兔血清白蛋白 的英文怎麼說

中文拼音 [tùxiěqīngbáidànbái]
兔血清白蛋白 英文
albumin rabbit serum
  • 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...
  • 白 : Ⅰ形容詞1 （似雪的顏色） white 2 （清楚; 明白; 弄明白） clear 3 （空的; 沒加他物的） pure; clear; ...
  • 蛋 : 名詞1. （鳥類或龜、蛇類所產的卵） egg 2. （像蛋形的東西） an egg-shaped thing 3. （辱罵之詞）
  • 清白 : pure; clean; unsullied; have clean hands; stainless
  • 蛋白 : 1. （卵中透明的膠狀物質） egg white; albumen; gary2. [生物化學] （蛋白質） protein
  1. The second part, a renewable piezoelectric immunosensor is developed for the antibody of schistosoma - japonicum ( sjab ). after incubating 32 kd molecular antigens of schistosoma japonicum ( sjag ) on the qcm by applying the immobilization above, the nonspecific sites on the immunosensor are sealed by using bsa and nrs together. the immunosensor can detect the sjab with the linear range of 0. 54 ~ 32. 50 ug / ml

    以感染兔血清為檢測對象，採用聚電解質吸附固定法，將日本血吸蟲分子抗原（ siag32kd ）固定於石英晶振表面，再以牛血清白蛋白（ bsa ）和正常兔血清（ nrs ）聯合封閉晶振上非特異性活性位點，可在0 . 54 32 . 50ug ml范圍內檢測感染兔血清中日本血吸蟲抗體。
  2. The protein - storing cells in swietenia macrophylla were found to be populus - type, i. e. ordinary parenchyma cells containing both vacuolar protein inclusions and starch grains

    用21kda蛋白質的抗血清進行兔疫印跡分析表明， 18kda蛋白質和21kda蛋白質有相同的抗原決定簇。
  3. After the recombinant plasmid pcdna3. 1 / ts87 was identified by digestion of hindlll and bamh i, it transformed into cos7 by lipofectamine. expression product was identified by immunohistochemical method, sds - page and western - blot. the immunocytochemistry result has shown that specific brown - staining grains were found in the cytoplasm of cells transformed by recombinant plasmid versus not seen in cells transformed by pcdna3. 1 or normal cells ; the sds - page result has revealed that a band about 3 8kb was found in cell lysis transformed by recombinant plasmid versus not in cells transformed by pcdnas. l or normal cells ; the western - blot result has showed that only the band about 38kd was recognized by sera from rabbit infected by t. s artificially and sera from rabbit immunized with soluble antigen of t. s and with protein expressed by ts87 gene and by a monoclonal antibody of t. s

    通過細胞的免疫組化，細胞裂解物的sds - page電泳， westem - blot分析檢測目的基因的表達情況。免疫組化結果顯示：重組質粒轉染的細胞質中有棕褐色顆粒，而空載體轉染細胞及正常細胞無此現象；細胞裂解物sds - page電泳結果顯示：只有重組質粒轉染的細胞在約38kd處有明顯的蛋白帶，這與理論計算的ts87基因表達蛋白的分子量為38kd基本一致； western - blot分析結果顯示：約38kd的蛋白帶能夠分別被旋毛蟲感染兔血清，成蟲蟲體可溶性抗原免疫兔血清， ts87基因原核表達蛋白免疫兔血清（ ts87血清）以及一株具保護性的旋毛蟲單抗特異識別。
  4. Anti - melatonin monoclonal antibodies of higher titer, affinity and good sensitivity were obtained by coupling mt to bovine serum albumin with formaldehyde and by immunizing mice with multifocal intra - dermal injections. we obtained 6 strains of hybridoma, all of them secreting specific antibodies to mt, we apply antibodies to determinate free mt inhuman serun with group - selective immunoassay technique. an inhibition curve for mt was obtained in the range of 50pg to30ng, and 1. 4ng of mt inhibited the value of the assay by half. we evaluate the specificity of antibodies by determination of cross - reactivity of several analogues, the moabs recognized mt but

    通過將mt用甲醛作連結劑連結到牛血清白蛋白上sa採用皮下多點注射兔疫小鼠得到了高效價，高親和力，較好特異性的抗mt單克隆抗體，最後獲得了5株單克隆細胞株，都能分泌針對mt的特異性抗體，建立了選擇性基團免疫分析法，用制備的抗體測定了人血清中mt的含量，作了mt的抑制標準曲線，其抑制范圍從50pg ? 30ng ，半抑制量為1
  5. Thin sections of host leaf cells infected by bbwv - 2 isolate b935, which were gold - labeled by antibodies of bbwv - 2 coat protein ( cp ) and vp37, respectively, were prepared to elucidate the locations of vp37 in cell and possible function of vp37 and cp in cell to cell movement. observation in electron microscope showed that virus particles were presented not only in cytoplasma but also in chloroplast, while vp37 was existed only in cytoplasma and associated with tubular structure through the cell wall

    為研究vp37在寄主細胞中的作用機制及其在細胞中的分佈，通過膠體金間接標記6his - vp37兔抗血清，同時還標記了病毒的外殼蛋白單克隆抗體，對bbwv - 2分離物b935感染的病葉超薄切片的電子顯微鏡觀察發現：病毒粒子除了聚集在胞質中，還存在於寄主的葉綠體內； vp37蛋白能在細胞壁上形成管狀結構，在胞質中亦有分佈。
  6. In this paper, the pea ferritin was purified from pea seed, and its antiserum was raised from rabbits for investigating the expression of transgenic plant. the main experimental results were summarized as following : 1. establishment of ferritin detection system

    本論文開展了豌豆鐵蛋白的純化、免疫家兔制備豌豆鐵蛋白抗血清以及植物鐵蛋白免疫學檢測等一系列的研究，現將主要研究內容和結果總結如下： 1 、鐵蛋白檢測系統的建立純化過程中以鄰菲咯啉顯色法檢測鐵蛋白，具有簡單、靈敏、直觀等優點。
  7. Under the conditions of sds - page, it depolymerized into only one subunit of 28 kd, which reveal that the subunit of purified ferritin of pea is undivided 4. preparation of antiserum of pea ferritin the purified pea ferritin was mixed with freund ' s complete adjuvant or freund ' s incomplete adjuvant, and then administered through palmula, back, abdominal cavity, vena auricularis and other routes for rabbits. seven weeks later, the litre of antiserum reached 1 i 32

    4 、免疫家兔制備豌豆鐵蛋白抗血清民二功尋咬徑b一侖一以純化的豌豆鐵蛋白作為抗原，並分別加入弗氏完全佐劑和弗氏不完全佐劑等兔疫家兔，經過足掌、背部皮下、腹腔和耳靜脈等途徑進行免疫， 7周后獲得效價高達1 ： 32以上的豌豆鐵蛋白抗血清。
  8. Table 1 serum lipids in rabbits at before treatment, 4th and 8th week ( s, n = 8, mmol / l )

    表1 .兔血清總膽固醇、甘油三酯和高密度脂蛋白膽固醇水平
  9. The expression conditions of e2 gene in p. pastoris were optimized, the results indicated that the peak obtained after 72 hours ; pattern of inhibition / induction could improve expression level ; the best ph value were between 7. 5 and 8. 0 and the optimized methanol - induced concentration was 2 % - 3 % the e2 genes of the prevalent strain ( guangxi yulin strain ) and c strain derived from rabbit spleen tissue were amplified and cloned into e. coli the expression vector pproex - htb respectively, the recombinant plasmids pproex - gxyl and pproex - c were obtained and then were transformed into the dh5a e. coli competent bacteria respectively, the recombinant bacteria could express the major antigen region of e2 gene, the expression yields amount to 35 % and 38 % repectively

    豬瘟病毒ez基因的原核表達： pcr擴增出當前豬瘟流行野毒株，中國豬瘟兔化弱毒（ c株）兔脾組織毒ez基因的主要抗原區，將其克隆到原核大腸桿菌表達載體pproex htb中誘導表達，經sds page檢測表明，重組質粒能表達ez基因主要區蛋白， westernblot檢測表明，誘導表達蛋白與豬瘟陽性血清發生特異性反應，表達量為35和38 ，可用於基因工程診斷抗原。
  10. Then protein crystal of eif - 5a was observed using atomic force microscopy. further, the polyclonal and monoclonal antibodies were gained from immunized rabbits and rats. hypusine - contained eif - 5a plays a role in cell growth and differentiation

    用得到的重組蛋白分別免疫家兔和小鼠，獲得兔的抗血清和三株持續分泌單抗的雜交瘤細胞株，為進一步分析eif - 5a的功能提供了檢測手段。
  11. These indicated that the porcine il - 6 gene was correctly transcribed and translated in the recombinant bacteria. the fusion protein was recovered from polyacrylamid gel and used to immunize the rabbit, and the liter of rabbit anti - porcine il - 6 serum from immunized rabbit was 1 : 128, 000

    從制備性聚丙烯酰胺凝膠中回收融合蛋白，用mtt法測定重組蛋白刺激小鼠脾淋巴母細胞增殖反應活性，並以重組蛋白免疫家兔制備抗豬il - 6滴度為128 ， 000的高免兔血清。
  12. Determination of the unbound clozapine concentration in human serum albumin ( has ), human plasma, rabbit serum and plasma samples by capillary electrophoresis in the frontal analysis mode ( ce / fa ) was developed

    摘要採用毛細管電泳-迎頭分析模式體外實驗測定了人血清白蛋白溶液、人血漿、兔血清和血漿樣品溶汲中游離氯氮平的濃度。
  13. The high titer specific ndrg2 antibody is indispensable to reseach deeply the functions or the tissue and subcellular distribution features of ndrg2, ha order to prepare ndrg2 antibody, the whole ndrgl sequence was cloned into prset - a vector and two truncated sequences of ndrg2 were cloned into pgex - 4t - l vector. after induced by iptg, the fusion proteins were expressed in e. coli ; rabbits immunized with the whole length ndrg2 protein were reinforced with two shortened fragments of ndrg2 ; after immunization, rabbits produced high titer antiserum against ndrg2. then antisemm was absorbed using ndrg2 antigen immobilized on nc filters, the purified product of antiserum shows high special to ndrg2 protein, and the separated inclusion body of 6his - ndrg2 will be useful for the further reseach

    為制備高效價的ndrgz抗體，分別構建了prset a雌、 pgex4t d唾倉和pgex4tl七三種原核重組表達質粒，並在大腸桿菌中誘導表達出相應的融合蛋白；用全長gstjqdrgz蛋白免疫兔，然後用gst ndrgz人和gstjqdrgze片段加強免疫，經免疫得到了較高效價的兔抗人ndrz多克隆抗血清，利用固定於硝酸纖維素膜上的ndrgz抗原親和吸附純化抗血清，提高了ndrgz抗體的特異性；並對包涵體形式表達的6his ndrgz進行初步的分離純化。
  14. By immunizing rabbits with aa 192 - 326 fragment, polyclonal sera were obtained that were able to recognize e1 proteins expressed in both e. coli and mammalian cells, suggesting that e. coli - derived e2 proteins carried hcv e1 - specific, glycosylation - and - conformation - independent epitopes

    利用aa192 - 326免疫家兔，獲得了可識別大腸桿菌和哺乳動物細胞表達之e1蛋白的多抗血清，表明大腸桿菌系統表達的e1蛋白攜帶有hcve1特異的、不依賴于糖化和立體構象的抗原決定簇。
  15. The rabbits were haintmed with purified recombinant protein and the sera were examined for anti - tgev neutralwi astivity on the continuous porcine ibrs2 cells. the result showed that neutraldrig activity was 1 : 22. therefore, the neuthelizing activity of anti n protein antibody against infectious tgev in vitro was very iow from the result of neutra1hation ( vn ) test

    將純化的融合蛋白免疫家兔，制備的抗血清在豬ibrs _ 2傳代細胞上進行中和實驗，結果顯示中和效價為1 ： 22 ，表明n蛋白所產生的抗體對tgev的中和活性較低。
  16. The recombinant p22 proteins were purified effectively by probond ? resin. 3

    Western - blot證實重組蛋白能被感染弓形蟲兔血清所識別。
  17. 3. preparation of polyclonal antiserum against angiotensinogen in order to study agt in protein level and also for other continuing work, the c - teminus of rat angiotensinogen was expressed in e. coll. rabbits were immunized by this expressed 6his - agtc protein and serum from different rabbits were raised

    血管緊張素原多克隆抗血清的制備為研究agt蛋白表達及后續工作，在大腸稈菌中融合表達了agt蛋白的c末端，以此融合蛋白為抗原免疫家兔，制備抗血清。
分享友人
分享到 Line

分享到臉書