downloads, templates, and clip art

    更多的office下和剪貼畫
  20. More office downloads, templates, and clip art tips and tricks for powerpoint 2000

    更多的office下和剪貼畫
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