antigen analysis 中文意思是什麼

antigen analysis 解釋
抗原分析
  • antigen : n. 【醫學】抗原。
  • analysis : n. (pl. -ses )1. 分解,分析;【數學】解析。2. 梗概,要略。3. 〈美國〉用精神分析法治療(= psychoanalysis)。
  1. The western blot analysis show that the antiserum induced by the new antigen plus hemocyanin could bind with the 22kd and 55kd proteins, which were existed in the testis tissue protein of mouse, rat and human. 2 ) the purified peptide emulsified in an equal volume of freund ' s adjuvant and immunized the female balb / c mice with 8 - 10 weeks old. the antiserums and the washings of vaginal membrane were detected by elisa, and shown the highest level of the specific antibody igg was 1 : 6000, while the iga was 1 : 300

    二、 p3多肽與弗氏佐劑混懸后免疫近交系balb c小鼠后,在血清和陰道粘膜沖洗液中可檢測出特異性lgg 、 lga ,最高效價分別達到1 : 6000和1 : 300 ;免疫后的小鼠脾臟淋巴細胞增殖率升高,淋巴細胞培養上清液中分泌的il 4和inf y也升高,且以il 4更明顯。
  2. This modification includes : ( 1 ) selecting two important molecules as candidates, ( 2 ) choosing a promiscuous t - cell epitope, and two b - cell epitopes or conserved amino acid sequences from the two important molecules, ( 3 ) connecting them adequately through analysis by the molecule designing software. therefore, the synthetic new antigen may interfere with the process of fertilization by multiple ways and its contraceptive effects may be enhancing. based on the molecule designing methods, the b - lymphocyte cell epitope of sperm / testis specific protein sp17 and cyritestin which interfere with fertilization in mouse, as well as the promiscuous th cell epitope of the ribonuclease ( rnase ) in bovine were selected

    本研究以蛋白質分子設計的理論和方法研究避孕疫苗,將sp17和cyritestin關鍵表位和牛核糖核酸酶非選擇性th細胞表位合理組合,獲得新抗原- 35肽序列;並在合成、純化後分別與弗氏佐劑、免疫刺激復合物( iscoms )混合后免疫不同遺傳背景的雌性小鼠,觀察血清和生殖道內的特異性抗體滴度的動態變化、生育力的改變以及免疫后小鼠重要臟器的組織病理學改變:以及在ivf下,新抗原的特異性抗血清對精卵相互作用的影響及抗原在精子表面的特異性定位。
  3. Detection of antigen - binding affinity of mg7 recombinant phage antibody elisa was repeated to confirm the antigen - binding affinity of positive clones screened out in the former procedure ; these positive phages were examined by restriction analysis ( ecor i and hind iii ) ; competitive elisa was performed to test the inhibitory ratio of these positive clones to the binding affinity of mg7mab and its relevant antigen, the positive dones possessing apparent inhibitory effect were singled out for later use

    X陽性克到駛知烘扳原kbbjg )濁對陽性克隆進行限制隴臥賜析( uwi和hedlll )鑒定三用競爭elisatoljmg7重組噬菌體抗體性克隆對mg7單扶與其相應抗原結合忙的喇率,從中j ) ed出對mg7單抗與期眩抗原結合有抑余j效應的克隆用於進一涉研究。
  4. Culture of mg7 hybridoma cells and detection of antigen - binding affinity of mg7 mab by elisa 2. construction and identification of mg7 recombinant phage antibody library mrna was isolated from cultured mg7 hybridoma cells and converted into cdna ; the variable fragments of heavy and light chain were separately amplified and assembled into scfvs with a specially constructed dna linker by pcr. the scfvs dma was ligated into the phagmid vector pcantabse and the ligated sample was transfered into competent e. co / / tg1 to generate a bacterial form of mg7recombinant phage antibody library ; volume and recombinant ratio of the library were evaluated by means of bacterial colony counts and restriction analysis ( ecor i and hind iii )

    Mg _ 7重組噬菌體抗體庫的構建及鑒定從培養的mg _ 7雜交瘤細胞中提取並分離mrna ,反轉錄成cdna ;利用pcr分別擴增mg _ 7單抗的重鏈及輕鏈可變區基因,並通過? dna連接子將二者連接起來形成mg _ 7單鏈抗體基因;將mg _ 7單鏈抗體基因插入pcantab5e ;將連接產物轉化感受態tg1大腸桿菌,制備細菌形式的mg _ 7重組噬菌體抗體庫;通過菌落計數和限制性酶切分析( ecor和hind )評估mg _ 7重組噬菌體抗體庫的容量和重組率。
  5. Western - blot analysis showed the expressed protein was specific to antisera against prv fa strain. the ge - elisa for differentiation of prv infected from vaccination was developed using the expressed ge protein as antigen

    Coli中高效表達的偽狂犬病病毒ge蛋白為抗原,以辣根過氧化物酶( hrp )標記的spa為二抗,建立了ge - elisa鑒別診斷方法。
  6. Quantitative analysis of special literature on antigen cd

    44專題文獻計量分析
  7. Second, a prokaryotic expression construct, obtained from invitrogen transformed into prokaryotic and induced to express vp1 protein. the expressed vp1 fusion protein was purified by affinity chromatography using glutathione - agarose resin and used in elisa and western bolt analysis as the antigen. the elisa and western blot results showed that the anti - fmdv antibody was elicited specifically against vp1 antigen

    第二,為了得到抗原蛋白,將vp1的原核表達質粒pgex - 4t - vp1轉化入大腸桿菌bl21中,經iptg誘導,裂解細胞後用瓊脂糖珠進行純化,用elisa和westernblot進行檢測,結果表明誘導表達出所需大小的融合蛋白。
  8. Constructed the fusion protein expression vector of echistatin, . and identify it by dna sequencing. the vector can express echistatin fusion protein at a high level, the fusion protein molecular weight is about 16000 da in sds - page analysis, and the fusion protein consists more than 30 % of total protein, the fusion protein has specific antigen - antibody reaction with rabbit anti - echistatin polyclonal antibody. the fusion protein include : hpk5. his + 6tag, and echistatin. echistatin can be released by cnbr cleavage

    構建了echistatin融合蛋白表達載體,經dna測序鑒定正確后,溫控誘導表達,獲得了高效表達,表達產物經505一隊ge分析,分子量為16000oa ,符合預計的融合蛋白分子量,表達產物. ll 』菌體總蛋白的30 %以上, westem一blotting結果顯示,該日的蛋白能夠和echistatin多克隆抗體發生特異性抗原抗體反應,表明我們成功構建了eohistatin的高效融合表達克隆。
  9. Burg jl, perelman d, kasper lh, et al. molecular analysis of the gene encoding the major surface antigen fo toxoplasma gondii j. j immunol, 1988, 141 : 3584

    陳曉光,江靜波.應用聚合酶鏈反應技術建立弓形蟲表面抗原基因的克隆與測定j .中國寄生蟲學與寄生蟲病雜志, 1994 , 12 ( 2 ) : 129
  10. The elisa and western blot analysis indicated that the reaction between annserum and antigen was high specifically. to block the annfaf expression in strawbern. " fruit, the antisense gene of annfaf

    為獲得annfaf基因的表達缺陷型植株,以研究該基因在草莓果實成熟過程中的調控作用,本研究構建了annfaf反義融合基因的植物重組表達質粒prok - annfaf 。
  11. An analysis on detecting rate of hbv antigen in the personnel engaged food trade and its countermeasure of prevention and cure in tanggu district

    天津市塘沽地區食品從業人員乙肝抗原檢出率分析及防治對策
  12. 2. in this thesis, the fractai reaction kinetics analysis was first to use in the study of heterogeneous reactions happened on the surf8ce of piezoelectric sensor the adsorption kinetic modei of antibody and the immunoreaction kinetic modei of antibody binding antigen on the surf8ce of piezoeiectric sensor were set up. when the models were appiied to the experimentai, good fitting results were obtained

    本文首次利用分形反應動力學理論來研究壓電生物傳感器表面發生的不均一反應並對生物大分子抗體吸附到傳感器敏感膜表面,以及發生在敏感膜表面的抗原抗體反應進行初步研究;提出了在壓電石英晶體表面發生的大分子吸附反應或抗原抗體反應的動力學反應模型;對實驗進行了應用,獲得了較好的擬合結果,驗證了模型。
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