血清病毒法 的英文怎麼說

中文拼音 [xiěqīngbìngdúfǎ]
血清病毒法 英文
serum virus method
  • 血 : 血名詞（血液 多用於口語） blood:吐血 spit （up） blood; 血的教訓 a lesson paid for [written] in b...
  • 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...
  • 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...
  • 法 : Ⅰ名詞1 （由國家制定或認可的行為規則的總稱） law 2 （方法; 方式） way; method; mode; means 3 （標...
  • 血清 : [免疫學] serum; blood serum血清病 serum sickness
  • 病毒 : [醫學] virus; inframicrobe （濾過性）
  1. Capsid proteins are involved in recognition and infection of the host and can be used to identify the virus by serological means or amino acid sequencing

    衣殼蛋白與寄主的識別和感染有關，還可以通過血清學的方法或氨基酸序列來識別病毒。
  2. Administration of veterinary biologic and animal drug in the united states of america is belongs to two agency : aphis - cvb and fda - cvm. mostly the legal basis for product licensure include : vst acts, 9cfr, vsm, federal food, drug, and cosmetic act, 21cfr etc. the european medicines evaluation agency for product used in animal is emea - cvmp. the legal basis on three director ( 81 / 851 / eec, 81 / 852 / eec, 2001 / 82 / eec ) and one regulation ( 2309 / 93 / eec )

    美國獸用生物製品和獸用藥品歸兩個部門管理，獸用生物製品由美國農業部動植物檢疫局（ aphis ）下屬的獸醫生物製品中心（ cvb ）負責，獸用藥品由美國健康和人類服務部食品與藥物管理局（ fda ）下屬的獸醫藥品中心（ cvm ）負責；產品注冊的有關法律法規主要包括生物製品的《病毒-血清-毒素法》 （ vstacts ） 、 《聯邦法規9 》 （ 9cfr ）及一些規章如美國獸醫局發布的《美國農業部獸醫服務局規章》 （ vsm ）等，獸用藥品的《聯邦食品、藥品與化妝品法》和《聯邦法規21 》等。
  3. 10. 14. 25 and 30 days post injection and separated the serum. meanwhile, pathological changes of lymphocytes and changing role of igm, igg from different days old chickens infected with aev - nh937 were systematically studied by viral inoculation of animal, pathological test and elisa

    採用了病毒接種技術、普通病理學方法、酶聯免疫吸附實驗等方法，研究了不同日齡spf雛雞人工感染aev - nh937株后的血清igm 、 igg的動態變化規律。
  4. Micro - serum neutralization test, virus isolation and identification for bluetongue

    藍舌病微量血清中和試驗及病毒分離和鑒定方法
  5. The diaphragm had the ability to detect the positive serum when it was diluted to 2 ' 11 and so it has good sensitivity ; stored at 4 for at least 7 months, the sensitivity and specificity of the diaphragm did not change, so it has good stability ; when 10 positive serum was detected 3 times, the result is reproducible, so the diaphragm has good reproducible. serums from experimental inoculated piglets was detected. the results showed that when the titer is l : 16, the pigs were infected with streptococcus suis ; and when 1 : 64, the pigs could survive after challege with streptococcus suis. all the results have shown that dot - ppa - elisa was a convenient, rapid, sensitive specific useful method for the detection of antibody

    該法以硝酸纖維素膜為固相載體，包被膜載抗原製成的診斷膜片具有良好的特異性：不與仔豬副傷寒、豬巴氏桿菌病、豬大腸桿菌病、豬衣原體病、豬瘟、豬細小病毒病、豬偽狂犬病、豬布氏桿菌、豬丹毒陽性血清反應；膜片具有良好的靈敏性，陽性血清作2 ~ （ - 11 ）稀釋亦能檢出；膜片具有良好的穩定性，在4至少能保存7個月，其靈敏性不變。
  6. Hbv genotype was determined by the restriction fragment length polymorphism analysis in patients with chronic hbv infection in 5 cities of fujian province. 2. the sensitivities and specialties of melting curve assay and pcr microplate hybridization - elisa assay were compared with mpcr - rflp and sequence analysis for the detection of hbv ymdd mutants in 44 serums from patients receiving lamivudine monitherapy with viral breakthrough

    應用熔解曲線法和pcr微板核酸雜交- elisa法對44例接受拉米夫定治療過程中出現病毒學反跳時的血清進行ymdd突變株的檢測，並與測序法和mpcr - rflp法比較它們的敏感性、一致性。
  7. Conclusion this is a serum - free culture system for developing a conjunctival epithelial explants with improved purify and proliferative, which are important for the basic research and tissue engineer of conjunctival epithelial cells

    結論無血清培養系統的組織塊培養法可為結膜上皮細胞的疾病、藥理毒理研究及培養移植的結膜上皮細胞提供更為安全有效的細胞模型。
  8. Out of the 26 mutants detected by mpcr - rflp, only 16 and 18 mutants were found by melting curve assay and pcr microplate hybridization - elisa, respectively

    5 . 44份出現病毒學反跳的血清，用mpcr一盯lp法檢測26例為ymdd突變株， 18例為野生株。
  9. Laboratory tests at cdc ? including several pcr - based assays, serologic tests, electron microscopy, immunohistochemistry, and gene sequencing ? confirmed these results and showed that the virus is m # 111nkeypox virus

    Cdc的實驗室測試包括幾個以pcr為基礎的化驗、血清學測試、電子顯微鏡方法、免疫歷史化學和基因序列確認了這些結果並表明這種病毒是猴痘病毒。
  10. The detection for clinical blood serum shows that dna electrochemical sensor can find out the hepatitis b virus dna in blood serum, and the relative concentration of dna was consistent with that abtained by fluorescence polymerase chain reaction

    對臨床血清的檢測表明， dna電化學傳感器能夠檢測出血清中存在的乙肝病毒dna ，並且其相對濃度大小與通過熒光聚合酶鏈反應法得到的結果具有一致性。
  11. Detection antibodies against foot and mouth disease virus - protocol of micro - serum neutralization test

    口蹄疫病毒抗體檢測方法.微量血清中和試驗
  12. The expression of recombinant infectious bursal disease ( ibdv ) vp2 gene in transgenic tobacco was studied. it revealed that the vp2 produced in transgenic tobacco could react with serum specific for ibdv. these results were the basic of investigating the immunological function of foreign protein vp2 produced in transgenic plants and bolstered the concept of using transgenic plants for a novel, edible, safe vaccine production

    研究了傳染性法氏囊病病毒抗原蛋白基因ibdvvp2在煙草中的表達情況，證明轉基因煙草中產生了能與ibdv特異抗血清反應的ibdv抗原蛋白，為研究轉基因植物中生產的外源蛋白vp2的免疫學功能奠定了基礎，並為利用轉基因植物生產可食疫苗提供了實驗依據。
  13. The disease was diagnosed mainly ac : cording to lts clinico - pathology and combining the serologica1 and virological methods, but most of those methods were time - consuming and laborious, which delay the cure, so it is necessary to develop a rapid, simple and special diagnostic method

    目前主要依據臨床癥狀結合血清學、病毒學方法診斷該病，這些方法大多費時、費力，容易延誤該病的治療，需建立一種快速、簡便、特異的診斷方法。
  14. " cooling of the nose slows down clearance of viruses from the nose and slows down the white cells that fight infection.

    鼻子著涼使得白血球無法及時投入與感冒病毒作戰的主戰場，從而延緩了對那些病毒的清除。 」
  15. In conclusion, the diagnostic methods we developed for immunological markers of hepatitis b virus by using time - resolved fluoroimmunoassay, eu - dtta as label, have wide assay ranges, high sensitivity and specificity. they would have widely application in the further research work and clinical diagnosis

    總之，我們利用eu - dtta為標記物建立的乙型肝炎病毒五項血清學標志物時間分辨熒光免疫分析法分析范圍寬，靈敏度高，操作簡便，具有優越的定量檢測能力，十分適合臨床推廣應用。
  16. In this study, pichia pastoris system had been utilized for expression of fmdv 2c3abc gene which aimed for establishing a sensitive and specific molecular dignosis method. first, 2c and 3abc genes were amplified individually from p2 and 3abc postive clones and ligated together using pcr method, then this 2c3abc product was cloned into pgem - t easy vector and transformed e. coli dh5a competent cell. a postive recombinant plasmid which contained whole 2c3abc gene had been confirmed by pcr, enzyme digestion and sequencing. after that, the 2c3abc gene was sub - cloned into ppiczaa expression vector and transformed e. coli dh5 a competent cell and selected by zeocin ? antibiotic. the postive recombinant expression vector was linerized and electro - transformed pichia pastoris smd1168 competent cell. a recombinant pichia pastoris had been obtained by zeocin ? antibiotics selection and induced with 0. 5 % methanol for target protein expression. the expression product was analysised by sds - page and western blotting assay. the result sh owed that 2c3abc gene was expressed successfully in pichia pastoris and the product was a 95ku fusion protein which could be recognized by anti - fmdv serum. the amount of target protein was over 15 % of the total bacteria protein by gel thin layer scanning analysis. this research had supplied materials for establishing a fmd diagnosis method to differentiate infected animals from vaccinated animals

    首先，用p2和3abc陽性克隆通過連接pcr方法獲得目的基因並將其克隆到pgem - teasy載體上，並轉化e colidh5a感受態細胞中，經pcr 、酶切以及測序證明得到了完整的2c3abc基因，並與國內外參考序列進行比較分析。然後，將目的基因亞克隆于ppiczaa表達載體並轉化大腸桿菌dh5a ，以zeocin ~ （ tm ）抗性篩選陽性克隆，大量提取重組表達質粒並用pme酶線性化后電轉化入畢赤酵母smd1168感受態細胞，通過zeocin ~ （ tm ）抗生素梯度濃度篩選，獲得重組酵母用0 . 5甲醇誘導表達，通過sds - page電泳、 westernblotting分析，結果表明， 2c3abc基因在畢赤酵母中成功表達，其表達產物為一95ku的融合蛋白，並能被口蹄疫病毒陽性血清識別。
  17. This has helped them to find two quick ways of diagnosing the disease in the laboratory, which involve examining the serum of sars patients. this is because a person will develop anti bodies once being attacked by certain viruses and the anti

    非典的兩種確診方法都涉及到檢查患者血清，患者一旦被病毒攻擊，將會產生抗體，而且抗體留在血清里。
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