清篩 的英文怎麼說

中文拼音 [qīngshāi]
清篩 英文
cloth cleaning
  • 清 : Ⅰ形容詞1 （純凈） unmixed; clear 2 （寂靜） quiet 3 （清楚） distinct; clarified 4 （一點不留） w...
  • 篩 : 名詞[書面語] （植物名） sedge
  1. We screened the resulting e. coli samples using blood serum from a person ( me

    的血清，來篩檢大腸桿菌產生的蛋白質樣本。
  2. Bx - glass washing machine ( water machine ), is the broken glass cleaning indispensable equipment, the structure is simple, reliable operation, the glass was used extensively

    Bx型玻璃清洗機（水篩機） ，是國內碎玻璃清洗不可缺少的設備，具有結構簡單，運行可靠，被各玻璃廠廣泛採用。
  3. The target gene was then subcloned into plasmid vector and induced by iptg for its expression. after that, the recombinant protein was purified and used for the identification and characterization of its immunogenicity. the effect of the induced specific ige antibody on the hepatic granuloma formation and fibrosis after challenge infection with schistosome cercariae was evaluated

    Niptg誘導表達，產物沉澱中於約45kda處顯見高合蛋白表達帶， westernblot分析表明，該蛋白帶可被篩庫血清中特異性lge抗體識別；而載體本身表達的26gst蛋白帶則否。
  4. Whole machine with simply structure, crush room and material feeder for easy clean and dismantle. the touching parts of material, all adopt stainless steel, to acid endurable, erosion endurable. the machine with balance operation, low noise, good effects on crush and low energy consumption

    本機有加料機構及粉碎機構組成，結構簡單，清洗方便，與物料接觸部分全部採用不銹鋼製造，能耐酸、堿侵蝕、噪音低、效果好、能耗低、粉碎刀片可四面更換，並可根據物料的不同性能及粗細通過更換篩網布獲得理想的效果。
  5. Experiment shows that the antigen extracted by autoclave is best for dot - ppa - elisa. applying the x2 test, optimal concentration of antigen was determined, and the optimum dilution of enzyme hrp - spa was 1 : 10. the high specificity of dot - ppa - elisa was proved by the specific blocking test, and also by the cross - reaction test in which the diaphragm does not react with the antibodies against salmonellosis, pasteurellosis, chlamydiosis, hcv, ppv, brucellosis, erysipelas suis, colibacillosis, prv

    試驗中對多種方法提取的診斷抗原進行了比較、篩選；確定了dot - ppa - elisa的最佳工作條件；測定了st - 171株的免疫豬血清抗體及c群、 2型人工感染豬血清抗體效價，並初步確定了該方法的陽性標準。
  6. 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。
  7. The result showed that the homology rate of pila gene among the 5 avian pathogenic e. coli strains tested and one human e. coli were from 89. 8 % to 91. 1 %, and the homology rate of amino acid were from 88. 5 % to 91. 8 %. the homology rate of pila gene sequence among 5 avian pathogenic e. coli strains tested and avian pathogenic e. coli reported ( serotype o1, o2, o78 ) were from 87. 8 % to 90. 2 %, and the homology rate of amino acid were from 84. 6 % to 91. 2 %. there had homology in avian pathogenic e. coli. there had some common antigen side in type 1 pili of avian pathogenic e. coli

    結果表明：運用msha法檢測1型菌毛的檢出率為80 （ 36 45 ） ， pcr法的檢出率為95 . 5 （ 43 45 ） ， pcr方法用於1型菌毛的檢測比msha更加敏感、快速、特異性強；選擇5株優勢血清型雞源致病性大腸桿菌代表株（ o _ （ 89 ） ， o _ （ 119 ） ， o _ （ 141 ） ， o _ （ 127 ） ）的1型菌毛pila基因的pcr擴增片段經純化后，分別定向克隆到puc18質粒的多克隆位點，構建了含有目的基因片段的克隆質粒，並轉化到dh5株大腸桿菌載體菌中，篩選獲得陽性克隆菌株。
  8. Clean sand traps and header box to the reserve pit

    把錐型罐和振動篩入口罐的廢鉆井液清到排污池子去。
  9. Technique specification for fine air screen seed cleaner

    風篩式種子清選機.技術條件
  10. On a basis of the developmental inspirations acquired from disputes of “ canon ” for the past half century, this text intends to review the influence of traditional poems collection through procedures of sifting basis and canonization, in hopes of discovering poems collection to be actually the most concrete and effective canon style among traditional poetics ; three types of poetic canons are also concluded within a range of poems collection in ming and ching dynasty

    摘要本文欲藉助近半世紀典律論爭獲得的發展啟示，由篩選基準、正典化等過程上，重新檢視傳統詩選集的影響力，發現詩選集確實是傳統詩文論中最具體而有效力的典律形式；也以明清詩選集為范圍，歸結出三種詩典律的類型。
  11. Improvement of stalk epidermis flap shaker and design of cleaning device for stem sieve

    煙拐剔除篩的改進及煙梗分選篩清理裝置的設計
  12. The consensus statements see appendix recommend the preferred methods of screening for asians, identify the high risk individuals who should be given priorities for screening, and define the role played by family doctors, nurses and healthcare providers

    會議針對適合亞洲人士的篩查方法、高危人士的風險評估、以及家庭醫生、護士和健康工作者所擔當的角色達成了共識，並提供了清晰的指引（詳見附件） 。
  13. Maternal serum human chorionic gonadotropin and alpha - fetoprotein screening for down ' s syndrome

    孕婦血清絨毛膜促性腺激素聯合甲胎蛋白產前篩查唐氏綜合征的研究
  14. The hwtx - i gene was chemically synthesized according to its known cdna sequence, the gene was inserted into vector ppic9k which contained aoxj promotor and the sequence of a secreting signal peptide - a - factor, the cloning ppic9k / hwtx - i was constructed and confirmed by two - step pcr and dna sequence analysis, then it was transformed into host strain gs115, a his + muts cell line was screened and multicopy transformants were screened by various g418 concentrations, the multicopy transformant was named gh1. gh1 was cultivated in flasks. after 6 days of induction by 0. 5 % methanol, the supernatant was checked by 16. 5 % tricine - sds page, which showed there was a band in the position of 3. 5 - 6. 1kd, then it was isolated and desalted by ultrofiltration followed by ion exchange of cm column, after reverse phase hplc of ci8 and vacuum drying, the purified rhwtx - 1 was obtained which was proved to be correct recombinant hwtx - i by tricine sds - page, maldi - tof mass spectrometry, amino acid composition analysis, the n - terminal amino acid sequence and its biological activity, the final field of the purified rhwtx - i was about 80mg / l, accounting for 23. 6 % of it total secretory proteins

    將帶有hwtx -基因的ppic9k經blgii線性化后，轉化酵母宿主菌gs115原生質體后經篩選陽性克隆並經表型鑒定為his ~ + mut ~ s酵母菌，進一步用遺傳毒素g418篩選多拷貝的轉化菌株，命名為gh1 ；將gh1甲醇酵母菌用0 . 5的甲醇誘導表達，發酵上清經90飽和度的（ nh _ 4 ） _ 2so _ 4沉澱， yw - 3 （ mwc03000 ）的超濾膜超濾，再經cm陽離子交換， c _ （ 18 ）反相hplc純化得到分子量為4kd左右的組分，其中4289 . 05的組分經質譜鑒定，氨基酸組成分析和序列測定為正確的表達產物，生物學活性表明其活性為天然毒素活性70 % ，表達量為80mg / l 。
  15. General technical specification for little ballast cleaning machine

    小型道碴清篩機通用技術條件
  16. It is quite evident that the rm - 80 is not suited to working on the harden ling. in order to make rm - 80 be suited to the conditions in china, we conduct an analyse and a calculation theoretically on excavating obstruction, excavating productivity and traction ability sa well. so that we can choose a better matching of produvtivity to solve problem of insufficient ability of excavation

    為使rm80型全斷面道碴清篩機的性能適合我國國情，我們從理論上對該機在板結地段作業時的挖掘阻力、挖掘功率及作業工況下的牽引能力進行計算分析，從而選擇出一種更好的功率匹配關系，解決挖掘能力不足的問題。
  17. On the railway line nuder normal major repair cycle, rm - 80 full section undercutting ballast cleaning machine has enough excavation ability in working condition, productivity can come up with it ' s design standard

    對于正常大修周期的線路上， rm80型全斷面道碴清篩機作業運行工況具有足夠的挖掘能力，作業效率基本上能夠達到其設計標準，這些在國外已經得到了充分的證明。
  18. Those mentioned above has already been proved either in and outside our country. infact, when the machine works on the track which is mudding and hardening, especially on hardening line, rm - 80 can not give full play to it ' s productivity, and sometime the machine can not go forward with excavating chain turnning, which results in a low productivity of not more than 100 meters per hour

    在我們的生產實際中，尤其在板結地段， rm80型全斷面道碴清篩機的作業效率就不能得以充分的發揮，經常出現挖掘鏈轉不動、清篩機不前進，或者是作業效率很低，以致於每小時作業速度不足百米的情況。
  19. Rm - 80 full section undercutting ballast claening machine is made by means of importing the technology from plasser & theuere austria under the way of combining the technology with trade. the machine is of the most advanced level in the world, and played an important role in speeding - up of railway main line in recent years

    Rm80型全斷面道碴清篩機，是鐵道部在1996年採用技貿結合方式，從奧地利plasser & theuere公司引進的全液壓驅動大型養路機械生產製造技術，並由鐵道部昆明機械廠製造生產的。該機械具有當今世界先進水平，並在近幾年鐵路干線提速中發揮了重要的作用。
  20. Testing methods for grain pre - cleaning machine

    糧食初清篩試驗方法
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