噬菌體抗體庫 的英文怎麼說

中文拼音 [shìjūnkàng]
噬菌體抗體庫 英文
phage antibody library
  • : 菌名詞1. (蕈) mushroom2. (姓氏) a surname
  • : 體構詞成分。
  • : Ⅰ動詞1 (抵抗; 抵擋) resist; combat; fight 2 (拒絕; 抗拒) refuse; defy 3 (對等) contend with...
  1. The monoclonal antibodies ( mab ) specific for the nucleoprotein of prrsv were used to select a phage random heptapeptide library

    採用隨機7肽對單克隆ge3識別的原表位進行了鑒定。
  2. The murine phage antibody library was amplified and then panned by human chorionic gonadotropin for four rounds. the last round enriched phage clones were used to reinfect

    由鼠源噬菌體抗體庫淘選到展示有人絨毛膜促性腺激素單鏈克隆。
  3. 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單鏈基因;將mg _ 7單鏈基因插入pcantab5e ;將連接產物轉化感受態tg1大腸桿,制備細形式的mg _ 7重組噬菌體抗體庫;通過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。
  4. Phage display describes a selection technique in which a peptide or protein is expressed as a fussion with a coat protein of bacteriophage, resulting in display of the fused protein on the surface of the virion, while the dna encoding the fussion resides within the virion

    自1985年gpsmith首次提出展示技術以來,隨著生物技術的發展,隨機肽已成為研究分子間相互作用的有力工具,特別是在原表位研究方面。
  5. In this experiment, to screen the epitope of e2 protein of classical swine fever virus ( csfv ) defined by the monoclonal antibody ( mcab ) all, which had been prepared in previous experiment, the mcab all was raised in mice and followed by purification, the concentration of protein was assayed by using the bca protein assay kit

    本室利用e2基因疫苗制備了多株單,為e2的原表位研究提供了條件,我們以隨機12肽分析鑒定了豬瘟病毒e2蛋白的原表位,為深入研究豬瘟病毒的原結構、制備更有效的診斷試劑和疫苗提供更多理論依據。
  6. In the present study, the express library of monoclonal anti - sp18 scfv ( single chain fragment variable ) gene is constructed and selected for further study of sp18 antigen on mammalian fertilization and embryogenesis. total rna were firstly isolated from these growing hybridoma cells which secretes monoclonal anti - sp18 antibodies. after obtained using rpas system, vh and vl genes were used to assemble scfv gene fragment with a linker primer

    應用重組噬菌體抗體庫技術,從分泌小鼠牛精子sp18的雜交瘤細胞系中分離總rna ,克隆重鏈和輕鏈可變區基因,加入連接肽引物( linkerprimer )組裝成單鏈scfv ( singlechainfragmentvariable )基因並用rs引物進行擴增, sfi 、 not酶切,回收后與pcantab5e載相連,轉化e . colitg1宿主,構建單鏈
  7. Selection of anti - hcg scfv from murine phage antibody library selection of anti - hcg scfv from murine phage antibody library

    噬菌體抗體庫中淘選人絨毛膜促性腺激素的單鏈
  8. The phagemid particles displaying functional scfvs were rescued by reinfection of helper phage m13ko7, thus a murine antibody library was obtained

    經輔助m13ko7超感染回收全部重組,此即噬菌體抗體庫
  9. Methods : a set of oligonucleotide primers were designed and used to amplify the vh and vl gene from anti - hbsag fab antibodies screened from phage antibody library. the products were cloned into puc19 vector and their sequences were analysed. the vh and vl gene fragments were tethered by a peptide linker and a leader sequence coding region, with the leader sequence added at 5 " terminus of each gene ( l - vh - linker - vl ) and designated as l - scfv

    方法以從噬菌體抗體庫中篩選獲得的hbsag的fab基因為模板,分別擴增出其輕、重鏈可變區( v _ l 、 v _ h )基因,通過重組pcr方法將輕、重鏈可變區基因用連接肽( gly _ 4ser ) _ 3的編碼序列連接,並引入前導肽編碼序列,構建具有l - v _ h - linker - v _ l結構的單鏈基因。
  10. Construction of murine phage antibody library and selection of n - peptide - binding single - chain antibodies

    小鼠噬菌體抗體庫的構建和n -肽結合單鏈的篩選
  11. In the present paper the application of dna library, phage display random peptide library, phage antibody library, etc. in the research of serodiagnostic reagents and their special values were reviewed

    本文綜述了基因文展示肽噬菌體抗體庫技術在血清學診斷試劑研製中的應用及其各自的優點。
  12. The patterns of sds - page indicated more than 30 % of recombinant proteins could be obtained from the extract of e. coli bl21. furthermore, library of recombinant phage antibodies was constructed from total rna isolated from spleen of the female balb / c mice immunized by bull sperm

    首先用牛精子免疫雌性四周齡balb c小鼠,從其脾臟組織分離總rna ,應用重組噬菌體抗體庫技術,構建了一個針對牛精子的
  13. Panning and enrichment ofmg7 recombinant phage antibody the transformed cells were infected with m13k07 helper phage to produce a phage form of mgy recombinant phage antibody library ; after three rounds panning of the library with the mgrbinding antigen highly expressed gastric cancer cell line kato iii, the mg7 scfv displayed phage dones were selected from the enriched recombinant phages by elisa

    3 mg _ 7重組噬菌體抗體庫的淘篩用m13ko7輔助感染轉化,以挽救出形式的;用高表達mg _ 7原的胃癌細胞系kato對進行三輪淘篩;用elisa篩檢呈現有mg _ 7scfv的單克隆。
  14. Part ii screening of tnfa mimotopes from phage display peptide library : based on the results of screening tnfa binding - peptides, we have tried to use neutral tnfa mcab j1d9 as target to screen tnfa mimotopes from c7c phage display peptide library, which may be another form of antagonist for tnfa, and the mimotopes were identified by sandwich elisa. after 3 rounds of screening, we got 9 phage clones identified as positive clones which can bind with mcab j1d9. we also identified the binding between mimotopes and tnf receptor by competitive elisa, and the results showed strongly binding. the amino acid sequence results shown three different sequences : c - rrpaqsg - c - nkhnrki - c and c - rgmsrki - c

    在對環七肽進行三輪親和性篩選后,隨機挑選20個克隆, elisa鑒定出9個陽性克隆,經dna測序推出三種氨基酸序列: c - rrpaqsg - c 、 c - nkhnrki - c和c - rgmsrki - c ,其中優勢克隆序列為c - rrpaqsg - c ;鑒定結果顯示陽性克隆能夠與tnf受結合,並且能夠阻斷tnf與受的結合,提示篩選得到的環七肽克隆展示肽具有tnf的原性及與tnf受結第一軍醫大學顧士學位論文合的特性,為tnfa表位模擬肽。
  15. Our research can be divided into the following four parts : part i screening of tnfa - binding peptide from phage display peptide library : the tnfa binding - peptides were screened from c7c phage display peptide library by using rhtnfa as target protein and identified by sandwich elisa, for exploring whether the binding - peptides can be used as antagonist of tnfa or not

    篩選tnf小分子模擬肽及結合肽對于tnf研究具有重要的意義。本研究包括以下四個方面: 1 、 tnf結合肽的研究:以rhtnf為靶對環七肽進行篩選,以尋求可拮tnf活性的小分子短肽。
  16. The antibody induced by peptide gwyydal abolished vegf - induced huvec growth in dose dependent which specifically express the kdr. moreover, both of the peptide gwyydal and vasavfysalve displaying on phage also inhibited the growth of huvec

    [結論]從中篩選到了與有高親和力的陽性克隆,表達的7 、 12肽gwyydal 、 vasavfysalve模擬了vegf的原表位,引起顯著的- vegf反應。
  17. Identification of epitope recognized by monoclonal antibody with phage - displayed random peptide library

    隨機肽在確定單識別表位中的應用
  18. These phage display peptides may be the tnfa mimotopes. part iii specific c7c tnfa mimotope phage clone as target for screening of tnfa specific binding - peptides from 12mer phage display peptide library : by using the specific c7c tnfa mimotope as target, we developed a novel approach for screening phage peptide library targeting specific phage display peptides. we used c7c tnfa mimotope phage clone lcs - 7 ( c - rrpaqsg - c ) as target to screen 12mer phage peptide library and identify the positive clones by phage elisa

    3 、以特異性克隆為靶篩選肽的研究? ?一種肽篩選新方法的建立:為了深入研究細胞因於與配基(受)相互作用的關鍵殘基及其空間構象,在上述研究基礎上,我們以tnfa表位模擬肽克隆為靶篩選十二肽,找尋與之結合的tnfa結合肽克隆;並以此拓寬了的應用范圍。
  19. Screening antigenic epitopes from hcv core protein random peptide libraries displayed on phage

    核心蛋白隨機展示肽中篩選原表位
  20. Independent clones was constructed and affinity panning of anti - n - peptide antibody fragments was carried out

    的小鼠噬菌體抗體庫,並從中淘選出對n -肽有結合活性的單鏈
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