病毒培養 的英文怎麼說

中文拼音 [bìngdúpéiyǎng]
病毒培養 英文
viral cultivation
  • 病 : Ⅰ名詞1 （疾病; 失去健康的狀態） illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • 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...
  • 培 : 動詞1. （在根基部分堆上土） bank up with earth; earth up 2. （有目的地使成長、壯大） cultivate; foster; train
  • 養 : Ⅰ動詞1 （供養） support; provide for 2 （飼養; 培植） raise; keep; grow 3 （生育） give birth to ...
  • 病毒 : [醫學] virus; inframicrobe （濾過性）
  1. The a / pr / 8 / 34 ( hln1 ) adapted to mouse lung was propagated in allantoic cavity of 9 - day - old embryonated chicken eggs and titered by hemagglutinin test, and the tilers was 1 : 320

    用9日齡雞胚培養人流感病毒的鼠肺適應株戶jp側8 / 34 （ hini ） ，通過血凝實驗測得病毒滴度為1 : 320 。
  2. Tissue culture is the most important tool used in virus assay.

    組織培養是用於病毒試驗的最重要的手段。
  3. It is an important that bacteria contaminated vaccine in the biologicals production. we collected 703 samples of cell culture, virus cultivation and harvest which were contaminated by bacteria during poliovaccine production within two years. we checked these samples by bacteriological method and antibiotics sensitivity tests were done. it shows that 1 ) the main contaminated bacteria come from staphylococci, bacilli and streptococci of environment in the poliovaccine production. 2 ） it is effect that antibiotics to contaminated bacteria are doxycycline, albiotic, prescription 2, cefotaxime na salt, gentamycin, neomycin, aureomycin and erythromycin

    在疫苗生產實踐中，細菌污染是影響疫苗質量和產量的關鍵性因素，筆者通過了兩年左右的時間，選取正常生產中零星細菌污染的細胞培養瓶、病毒培養瓶及收毒污染樣品等共703份，進行細菌學檢查，並對造成污染的主要細菌種類進行了各種抗菌藥物的耐藥性實驗，結果表明：我所脊灰疫苗生產中主要的污染威脅來自環境中的葡萄球菌，潛在威脅是桿菌和鏈球菌；強力黴素、林可黴素、配方2 、噻孢黴素鈉鹽、慶大黴素、新黴素、金黴素和紅黴素等抗生素對目前引起污染優勢細菌-葡萄球菌有明顯的抑菌效果，可作為疫苗生產后備抗菌手段參考
  4. Animal health analysis methods - detection of antibodies against caprine arthritis encephalitis virus by the agar gel immunodiffusion test

    動物健康分析方法.用細菌培養基凍膠免疫擴散試驗檢測抗山羊關節炎腦炎病毒抗體
  5. 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。
  6. Based on the survey of viruses infecting araceae plants from in zhejiang province, hunan province, hainan province and other regions in china, pathogenic viruses of this family were detected and identified. sequence similarity was compared between dasheen mosaic virus ( dsmv ) isolates of different origin. virus - free seedlings were obtained for two important taros cultivar, colocasia esculenta cv

    本研究論文對我國浙江省、湖南省和海南省等地的天南星科植物上的主要病毒進行了檢測和分子鑒定，比較了該科主要病原病毒芋花葉病毒（ dsmv ）不同分離物的序列同源性並分析其種內分化關系；同時，我們對2種重要的芋屬栽培作物? ?奉化芋艿頭、烏梗芋（ colocasiaesculenta ）和我國特有的天南星科藥用植物? ?掌葉半夏（ pinelliacordata ）進行了脫毒培養和快速繁殖研究。
  7. Cultivation of avian encephalomyelitis virus in cef

    利用雞胚成纖維細胞培養禽腦脊髓炎病毒的研究
  8. 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。
  9. 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
  10. 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
  11. The induction of a tumor by a virus in vivo can be reproduced in tissue cultures.

    病毒在體內誘發腫瘤可以在組織培養中再現。
  12. Gpv ( goose parvovrius ) has been classified by its morphological, biochemical, and clut - ure characteristics as a member of the parvovirus genus of the parvoviridae. lt is a highly fatal disease of gos1ings and muscovy ducklings, the typical pathological lesions was found in digest tract, specially in small intestine

    Gpv （ gooseparvovirus ）依據其形態、生化及培養特性被劃歸為細小病毒科細小病毒屬成員，引起雛鵝和雛番鴨高度致死性疾病，主要以消化道，尤其是小腸部位的典型病變為特徵。
  13. The supernate of virus culture was used as templet in overlapping pcr, then the interesting gene was obtained

    利用重組pcr的方法，以病毒培養液上清為模板，把二個目的基因串聯在一起。
  14. Propagation of virus in embryonating eggs was first used by goodpasture and woodruff in 1931.

    1931年Goodpasture和Woodruff首次應用雞胚培養病毒。
  15. Cucumber mosaic virus resistant mutant from tobacco ' s anthers treated with ray through anther culture

    輻射與花藥培養相結合篩選煙草抗黃瓜花葉病毒病突變體
  16. The transgenic plants have been studying for more than ten years, which have some advantages including that the plants are autotrophy not requiring expensive media or strict culture conditions, and the plant viruses cannot infect human, compared with other systems such as microbe fermentation and transgenic animals

    與微生物發酵、動物細胞和轉基因動物等生產系統相比，轉基因植物不需要昂貴的設備和嚴格的培養條件，具有光合自養、成本較低，植物病毒不感染人類等優點，已成為一類比較廉價和安全的生物反應器。
  17. Yu - chan chao at the institute of molecular biology, academia sinica, constructed a recombinant baculovirus

    在貼附培養的情況下，此病毒感染宿主昆蟲細胞不會造成昆蟲細胞溶裂。
  18. Second, some reports utilized the baculovirus as a gene delivery vehicle into mammalian cells and did not have any bad effect on the growth of mammalian cell

    因此，本論文中討論一些影響蛋白質表現量與延長表現的參數如:培養基的更換、重復感染、病毒感染方式。
  19. Study of hc replication within lier cells, or hepatocytes, has been hampered by a lack of adequate irus culture systems

    有關hc在肝臟細胞復制繁殖的很多研究，因為缺乏足夠的病毒培養體系而被迫停止不能進行下去。
  20. This culture system proides a breakthrough in studying hc replication in nontransformed hepatocytes, the natural target of the irus

    該病毒培養系統是非突變肝細胞內hc復制擴增技術的突破。
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