細胞毒性試驗 的英文怎麼說

中文拼音 [xìbāodúxìngshìyàn]
細胞毒性試驗 英文
cytotoxic test
  • 細 : 形容詞1 （條狀物橫剖面小） thin; slender 2 （顆粒小） in small particles; fine 3 （音量小） thin ...
  • 胞 : Ⅰ名詞1 （胞衣） afterbirth2 （同一個國家或民族的人） fellow countryman; compatriot Ⅱ形容詞（同胞...
  • 毒 : Ⅰ名詞1 （對生物體有害的性質或物質; 毒物） poison; toxin 2 （毒品） drug; narcotics 3 （姓氏） a s...
  • 性 : Ⅰ名詞1 （性格） nature; character; disposition 2 （性能; 性質） property; quality 3 （性別） sex ...
  • 試 : 名詞（古代占卜用的器具） astrolabe
  • 驗 : 動詞1. （察看; 查考） examine; check; test 2. （產生預期的效果） prove effective; produce the expected result
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  • 毒性 : [藥理學] toxicity; virulence; poisonousness毒性測定 toxicity test
  • 試驗 : trial; experiment; test
  1. In trpsin tolerance assay. this virus could resist to 1 % trpsis at 37 in an hour. in acid tolerance assay, this virus was resistant to ph3. 0 and ph5. 0 at 37 in 2 hours, and the average infection litre of the virus decreased little. in heat assay, at 50, the virus was processed from 5 minutes to 150 minutes and at each condition the viral virulence reduced to some certain degree. among these conditions, when at 50 in 30 minutes. the average infection litre of this virus decreased over 2 tilre. and when al 50 in an hour, cpe of ihis virus disappeared. when time was set for an hour. but with processed in different temperature as 50 60 70, 80, the virus losl the multiplication capacity complelely. in biological assay, we selected different cell lines to cultivate this virus by laking advantage of possesional cells at that time in our laboratory. then we found that fcwf cell line was the most sensitive to dxmv and mdck was the second. with f81 cell line, after passaged for 12 times continuously with low concentration of fcs. the virus could produce cpe. however, with vero cell line. the virus could not procuce any cpe after many passages. the hemagglutination and lumadsorption reaction test proved that this virus had no any reaction to erythrocyte of pig, fowl and cavy. by neutrolizaion assay, dxmv could be identified as a kind of ccv

    理化學研究表明，該病毒為rna病毒，對氯仿、乙醚敏感；胰酶試驗中，經37 、 1小時處理的病毒，仍然能夠在貓源細胞fcwf細胞上生長，並且毒力基本保持不變；耐酸性試驗中，病毒分別在ph5 . 0和ph3 . 0經37作用2小時，毒力僅下降一個滴度；耐熱性試驗中，該病毒在恆定溫度50 ，設定不同時間，從5分鐘到150分鐘，毒力均有不同程度下降，其中， 50作用30分鐘，病毒平均滴度下降2個單位； 50 ， 60分鐘， cpe消失；恆定時間1小時，設定不同溫度（ 50 - 60 - 70 - 80 ） ，病毒在細胞上完全喪失增殖能力， cpe消失。生物學試驗，利用實驗室現有條件，選擇不同的細胞系對該病毒進行培養，發現該病毒對貓源細胞fcwf最敏感； mdck細胞次之； f81細胞經多次傳代，亦可出現cpe ；而vero細胞則不敏感。血凝試驗表明，該病毒對豬、雞、人及豚鼠的紅細胞均無血凝性。
  2. The hemagglutinating characteristic of jl94 was studied tentatively with human and 9 kinds of animal red blood cell ( rbc )

    採集人及9種動物的紅細胞，用病毒的細胞培養物做血凝和血凝抑制試驗，來檢測jl94的血凝特性。
  3. If ip animal health analysis methods - detection of antibodies against mucosal disease by virus neutralisation test and immunochemistry on cell cultures if or ip

    動物健康分析方法.用病毒中性試驗和在細胞上培養
  4. Animal health analysis methods - detection of antibodies against classical swine fever by virus neutralisation test and immunochemistry on cell cultures if or ip

    動物健康分析方法.病毒中性試驗和細胞培養免疫化學檢測典型豬瘟的抗體
  5. The enzyme - linked immunosorbent assay ( elisa ) and high performance liquid chro - matography ( hplc ) analysis for detection of mc were optimized. the removal rates of mc by conventional water treatment processes were investigated through the laboratory study and the detection of mc in every process in meiyuan drinking water treatment plant. results showed that the prechlorination of eutrophic water led to the release of intracellular toxins to water phase

    本文完善了mc的elisa和hplc分析方法，通過模擬試驗及水廠實測調查了富營養化太湖水中mc在常規凈水工藝中的去除特性，結果表明預氯化使藻細胞內的mc釋放出來，混凝沉澱對細胞外mc無去除作用，砂濾可去除17 . 2 40 . 4的細胞外mc和19 . 0 36 . 6的總mc ，加氯消毒對細胞外mc和總mc的去除率分別為30 45 . 3和30 51 . 7 。
  6. This finding may bring a hope to phytoremediate as - contaminated soils. the effects of as and ca on the growth of p. vittata l. and as uptake by p. vittata l. were studied under sand culture condition. the interaction of as and ca on concentration and distribution of metals including k, mg, mn, fe, zn and cu in it were also investigated

    通過砂培盆栽試驗，本論文從砷和鈣的作用對蜈蚣草生長和累積砷的影響及砷、鈣與其他必需金屬元素的關系等方面研究了蜈蚣草的營養特性，從砷、鈣、磷的亞細胞定位探討了蜈蚣草對砷的解毒機理及鈣的作用機制。
  7. Biological evaluation of medical devices - part 5 : tests for in vitro cytotoxicity

    醫療器材的生物評價.第5部分:體外細胞毒性試驗
  8. Mutated plasmid was transformed into e. coli tg1 cells to produce engineered peptide, then the peptide was purified by cm sepharose ion - exchange column. in vitro bactericidal assay and drug withdrawal were used to identify the bioactivity of the engineered peptide. the planar lipid bilayer membrane was used to assay the electrophysiology of the engineered peptide. toxicity studies on mammalian cells were used to assay the toxicity of the engineered peptide

    將重組質粒轉化入大腸桿菌tgi工程菌中，生產構建的工程多膚，離子交換純化后獲得工程多膚初步純化產物，體外抗菌試驗、藥物撤離試驗檢測工程多膚的抗菌活性，在人工脂質膜上測定其形成離子通道的特性以初步研究抗菌機理， ?並觀察其對真核細胞的毒性作用。
  9. The security of cp i according to the experiments of mice accute toxicity was evaluated, guinea pig sensitization and cytotoxicity experiment in integer level and cell level. it showed that : the mice had no toxic reaction ; the guinea pig ' s points of injection had no erythema and dropsy ; the cytotoxicity was lower than i class. the results proved that cp i had no poison side effects

    通過小鼠急性毒性試驗、豚鼠致敏試驗、細胞毒性試驗對自製cp進行整體水平和細胞水平的生物安全性評價，觀察期內，小鼠未見異常毒性反應；豚鼠注射點無紅斑及水腫情況；細胞毒性小於級，結果證明本方法制備的cp無毒副作用。
  10. Biological evaluation of medical devices - tests for in vitro cytotoxicity

    醫療器械的生物評定.在試管內的細胞毒性試驗
  11. Biological evaluation of medical devices - part 5 : tests for cytotoxicity : in vitro - methods iso 10993 - 5 : 1999 ; german version en iso 10993 - 5 : 1999

    醫療器械的生物學評價.第5部分:細胞毒性試驗:試管內
  12. Al toxicity - induced ultraweak luminescence ( ul ), sister - chromatid exchanges ( sces ), programmed cell death ( pcd ) in root tips of barley, al - resistant genetic engineering and the role of root border cells in al toxicity were studied respectively, in order to explore some new pathways for al toxicity, al - resistant mechanism and genetic improvement

    大麥是鋁毒極為敏感的作物，本實驗以大麥為材料，開展了鋁毒誘導的根尖細胞超微弱發光、姐妹染色單體交換（ sce ） 、細胞程序性死亡、耐鋁基因工程及邊緣細胞在鋁毒中的功能研究。試圖為植物鋁毒及耐鋁機制和遺傳改良研究探索新途徑。
  13. Biological evaluation of dental materials. part 2 : biological evaluation test method of dental materials. cytotoxicity tests : agar diffusion test and filter dissusion test

    口腔材料生物學評價.第2單元：口腔材料生物試驗方法.細胞毒性試驗：瓊脂覆蓋法及分子濾過法
  14. Biological evaluation of medical devices - part 5 : test for in vitro cytotoxicity

    醫療器械生物學評價第5部分:體外細胞毒性試驗
  15. The mechanisms of fumonisin - induced toxicity have not been clarified, human and animal cell lines can been used extensively to study its toxicity

    摘要伏馬菌素毒性作用機制尚未研究清楚，目前採用了廣泛的細胞試驗進行研究。
  16. The results revealed that antigenic drift had occurred in virus strains of the same h9n2 subtype in the north of henan province during 1998 - 2002. h9n2 subtype aivs were stable from 1998 to 1999, since the mutual protection between 98a5 and 99s approached to 100 %, which was consistent with results in hi and vn tests

    1998年和1999年h _ 9n _ 2亞型禽流感病毒較穩定， 98a5和99s毒株間的保護力接近100 ，在hi 、雞胚中和、細胞中和試驗結果的相關性均在0 . 74以上，表明兩毒株間的抗原性相近。
  17. Biological evaluation of medical devices - part 5 : test for cytotoxicity : in vitro methods included in ansi aami iso 10993 - 1993 : a collection

    醫療器械的生物學評價.第5部分:體外細胞毒性試驗法
  18. Bypassing the use of mouse cells is not only easier, but it also eliminates the risk that therapeutic stem cells might carry rodent iruses, thereby potentially speeding their approal for testing in humans

    避免鼠細胞的使用不僅使技術更加簡單，而且降低了治療性幹細胞可能會攜帶嚙齒動物病毒的危險，也因此可能加快得到將它們應用到人體試驗的許可。
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