昆蟲病毒 的英文怎麼說

中文拼音 [kūnchóngbìng]
昆蟲病毒 英文
insect viruses
  • : 名詞1. (哥哥) elder brother2. [書面語] (子孫; 後嗣) offspring 3. (姓氏) a surname
  • : 名詞1. (蟲子) insect; worm 2. (姓氏) a surname
  • : Ⅰ名詞1 (疾病; 失去健康的狀態) illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • : 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...
  • 昆蟲 : insect
  • 病毒 : [醫學] virus; inframicrobe (濾過性)
  1. Entomologist stephen doggett, who runs the nsw health arbovirus program which monitors mosquitoes and the diseases they carry is firmly in the deet ( diethyl toluamide ) camp

    負責新南威爾士衛生局項目的學家斯蒂芬?多格特贊成使用避蚊胺。該項目監控蚊子和它們自身攜帶的多種疾
  2. The inspection items include harmful existences ( pathogenic microbes, celozoic and ectozoic parasites, insects, weeds and other harmful substance ) ; residues ( pesticides and veterinary drug residues, heavy metal, chemical toxins, toxic substances, trace elements ) etc

    檢驗項目包括有害生物(原微生物,體內、外寄生、有害物質、雜草等) 、殘留(農藥與獸藥殘留,重金屬,生物與化學素,有物質,超標的微量元素)等。
  3. The bluetongue virus replicates in the insect.

    藍舌在這種體內繁殖。
  4. Production of insulin - expressing adeno - associated virus using baculovirus system

    利用昆蟲病毒系統生產表達胰島素的腺相關
  5. Yu - chan chao at the institute of molecular biology, academia sinica, constructed a recombinant baculovirus

    在貼附培養的情況下,此感染宿主細胞不會造成細胞溶裂。
  6. They are also the key components of insect - baculovirus expression system ( bevs ), which has been one of the four main expression systems in gene engineering

    同時,桿狀細胞表達系統是一類重要的真核表達系統,現已成為目前基因工程四大表達系統之一。
  7. In the adherent culture, the virus did not result in cell lysis after the insect cells were infected

    而在本論文中,我們嘗試將此一非溶裂細胞/桿狀表現系統轉移到旋轉瓶的懸浮培養。
  8. Baculovirus / insect cell system has been widely used for recombinant protein production, but traditional system eventually resulted in cell lysis, so that the expressed recombinant protein was lost into medium

    摘要:桿狀/細胞系統已經被廣泛的應用在重組蛋白質的生產上,但傳統的桿狀感染后會造成細胞溶裂,而使得表現出的重組蛋白質流失到培養基中。
  9. Meq protein, highly expressed in the insect cell line sf9 by the baculovirus vector was immunized into balb / c mice and the immunized spleen cells were collected and fused with the tumor cell line sp2 / 0 via peg - 1000 in vitro. the hybridoma cells were cloned and screened for the ability of anti - meq mcab secretion by fa with the mdv ga infected chicken embryo fibroblast ( cef )

    利用通過桿狀載體在細胞系sfg上高度表達的meq蛋白產物免疫balb / c小鼠,然後收獲其免疫脾細胞並與腫瘤細胞系spz / 0通過peg于體外融合;獲得的雜交瘤細胞被克隆並通過與mdv感染的雞胚成纖維細胞( cef )做免疫熒光試驗( fa ) ,進行其分泌抗meq單克隆抗體( mcab )能力的篩選。
  10. Results we construct recombinant angiostatin baculovirus with a high virus titer ( 2 + 108 pfu / ml ) successfully. recombinant angiostatin was effectively expressed in insect cells ( sf9 ) as 53 kd fusing protein and its expression level was about 90 % of insect cellular total soluble proteins. the recombinant angiostatin protein could inhibit endothelial cell proliferation in vitro with ic50 value of 2

    實驗結果我們成功地構建了滴度高達2x10 『 pm llil的angiostatin重組? 2 ?桿狀,並在細胞sffi中高效表達了分子量為53kd的an giostatin重組蛋白,重組angiostatin蛋白不僅在體外顯著抑制內皮細胞的生長, k 。
  11. Polydnavirus gene products and their physiological effects on host insects

    的基因表達產物及對寄主的生理作用
  12. Baculoviruses are arthropod specific viruses that have long been used as biological agents to control the insects attacking crop plants

    摘要桿狀是鱗翅目的重要原微生物,在重要農業害的生物防治中具有很大的應用前景。
  13. Advance of researches on insecticidal toxins from symbiotic bacteria of entomopathogenic nematodes

    原線共生菌殺素研究進展
  14. Identification and activity of antibacterial substance from xenorhabdus nematophila var. pekingense

    原線共生細菌發酵液對棉鈴和菜青的口服
  15. Article 10 upon the arrival of containers, goods, or discarded used materials at the port ready for shipping in or out, the shipper, the carrier ' s agent or the consignor is required to report to the health and quarantine organ for inspection

    對來自疫區的、被傳染污染的以及可能傳播檢疫傳染或者發現與人類健康有關的嚙齒動物和的集裝箱、貨物、廢舊物等物品,應當實施消,除鼠、除或者其他必要的衛生處理。
  16. Insects such as aphids carry viruses from plants to plants as they feed, and mites and nematodes can also carry disease

    中的蚜在攝食時可以將所攜帶的從一個植物體傳播到另一個植物體,類似的還有老鼠和線等也可以攜帶
  17. Herpesiruses descended from a strain that once infected a common ancestor of mammals, birds and reptiles

    皰疹源於一度感染哺乳動物、鳥類和的始祖的株。
  18. In this experiment hcv structural gene was amplified by polymerase chain reaction ( pcr ), and was inserted into baculovirus expression vector pfastbacl to construct a recombinant transposing vector pfbl - cee. the plasmid pfb 1 - cee was transformed into dh1 obac competent e. coli cells. high molecular weight dna was prepared from the overnight cultures from the selected e. coli colonies, which was recombinant baculovirus shuttle vector containing hcv structural gene, named bac - cee

    本實驗用pcr擴增hcv結構區基因,克隆到桿狀表達載體pfastbacl中,構建成重組轉座載體pfb1 - cee ,轉化dh10bac大腸桿菌感受態細胞,篩選陽性菌落,抽提大分子質粒dna ,獲得含hcv結構區基因的重組桿狀穿梭載體bac - cee ,脂質體介導轉染sf9細胞,出現細胞變后,收集含有重組桿狀顆粒的培養上消,重新感染sf9細胞,收集sf9細胞,進行12 . 5 sds -聚丙烯酰胺凝膠電泳,可見表達的蛋白條帶。
  19. The ha 122 protein, when fused to gfp was observed in the nuclei of h. armigera cells, but only in conjunction with wild type hasnpv infection

    將ha122與綠色熒光蛋白( gfp )基因融合,在細胞中瞬時表達。當有感染同時發生時, gfp信號定位在核內。
  20. In order to get the soluble recombinant eo protein and inspect the protein expression status convinently, the egfp and eo gene were ligated into baculovirus transfer vector. with the co - transfecting sf9 cells of baculovirus recombinant transfer vector and linearized viral dna, and plaque purification in the posttransfection procedure, the pure recombinant baculovirus were harvested, which infected the sf9 cells for amplifying to generate a p - l stock. in the meantime, the fluorescence microscopy detection indicated expressed egfp protein to confirm the heterogenous protein expression of recombinant baculovirus. the pi - stock from a pure plaque was used to generate a high liter p - 2 stock, which was determined in liter as 1. 14 107pfu / ml by performing a plaque assay. when a volume of p - 2 stock infected the sf9 cells with moi 5 - 10 for expression, the strong fluorescence was obeserved on the day 3 of postinfection

    此外,為了得到可溶性重組eo蛋白並便於觀察重組蛋白的表達情況,我們將egfp基因與eo基因相連插入桿狀轉移載體中,與線性桿狀dna共轉染sf9細胞后通過噬斑純化得到純的重組桿狀,將其感染sf9細胞制備p1種子液,同時用熒光顯微鏡觀察綠色熒光蛋白的表達情況剔除表達效果差的重組桿狀。再用p1種子液感染sf9細胞制備高效價的p2種子液。通過液的梯度稀釋和噬斑測定,確定p2種子液的滴度達1 . 14 10 ~ 7pfu ml 。
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