集體檢疫 的英文怎麼說
中文拼音 [jítǐjiǎnyì]
集體檢疫
英文
group quarantine-
One group was immunized with cdv vaccine, and the other group was cav. serum samples and eggs were collected weekly for detected antibody titers. high titer egg yolk was collected for following igy extraction
分別用cdv 、 cav的疫苗免疫產蛋雞，每周檢測雞血清和卵黃中的抗體水平，收集抗體水平高的雞蛋用於提取純化卵黃抗體igy 。The main products became a shortlist of national pipeline bureau in 2000 ; passed through iso9001 - 2000 international standard quality system certification in 2001 ; ranked as recommended products by china petrol - chemical group and successively obtained physical market entrance permissions awarded by major oil fields within nationwide in 2002 ; audited to be a membership of china petroleum distribution corp. ( energy ahead ) in 2003 ; gained pressure conduit component manufacture license ( for products such as insulation joint, fast - opening blind, receiver & launcher, etc. ) awarded by the general administration of quality supervision, inspection and quarantine of the prc in 2004 ; and obtained pressure vessel manufacture license in 2005
公司主要產品於2000年成為國家管道局入圍產品； 2001年通過了iso9001 - 2000國際標準質量體系認證； 2002年被中國石油化工集團列為推薦產品，並先後獲得國內各大油田的物質市場準入證； 2003年經審核成為中國石油銷售總公司（能源一號網）會員單位； 2004年遼寧省首家獲得（絕緣接頭、快開盲板、收發球筒有關產品）中華人民共和國質量監督檢驗檢疫總局頒發的壓力管道元件生產製造許可證； 2005年取得了壓力容器生產製造許可證。Methods : 1 ) 12h after irradiation, the cell cycle of nih3t3 cells was determined by flow of cytometry and the ratio of alternations in p16 gene exon - 2 was evaluated through pcr - sscp. 2 ) the content of mda, the activities of the sod and gsh - px in the supernatant of nih3t3 cells and the cells were measured by detecting kits immediately after irradiation. 3 ) the level of matrix metalloproteinase - 2 ( mmp - 2 ) in hela cells was detected by western - blotting and dot - blotting 2h after irradiation
具體方法為： （ 1 ）照射后12h ，收集nih3t3細胞，用流式細胞儀檢測各組細胞的細胞周期， pcr - sscp檢測抑癌基因p16的變化； （ 2 ） nih3t3細胞照射后立即收集細胞和細胞上清，用試劑盒測量mda含量和sod 、 gsh - px的活性並觀察其變化； （ 3 ） western免疫印跡和點雜交法檢測照射2h后的各組hela細胞中基質金屬蛋白酶- 2 （ mmp - 2 ）的表達變化。No trace of any newly expressed protein band was noticed in supernant as well as in the cells by sds - page, except the verification of the substitution of beta - galactosidase gene ( the lose of galactosidase protein band ), which is a selective marker of the wild - type virus. elisa test results suggested the expression of egf in cells, but not in culture supernant. the quantitative calculation suggested the expressed egf was about 6 - 7 u g ( as egf standard ) per flask ( 2 > < 106 cells ) in the cellular extract
將重組病毒rbmbacph - egf以10moi感染bmn細胞， 72小時后收集培養細胞和上清；培養上清和經超聲波處理的細胞樣品elisa檢測發現胞內樣品中存在能與egf抗體免疫反應的產物，粗略估計表達量約6 7 g 2 10 ~ 6個細胞（相當于egf標準品） ；重組病毒rbmbacph - egf穿刺接種5齡家蠶幼蟲，每隔24h收集蠶血淋巴，經elisa檢測發現第4天表達量最高，根據egf標準曲線計算蠶血淋巴的表達量約32 g ml ； elisa定性實驗還發現正常蠶血也存在與egf抗體間交叉反應的物質。The results showed that the total coincidence rate between digfa and sat and the coincidence on positive rate of detection were 99. 88 % ( 4003 / 4008 ) and 94. 25 % ( 82 / 87 ), respectively, and the sensitivity of digfa appeared to be higher in population with brucellosis and in high - titered serum samples
方法用已建立的布病滴金免疫測定技術檢測不同職業和不同感染類型人員的布病抗體，並與布病試管凝集試驗作平行檢測。In particular, travel advisories and precautions, screening of persons arriving from affected areas, closing schools, restricting public gatherings, quarantine of exposed persons and isolation of infected persons may be implemented with the intent of slowing introduction and transmission of the virus
規劃還指出，如果證實禽流感病毒可通過咳嗽或噴嚏在人體間蔓延，則可能發布旅行建議和旅行警告，關閉學校，限制集會和採取檢疫措施。Now we are building the transmission center which includes : ca cold - storage warehouses, information management system, detection system of agriculture chemicals residue, inspection system of plant diseases and insect pests, fruit processing system, packing factory, transportation system
目前，我公司正在進行庫爾勒香梨物流配送中心項目的建設，該物流配送中心是集保鮮儲藏、信息管理系統、農藥殘留檢測，病蟲害檢疫、冷藏運輸、自動加工分檢、物流包裝為一體的現代化物流配送中心。Now the biological and molecular assays are the major methods to assay cpti transgenic plant. there is no better method on assaying the expression of the transgene. the reason would be that the outcome of expression by cpti is a little peptide and its molecular weight is very small. its immu - nogenicity would be insufficiency so that it can not induce strong immu - nological reaction and can not produce special antibody of high potency
目前對轉cpti基因植物的檢測主要集中在生物測定和分子檢測，尚無較好的基因表達產物的檢測方法，其主要原因在於cpti基因的表達產物是小分子多肽，分子量小，免疫原性不夠，直接免疫不足以產生較強的免疫反應，不能產生效價高的特異性抗體。分享友人