篩組 的英文怎麼說

中文拼音 [shāizǔ]
篩組 英文
nest of screens
  • 篩 : 名詞[書面語] （植物名） sedge
  • 組 : Ⅰ名詞1 （由不多的人員組成的單位） group 2 （姓氏） a surname Ⅱ動詞（組織） organize; form Ⅲ量詞（...
  1. Newcastle disease virus ( ndv ) strain 695, a thermostable nature avirulent strain, were replicated in embryonated chicken eggsand its rna was extracted from allantoic fluid. referred to the reported sequence of f gene, a pair of primers were designed and synthesized. f gene of ndv b95 strain was amplified by rt - pcr, the pcr products were checked by agrose gel electrophoresis and purified by agrose gel fracion method

    利用從國外引進的新城疫熱穩定性天然弱毒b _ （ 95 ）株接種spf雞胚繁殖病毒，經處理后提取病毒的基因組rna ，參考國內外發表的ndv融合蛋白基因序列，設計一對特異性引物，經反轉錄聚合酶鏈式反應（ rt - pcr ）擴增出約1700bp大小的特異性片段，將此片段回收純化后，利用t - a克隆技術將其克隆到pgem - t - easy克隆載體中，再轉化大腸桿菌jm109感受態細胞，轉化后經分子量比較、 pcr鑒定和酶切分析篩選陽性克隆。
  2. The total rna was isolated from pokeweed ( phytolacca americana ) leaves using the method of guanidine isothiocyante and used as template to amplify the total length and deleted mutant pokeweed antiviral protein ( pap ) gene by rt - pcr and then the pap gene was cloned into pgem - t vector. the sequencing results showed that pap gene had 99. 9 % identity comparing with the pap gene nucleotide sequence reported by lin et al ( 1991 ). the iptg - inducible expression vector containing the pap gene was constructed and transferred into e. coli bl21 ( de3 ) - plyss

    將缺失型pap基因克隆到植物表達載體pbi121中，通過液氮冷凍法將重組質粒轉入農桿菌lba4404細胞中，然後採用葉盤法，在該農桿菌的介導下將pap基因導入普通煙草中，經過卡那黴素抗性篩選，最後獲得了轉pap基因的工程煙草植株，摩擦接種煙草花葉病毒（ tmv ） ，與非轉基因煙草相比，能夠推遲癥狀表現達2月之久，說明pap基因能夠在其它植物體內產生有活性的高抗病毒的蛋白質。
  3. This paper introduced the application of biotechnology in rice genetics and breeding, including tissue culture, cell mutants selection, protoplast fusion, apomixis, molecular mark assisted breeding and genic transformation

    簡要綜述了生物技術在水稻遺傳育種中的應用，主要包括組織培養、細胞突變體的篩選、原生質體融合、無融合生殖以及分子標記輔助育種和轉基因技術等方面。
  4. Result : there were statistical differences between the adult group and the pediatric group in ethmoid bulla hypertrophy and middle nasal concha etherealization

    結果：篩泡肥大和中鼻甲氣化的出現率在成年組和未成年組差異有統計學意義。
  5. Methods : we have divided the 636 molars ( without dental caries or pathological changes of root ) collected in school of forensic medicine and stomatological hospital in shanxi medicine university into four groups : maxl, max2, manl, man2, and selected 5 indexes closely related to changes of dental age ( dental attrition, contact area, the index of dentine marrow cavity, the thickness of cementum of root, the diaphaneity of dentine of root ), and proposed the grading standard and scoring standard date processing and statistical analysis after measuring the teeth of the four groups

    方法：從山西醫科大學法醫學院及口腔醫院收集的636磨牙（無齲壞、無根尖病變）分為max1 、 max2 、 man1 、 man2四組，根據牙齒的增齡變化特點，篩選了5個與牙齡變化密切相關的指標（牙齒的磨耗、接觸區面積、牙本質髓室指數、根尖牙骨質的厚度、根尖牙本質透明） ，提出了指標的分級標準和評分標準，對各組的牙齒測量后進行數據處理和統計分析。
  6. Product introduction series of bs undulate screen, which surface are made of more line - up and row peach shape screen pieces, its rotor is circumrotate by same direction and equal speed, the screen surface intervene turning make of levity screen hole, drive materiel above screen go forward with undulate form, thereby reach to separate effectively

    產品介紹bs系列波動篩分機是由轉子上多排多元並列的特製桃形篩片組成篩面，轉子以同向等速做周向旋轉，篩片交錯回轉構成多變的篩孔，使篩上物料以波動形式向前運動，從而達到高效篩分之目的。
  7. 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。
  8. Immunofluorescence - histochemical changes of the astrocytes in cribriform plate due to high intraocular pressure in rats

    大鼠高眼壓后篩板區星形膠質細胞的免疫熒光組織化學變化
  9. Initial penetration of the anterior ethmoid is performed inferomedially using blakesley forceps. this avoids injury to the lamina papyracea laterally, and to the cribriform plate superiorally

    氏鉗向中下開放前組篩竇，以免損傷側面的紙樣板和上方的篩板。
  10. Both intraductal and infiltrating ductal carcinoma are seen here. note the intraductal component in the center with cribriform pattern and prominent microcalcifications. surrounding this are infiltrating carcinoma cells

    同時看到導管內癌與浸潤性導管癌。值得注意的是中心處篩型且有明顯微鈣化的導管內癌組成部分。其周圍是浸潤性癌細胞。
  11. 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。
  12. This sphenoid can also be approached through the ethmoid sinus. approximately 7 cm from the nasal spine,

    也可以通過后組篩竇進入蝶竇，從鼻脊向後約
  13. When disease involves the sphenoid, the sinus can be penetrated either intranasally or through the posterior ethmoid

    當病變累及蝶竇，可以經鼻內和后組篩竇進入蝶竇。
  14. The posterior ethmoid cells are easily identified as they are larger, wider, and fewer in number than anteriorly

    后組篩竇的氣房一般大而寬，在數量上也少於前組篩竇，容易確定。
  15. Objective : to explore anatomical variations of the anterior ethmoid sinus in chinese people and to provide reference for clinical management

    摘要目的：探討國人前組篩竇的相關解剖變異，為臨床手術提供參照數據和資料。
  16. According to these problems, we adopt to the method of mending material, optimize to fermentation media and partly ferment condition. finally, we excogitate a kind of fermentation technology that is suitable for target gene efficiency expressed and is advantageous of product purified. with the plasmid pbv220 - ifnr, pbv220 - hgfa, pbv220 - hgfb, pbv220 - hpk5 that expresses serve as the model, adopting the biostat - c15l of b. braun company, utilize the method of mending material to ferment, through optimization fermentation media and optimization partly ferment condition ( ventilate quantity, stir speed, mend material speed ), eventually establishment a kind of fermentation technology that is suitable for target gene efficiency expressed and is advantageous of product purified

    以我室構建並穩定表達的重組質粒pbv220 - - ifn 、 pbv220 - hgf 、 pbv220 - hgf 、 pbv220 - hpk5為模型，分別從不同的表達宿主菌中篩選出一種適合大規模生產的菌種bl21 （ de3 ） ，該工程菌株連續傳代100代表達質粒不丟失，表達量穩定；採用b . braun公司的biostat - c15l自控發酵罐，運用分批補料技術分別進行四種工程菌的高密度發酵，通過優化工程菌發酵的培養基配方及優化部分發酵條件（通氣量、攪拌速度、補料速度） ，最終建立一種適于目的基因高效表達的高密度發酵工藝模式。
  17. 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。
  18. The newly molted 5th instar larva of silkworm bombyx mori was infected with the recombinant virus

    另外，通過共轉染和篩選純化獲得了攜帶appa基因的重組家蠶桿狀病毒。
  19. Its features are high in rate of making rice, little consume in electricity, small in occupying area, not nessary for special building, convenient in installation and maintenance

    其中12型三聯提升機，二道碾米機有拋光機，三層碎米分級篩組成，成品米為免淘精潔米。
  20. However, as far as the surface of nature sepiolite is concerned, its acidity is weak, and the channel is narrow, and its thermo - stability is poor, which lead to defects such as the destroying effect on the component structure of molecular sieve on the condition of water steam

    但天然海泡石存在表面酸性弱，通道小，熱穩定性差以及在水蒸氣條件下對分子篩組分結構有破壞作用等缺陷，故對天然海泡石進行改性是使其成為催化劑載體所必作的工作。
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