篩析結果 的英文怎麼說

中文拼音 [shāixījiēguǒ]
篩析結果 英文
sieving result
  • 篩 : 名詞[書面語] （植物名） sedge
  • 析 : Ⅰ動詞1. （分開; 散開） divide; separate 2. （分析） analyse; dissect; resolve Ⅱ名詞（姓氏） a surname
  • 結 : 結動詞（長出果實或種子） bear （fruit）; form （seed）
  • 果 : Ⅰ名詞1 （果子） fruit 2 （事情的結局; 結果） result ; consequence 3 （姓氏） a surname Ⅱ動詞（吃...
  • 結果 : 結果bear fruit; fruit
  1. As a consequence of the results of the aforementioned analyses, patients referring pain located at the right epigastrium were selected and further evaluated

    基於前述分析之結果，病患稱右上腹部疼痛的，我們會加以篩選，再進一步評估。
  2. 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

    擴增產物連接到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分析以及確證性測序證明，所克隆的1500bp左右的片段含有完整的3abc基因，與國外參考序列相比，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載體上的片段於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。
  3. An american cost ealuation from the iewpoint of the outcome of pyelonephritis concluded that a single screening culture in the first trimester was cost - effectie if the prealence of bacteriuria was 12 % and the risk of pyelonephritis in bacteriuric women was 113 % [ 69 ]

    美國從腎盂腎炎的結果進行效價分析，認為在開始的三個月中一次篩選培養最有效的，如果菌尿患病率為12 %那麼帶菌尿的婦女中患腎盂腎炎的風險是113 % 。
  4. The results are obtained as follows : we analyze the features of kinematics and dynamic of the crusher. the improvement on the crusher structure design is made in the following aspects : involutes beat board, adjust mechanism on the back protect board and sieve plate, distributaries system, sieve plat, crusher space, rotor, hammer. furthermore, strength check is carried out

    通過本題研究取得了以下研究成果：對破碎機進行了運動和動力學分析，結構優化改進，包括：漸開線反擊板設計，后側護板和篩板的恆力調節機構設計；分流系統的設計；篩板的設計；破碎腔的設計；轉子的設計；錘頭的設計。
  5. At first, 1. 67 u g per well mcab all was coated on three wells of a plate, and then 1. 5 x 1011 phage virion was diluted and added, after incubating with the target, wash away unbound phage by tbst ( 0. 1 % tween - 20 ), the bound phage was eluted with ph 2. 2 tris - gly buffer and amplified, the specially bound phage was enriched by taking through addition binding / amplification cycles. ln the following cycles, the stringency of panning can be increased by raising the concentration of tbst or decreasing that of mcab all, collecting and titering the washing phage of last time and output phage in each round, the selective ratio and the false positive rate of each round were worked out, the gradually increasing of selective ratio and decreasing of positive rate shows that the panning was effective. after 4 rounds of panning, 11 phage clones were selected after competitive - ellsa, the dna samples of 8 positive clones and 1 negative clone were sequenced and all the foreign peptides inserted was also deduced, a clear consensus binding sequence emerged

    在本實驗中，利用隨機12肽庫對抗豬瘟病毒（ classicalswinefeverviruscsfv ）糖蛋白me2的單抗a11進行表位篩選，經過四輪篩選以後，隨機挑取11個克隆作競爭- elisa檢測，結果表明，所挑11個克隆中，有9個克隆能對me2蛋白和a11反應產生抑制作用，抑制率最高可達64 ； dna測序以後經過dnastar軟體分析，發現它們的核心序列為anwralsl ，該核心序列與豬瘟病毒e2蛋白的28 - 35位氨基酸ttwkeysh具有同源性；夾心- elisa檢測和western - blotting試驗均證明所挑陽性克隆能被a11所識別；人工合成含核心序列的多肽經間接elisa試驗證實，也能被a11識別。
  6. In order to analyze their psychological characteristics comprehensively, the research was carried out on 152 bearing and unboarding children in wenzhou, which adopt group intelligence test for students, eysenck personality questionnaire ( epq ), group thematic test for students ( t - tat ) and symptom checklist 90 ( scl - 90 ). it is shown that these children has developed their unique characteristics

    為了全面了解寄託兒童的心理特點，本研究採用中小學團體智力篩選測驗、艾森克人格問卷（兒童版） 、學生團體主題統覺測驗（ g ? tat ）和癥狀自評量表（ scl ? 90 ）四個量表對溫州市152名寄託兒童和一般兒童進行調查分析，結果表明，寄託兒童已經形成了自己的特徵。
  7. The simulation on synthetic data is made and the result is discussed. 5 ) by using borland c + + builder and matlab, a semi system, i _ miner, is developed to mine association rule. it can realize other functions just as data cleaning, data transform, etc. furthermore, i _ miner is applied to an actual industry database

    提出用趨勢變換序列dtw距離做篩選的搜索方法，有效提高整個搜索效率，並在模擬數據庫上進行模擬實驗，並對實驗結果進行分析和討論； 5 ）以borlandc + + builder和matlab為開發平臺，設計一個進行關聯規則挖掘的準系統i _ miner ，可以實現數據預處理，數據變換和關聯規則挖掘等工作。
  8. This paper analyzed the mechanism that gas and liquid flow through the holes according to the fluid characteristics of the compound tray, and put forward that there are three states of liquid flowing, gas flowing and blocked for the holes because of the foam fluctuating on the tray while the compound tray operates

    本文根據復合塔板的氣液流動特點，分析了氣液穿孔流動的機理。根據前人的研究結果，提出復合塔板在操作時，由於泡沫層的波動，其篩孔存在通氣、通液和阻塞三種狀態。
  9. Powders properties of different phases such as the granularity, the shape and the component have been analyzed by the methods of sieving, gravity sedimentation, spectrophotometry, scan electronic microscope ( sem ), transmission electronic microscope ( tem ) and x - ray diffraction ( xrd ). the results show that technic of ball milling and parameters of heat treatments are important influencing factors to properties of cu - zn powders

    採用篩分法、重力沉降法、分光光度法、掃描電鏡法、透射電鏡法和x射線衍射法對不同階段的銅鋅粉末的粒度、形貌、成分等性質進行了分析，結果表明：球磨工藝及熱處理參數對銅鋅粉的性能有重要影響。
  10. Grindability is determined by comparing the results of the screening analysis of the material sample to the calibration line

    通過把對磨后的樣品的篩析結果和校驗直線相比較來確定該物料能否被碾磨。
  11. Thus mechanical properties, heat resistance properties and solvent resistance properties of pu are greatly enhanced. crystal forms of composite materials, surfacial reactivity and adsorption assemble properties of zeolite are discussed in this paper by means of xrd, ftir and tg etc. the test results of xrd prove that mmt can be exfoliated into nanocomposites in pu / mmt, while zeolite keep its original crystal structure in pu / zeolite. the spectras of ftir prove that tdi can graft on the surface of the zeolite

    Xrd測試結果證實了有機蒙脫土在聚氨酷體系中能夠剝離成納米粒子，而聚氨醋/沸石分子篩復合材料中分子篩仍保持原來的晶型結構; ftir譜圖驗證了異氰酸酷（ tdi ）可太原理工大學碩士學位論文摘要與沸石分子篩表面的硅經基進行接枝反應形成穩定的化學鍵;而tg分析結果則進一步證實了分子篩的穿孔機理。
  12. The recombinant fasl - ecd was purified and its biological activity was analyzed on several cell lines and the most sensitive cell lines are selected. ( 2 ) using a computer program, a single short peptide is derived from antisense homology box of fas ligand and is chemically synthesized. ( 3 ) examine the apoptosis - inducing effect of the recombinant fasl - ecd and the ten - peptide on the most sensitive cell lines, and the relationship between them was analysed

    純化重組蛋白fasl - ecd ，並分析其生物學活性，篩選出對之最敏感的腫瘤細胞株； （ 2 ）根據生物信息學軟體分析結果，選取fasl胞外區256 - 265的十肽（ n ） - hlyvnvsels - （ c ）作為目標分子，委託生物公司合成該十肽； （ 3 ）分析fasl - ecd和十肽對最敏感腫瘤細胞的毒性作用，分析重組fasl一ecd及十膚作用的相關性。
  13. Analysis on the result of two diseases test among the newborn in penglai city from 1999 to

    2005年蓬萊市新生兒兩病篩查結果分析
  14. The results given by the improved software are not both statistically and biologically different from manually specified results, and thus can be used as an effective alternative for the latter. it has a very high sensitivity in determining cells with a tail, meeting the needs of screening tests. it has both a high sensitivity and a high specificity in determining cells with 2 damage grade, indicating a potentially good laboratory index

    結論彗星試驗圖像分析軟體經改進后，分析準確性得到提高，程序魯棒性增強，而且易用性改善，並增加了由操作者進行必要校正的功能;所得分析結果與人為指定的分析結果相比，並不同時存在統計學顯著差異和生物學顯著差異，可作為真實可靠的彗星數據分析系統應用;改進后的系統在拖尾細胞判定上具有很高靈敏度，可用於篩查試驗項目;在2級及2級以上損傷細胞的判定上同時具有較高的靈敏度和特異度，是實驗室研究中的優良指標。
  15. The work on physical mapping of the chromosome of s. nanchangensis ns3226 was initiated. nearly a full set of chromosomal asei - bamhi fragments of s. nanchangensis ns3226 were cloned and used as probe to hybridized against its genomic library. thirty four asei linking cosmids were observed from 162 hybridizing cosmids and 20 of them showed no obvious overlapping each other by bamhi digestion, suggesting distinct identifications

    此外，還開展了南昌鏈黴菌ns3226染色體物理圖譜構建的前期研究工作：基本克隆到了南昌鏈黴菌ns3226染色體上全套的ase - bamh片段，以它們為探針從南昌鏈黴菌ns3226的基因文庫中釣到164個陽性克隆，並從中篩選到34個ase linkingcosmids ，用bamh進行初步的酶譜分析，結果表明其中有20個cosmids的bamh酶譜相互間沒有明顯的重疊性。
  16. To determine that the integration of foreign genes had occurred hi the chloroplast genome at the directed site by homologous recombiantion and to evaluate the degree of homogeneity of the c. reinhardtii transformants, pcr and pcr - southern blot analysis were performed using the primers of c. reinhardtii chloroplast homologous fragment

    並根據衣藻葉綠體同源片段chll基因，設計一對引物對其葉綠體dna進行的pcr和southernblot分析。結果表明外源基因已經定點整合入衣藻葉綠體基因組的chll基因中，並且經過三輪抗生素篩選所得的衣藻葉綠體轉化子中，轉基因型葉綠體基因組拷貝佔多數。
  17. In this study, pichia pastoris system had been utilized for expression of fmdv 2c3abc gene which aimed for establishing a sensitive and specific molecular dignosis method. first, 2c and 3abc genes were amplified individually from p2 and 3abc postive clones and ligated together using pcr method, then this 2c3abc product was cloned into pgem - t easy vector and transformed e. coli dh5a competent cell. a postive recombinant plasmid which contained whole 2c3abc gene had been confirmed by pcr, enzyme digestion and sequencing. after that, the 2c3abc gene was sub - cloned into ppiczaa expression vector and transformed e. coli dh5 a competent cell and selected by zeocin ? antibiotic. the postive recombinant expression vector was linerized and electro - transformed pichia pastoris smd1168 competent cell. a recombinant pichia pastoris had been obtained by zeocin ? antibiotics selection and induced with 0. 5 % methanol for target protein expression. the expression product was analysised by sds - page and western blotting assay. the result sh owed that 2c3abc gene was expressed successfully in pichia pastoris and the product was a 95ku fusion protein which could be recognized by anti - fmdv serum. the amount of target protein was over 15 % of the total bacteria protein by gel thin layer scanning analysis. this research had supplied materials for establishing a fmd diagnosis method to differentiate infected animals from vaccinated animals

    首先，用p2和3abc陽性克隆通過連接pcr方法獲得目的基因並將其克隆到pgem - teasy載體上，並轉化e colidh5a感受態細胞中，經pcr 、酶切以及測序證明得到了完整的2c3abc基因，並與國內外參考序列進行比較分析。然後，將目的基因亞克隆于ppiczaa表達載體並轉化大腸桿菌dh5a ，以zeocin ~ （ tm ）抗性篩選陽性克隆，大量提取重組表達質粒並用pme酶線性化后電轉化入畢赤酵母smd1168感受態細胞，通過zeocin ~ （ tm ）抗生素梯度濃度篩選，獲得重組酵母用0 . 5甲醇誘導表達，通過sds - page電泳、 westernblotting分析，結果表明， 2c3abc基因在畢赤酵母中成功表達，其表達產物為一95ku的融合蛋白，並能被口蹄疫病毒陽性血清識別。
  18. The appropriate technology was chosen and identified from some various preparation technologies

    根據分析結果，從不同的膜制備工藝中初步篩選出了合適工藝。
  19. Analysis of the prevalence of human papillomavirus infection in the lower genital tract of 2285 women

    2285例女性下生殖道人乳頭狀瘤病毒感染篩查結果分析
  20. A screening survey of diabetes mellitus in 5 000 peasants of bai nationality in dali autonomous region of yunnan

    雲南大理白族5 000農民糖尿病篩查結果分析
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