相片連測 的英文怎麼說

中文拼音 [xiāngpiānlián]
相片連測 英文
plate conjunction
  • : 相Ⅰ名詞1 (相貌; 外貌) looks; appearance 2 (坐、立等的姿態) bearing; posture 3 [物理學] (相位...
  • : 片構詞成分。
  • : Ⅰ動詞1 (連接) link; join; connect 2 (連累) involve (in trouble); implicate 3 [方言] (縫) ...
  • : 動詞1. (測量) survey; fathom; measure 2. (測度; 推測) conjecture; infer
  • 相片 : photograph; photoprint; photo; pix
  • 連測 : conjunction
  1. In this paper, first strand cdna of 3abc gene was synthesized using template rna extracted from cells infected with fmdv. the complete 3abc gene about isoobp was amplified by pcr and ligated into pgem - t easy vector. after transforming e. coli dh5 a, ampicillin resistant colonies were isolated and plasmid dna was prepared and analyzed by restriction analysis and pcr. presence of the full length 3abc gene was verified by nucleotide sequence analysis and the plasmid containing the expected sequence was named as pgem - 3abc. comparing the aquired sequence of 3abc with that of reference strains, the homology is more than 99 percent. the pgem - 3abc was digested with sal i and bgl ii and ligated into xho i and bgl ii - digested expression vector ptriex - 4 neo. lt was identified by restriction analysis and pcr and sequencing that this fragment had a 17bp deletion hi the nucleotide sequence 708bp of 3abc gene, which happened to form a terminator codon behind 3ab gene, but it contained the complete open reading frame ( orf ) of 3ab gene. positive clones were selected and induced with lmmol / l isopropyl - d - galactoside ( iptg ), bacteria were detected by sds - page and western blotting after properly treated. the results showed that the 3ab gene expressed successfully in e. coli and 33. 5ku fusion protein can be recognized by the positive bovine serum of fmdv. the amount of target protein is over 26 % of the total bacteria protein by gel thin layer scanning analysis

    擴增產物接到pgem - teasy載體中,轉化大腸桿菌dh5菌株,篩選氨芐青霉素抗性菌落,提取質粒經酶切鑒定、 pcr分析以及確證性序證明,所克隆的1500bp左右的段含有完整的3abc基因,與國外參考序列比,同源性在99以上。將重組質粒pgem - 3abc和表達載體ptriex - 4neo分別用sal和bgl與xho和bgl消化后,亞克隆3abc基因至原核表達載體ptriex - 4neo中,通過酶切鑒定、 pcr擴增以及序列分析,發現克隆到ptriex - 4neo載體上的段於3abc基因708bp處出現了17bp的缺失,碰巧在3ab基因后形成一終止密碼子,但3ab基因的閱讀框架完整,選出含有3ab基因完整閱讀框架的陽性克隆,用iptg誘導表達,收集菌液進行sds - page電泳、 westernblotting分析,結果表明, 3ab基因在大腸桿菌中成功表達,其表達產物為分子量33 . 5ku的融合蛋白,並能被口蹄疫病毒陽性血清識別。經薄層掃描分析,表達量占總蛋白量的26以上。
  2. Reclamation, purification and linkage of them respectively, then sequencing and analyses of according gene structure were made, results show that the complete sequence length of corresponding pcr product from brussel sprouts, kohlrabi and kale are 1665bp, 1650bp and 1650bp, containing the first two exons and introns and 22bp of the third exon

    對各pcr產物分別進行回收、純化、載體接和序列定及基因結構分析等,結果表明,該段在抱子甘藍、羽衣甘藍和球莖甘藍三種作物中的全長分別為1665bp 、 1650bp和1650bp ,包括應基因的前兩個外顯子和內含子以及第三個外顯子的22bp序列。
  3. Through cultivating five cold - season turfgrass ( lolium perenne, agrostis stolonifera, festuca rubra, festuca arundinacea, bromus inermis ) in basin, their drought to lerance indexes, including the planting height, the root growth, the relative water content of leaves, the penetration of membrane, were comprehensively evaluated to compare their drought tolerance

    摘要採用盆栽育苗法,在5種冷季型草坪草苗期續乾旱脅迫下定植株高度,根系生長,葉對含水量和質膜透性等抗旱指標,以綜合評價5種冷季型草坪草的抗旱性能。
  4. Furthermore, the current research about body measuring and modeling is just for costume and military affairs, and pay more attention to the head dimension and shape. with the development of human nature during the manufacturing, body cad model is widely applied in industry design, ergonomics, engineering design, humanics research and iatrology research. the body cad model also can be the basic data for the design of respirator

    本文使用nurbs曲面直接擬合的方法對量的點雲進行曲面重構,將系統的優化方法應用到nurbs曲面重構中,利用插值曲線對量點雲進行分塊處理,解決用nurbs曲面擬合中曲面的光順與曲面與點雲的誤差之間的矛盾問題,使反求模型中各曲面之間接、光順過渡且能夠反映出人體頭部的細部特徵。
  5. In order to check if it is the aim gene, we devised pcr with a new pair of primer, sequenced and registered the product with registration number : af449446. moreover we forecast and analysis the primary, secondary, tertiary and quaternary structure of the three protein : osftszi, crftszi and crftsz2 which has already cloned by our team before. after that we construct ftsz molecular evolution tree to site them in

    又將生物信息學技術同實驗技術結合,針對ftsz保守區設計引物擴增出一條衣藻ftsz段,進行est搜索、比對、拼接,最終克隆出新基因crftsz1 ;同本試驗室曾經獲得的另一個衣藻crftsz2基因進行蛋白質的一、二、三、四級結構預、分析及比較尋找進化線索,建立了ftsz蛋白的氨基酸進化樹作進一步的進化定位。
  6. Sequence analysis showed that, this fragment has a homology of 99 % to the previously reported choe from rhodococcus equi. after cloning and subcloning and three identical fragments were obtained from three independent pcr, lacking three continual bases ( ttc, encoding the pheamino acid ) compared with choe, thus it can be assumed that the new fragment, designated as choew, and choe belong to the same gene family, even it might be the natural mutation of choe

    段進行克隆、亞克隆之後序分析,發現與已克隆的來源於馬紅球菌的膽固醇氧化酶基因cboe有99的同源性;並且三次獨立的pcr均得到同的段,所克隆的基因序列與choe比,續缺失三個堿基( ttc ) ,即應的氨基酸序列缺失一個氨基酸( phe ) ,因此判斷所克隆的基因段與choe屬同一基因家族或原有基因的天然突變體,命名為choew 。
  7. We sequence the inserted gene fragment of the indentified recombinant clone. the result is : angiostatin gene orf ( open reading frame ) links with the orf in expression vector correctly. but the first base of the codon aaa coding for lys414 in plg kringle 4 domain mutates from a to g which leads lys change to glu

    隨后取通過上述鑒定的重組克隆菌,對重組子插入序,結果為: as基因開放讀碼框與表達載體的讀碼框正確匹配,但在其kringle4區當于編碼plg的lys ~ ( 414 )密碼子aaa的第一位堿基由a突變為g ,導致應的氨基酸殘基突變為glu 。
  8. There are also the power - on circuit for gsm module, indication circuit, the uart to pc, etc. the mcu program, written with c51 language, include gps position, alarm of dilapidation, asynchronous communication and sms, clock management, etc. after development, the mts " capability had been tested

    另外還包括gsm的開機電路,指示電路,與pc接的串口等等。單機軟體選擇了c51語言進行設計,包括gps觀、崩塌傳感器報警、異步通信和短消息、時鐘管理等模塊。在完成終端的研製后,對儀器的性能進行了檢
  9. The technical breakthroughs in growth of nd : cngg had been made. in particular, continuous laser operation was achieved from nd : cngg pumped by ld. when the crystal wafer was end - pumped by one bar of ld with 807nm wavelength, the cw laser output power of 123. 1 mw was obtained with slope efficiency of 22. 3 %

    本論文用自動化熔體提拉技術成功生長出< 111 >方向的直徑25mm以上,長度80mm以上的平界面無核心nd : cngg單晶,確定了晶體結構和物量了晶體的光譜性能,晶體消光比達到34db ,晶體生長技術有新的突破,實現了續激光運轉,用單支807nm半導體激光二極體端面泵浦該晶體子,在國內首次獲得123 . 1mw的1 . 062 m續激光輸出,斜效率達22 . 3 % 。
  10. Moreover, video control program to implement internal function of fpga is designed including video capture time sequence control, ping - pang frame buffer read and write time sequence control and lcd display time sequence control, and program ' s simulation and analysis is also provided. at last, this paper presents a portable iv ' s video processing system, and proposes three buffer strategy to control capture buffer. and a moving object detection algorithm of combing an adaptive background subtraction technique with a three - frame differencing is adopted

    設計了基於fpga系統結構的車載視頻顯示電路板;利用單機io口模擬i2c時序,實現了視頻解碼晶元控制;利用fpga實現視頻控制,研究了採集通道時序控制、雙幀存ram讀寫時序控制及lcd顯示時序控制的方法,並進行了軟體模擬和分析;設計了車載視頻檢系統方案,給出了管理採集緩沖區的三幀緩沖策略,採用綜合三幀差分和自適應背景減的演算法實現運動檢通體檢去除虛目標,模擬實驗證明其有效性,同時分析了該演算法在dsp視頻檢系統中的簡單實現方法。
  11. The early studies are mostly focused on the method of gluing piezoceramics on structural surfaces, which has some disadvantages such as difficulties to protect the ceramics and the connection wires, bad coupling with only one surface glued on the base materials, low signal - to - noise ratio etc. these problems can be solved using the embedded piezoceramics, and furthermore, the piezoceramics can be placed in the optimal positions, especially in the optimal deepness for the piezo - actuators, according to an optimization algorithm befor e they are embedded, so the actuator effects and sensor signals are thereby enhanced

    早期的研究主要集中在表面粘貼壓電的結構,表面粘貼壓電具有一些無法克服的缺點。本文著重進行利用埋入復合材料結構的壓電傳感器和壓電驅動器對其振動進行主動控制的關理論和實驗研究,並介紹其應結果。埋入型壓電材料的優點主要是能保護壓電傳感器和作動器及其線、增強壓電材料和基體材料的耦合、優化埋入壓電陶瓷的深度和厚度可增強壓電傳感器的量信號並提高信噪比等。
  12. For the first time, the complete long env gene of the jaagsiekte sheep retrovirus ( jsrv ) has been colpned from provimses in china in sheep genome and sequeneed, the gene is 1836 nucleotides long. there are 12 nucleotides mutations compared with type i and type ii jsrv counterparts the sequences of the virus was 87 % to 88 % identical to the described three jsrv env sequences

    將pcr產物純化,並與puem - t載體,轉化大腸桿菌,經pcr ,酶切鑒定及序列定,得知所得env段與型jsrv同源性為88 ,與型jsrv同源性為87 ,證明所克隆基因為外源性目的基因,至此,我們在國內首次獲得了env陽性克隆。
  13. Based on the practical measurement data that had gained on the equipment of continuous solid - state polycondensation, which has the output for pet industrial yam 10 kt / a, studies into influences of reaction temperature, residence time, purity and flow rate of circulating nitrogen on the reaction of solid - state polycondensation, discusses the production process of continuous solid - state polycondensation for terylene industrial yarn in detail

    摘要以已投產的年產萬噸級續固縮聚裝置生產工業絲級滌綸增黏切的反應條件為依據,從原料切、反應溫度、停留時間、循環氮氣純度及流量等因素對固縮聚反應的影響,詳細地對續固縮聚生產工業絲級滌綸增黏切的生產工藝加以探討。
  14. Sequences flanking tn5 - 1063a can be recovered from the genome of mutant by excision, self - ligation and transfer to e. coli. the total dna of mutant was excised with ecori, which cut the genome frequently but not cut the transposon. after sequencing the self - ligated transpon, dna fragment flanking tn5 was obtained. the result showed 042bm - x1 contains a tn5 insertion in the gene smc00190, which function was unknown and was demonstrated to be related to salt tolerance by this study, and the gene was named as rst - 0x1

    通過ecori酶切突變株基因組,得到完整的tn5 (含有在大腸桿菌中起始復制的oriv )及其側翼的序列段,該段自后轉化大腸桿菌,以tn5兩端已知的序列設計引物進行序。 blast的分析序結果表明, 042bm - x1和042bm - x2中tn5分別定位在苜蓿中華根瘤菌1021染色體上smc02682和smc00419基因內部,本實驗證明它們和042bm耐鹽關,命名為rst - 0x1和rst - 0x2基因。
  15. And the two pah ' s of pcr primers that bind to the adapter and the sequence of f fragment close by tn5 respectively were also designed. the genomic dna of b8 was isolated, digested with bamh i, and ligated to the adapter. using the two pairs of the primers, two rounds of pcr were performed hi turn and a fragment of 239bp was amplified successfully. lt was proved by cloning and sequencing that 18bp of the fragment is the sequence opposite to f fragment on the left of tn5 insertion site in b8f, the other is part of the 728 bp of f fragment. this result makes it possible to continue to carry out chromosome walking, to clone and sequence the whole genes of b fragment and f fragment, and to reveal the antagonistic molecular mechanism of b8

    試驗研究設計併合成了由40和44個堿基的寡聚脫氧核苷酸組成的染色體爬行接頭,在接頭序列和定的f段近tn5的序列上,設計了2對染色體爬行用的pcr引物,從b8菌株中提取基因組dna , bamhi酶切,與染色體爬行接頭接,依次用2對引物進行pcr ,擴增出239bp產物,經克隆、序,發現其中18bp為擴增的應于f段在b8f菌株tn5插入位點對面的序列,其餘則為f段728bp序列的一部分,為進一步進行染色體爬行,克隆和定整個b和f基因,揭示陽菌株的拮抗分子機制提供了技術資料貯備。
  16. The dimensions of this hybrid mechanism is " from the result of the example in chapter 4. a rotary encoder is used to gather the position signal of the crank, according to which micro - computer control the rotation of the setup motor assembled with the other side link in order to adjust the position of this side link. only if we turn arbitrarily the crank connected to the rotary encoder, a given path is generated precisely

    根據第四章中優化綜合得出的結果,製作五桿機構模型,採用一角度傳感器得作主運動的曲柄的位置參數,由單機根據此參數來控制與另一曲柄的步進電機的轉動,使桿點精確再現給定的軌跡。
  17. The upper computer that connected with modem via rs - 232, and the modem connected with the public telephone network in the monitoring center communicated with the distant controller

    上位機通過rs - 232與modem接入公用電話網,實現對單機控制器的遙、遙控。
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