特異反應原 的英文怎麼說

中文拼音 [tèyìfǎnyīngyuán]
特異反應原 英文
idiotoxin
  • 特 : Ⅰ形容詞（特殊; 超出一般） particular; special; exceptional; unusual Ⅱ副詞1 （特別） especially; v...
  • 異 : 形容詞1 （有分別; 不相同） different 2 （奇異; 特別） strange; unusual; extraordinary 3 （另外的;...
  • 反 : Ⅰ名詞1 （方向相背） reverse side 2 （造反） rebellion 3 （指反革命、反動派） counterrevolutionari...
  • 應 : 應動詞1 （回答） answer; respond to; echo 2 （滿足要求） comply with; grant 3 （順應; 適應） suit...
  • 原 : Ⅰ形容詞1 （最初的; 原來的） primary; original; former 2 （沒有加工的） unprocessed; raw Ⅱ動詞（原...
  • 特異 : 1 （特別優異） exceptionally good; excellent; superfine2 （特殊） peculiar; distinctive特異功能 s...
  1. It has been demonstrated that complement activating and cr2 cross - linking on b lymphocytes set up a bridge between innate and acquired immunity. the interaction of c3 and cd21 on b lymphocytes will benefit initiating immune response and regulating primary antibody response. cd21 / cd35 is important in the process of antibody avidity maturing, this is critical to b lymphocyte activation especially in the state of low antigen concentration

    現己證實補體的活化以及b細胞表面crz的交聯在先天和獲得性免疫之間架起了重要的橋梁，表現為c3與b細胞cdzi的相互作用有利於啟動抗體應答反應，並對初級抗體應答反應有調節作用： cdzi cd35對于抗體的親和性成熟具有重要作用，在抗原濃度低的情況下，對于活化b細胞是至關重要的，而且mlgm （交聯有利於特異的低親和性b細胞對t細胞依賴性抗原和t細胞非依賴性抗原產生免疫應答。
  2. The high specificity of the dot - ppa - elisa was confirmed by specific blocking test and also by cross - reaction test. the diaphragm did not react with the antibodies against salmonellosis, streptococcosis, colibacillosis, chlamydiosis, hcv, ppv, prv, brucellosis. erysipelas, suis and chlamydiosis in cross - reaction test. the diaphragm has good sensitivity and could detect some pasteurella - positive test serum which has been diluted to2 - "

    試驗證明所建立的dot - ppa - elisa具有較好的特異性，與豬瘟、仔豬副傷寒、豬丹毒、豬細小病毒病、豬偽狂犬、豬布氏桿菌病、豬衣原體病陽性血清無交叉反應。
  3. Study on immunoreaction induced by dcs loaded with hepatocarcinoma antigen peptide in vitro

    樹突狀細胞負載肝癌抗原肽疫苗體外誘導特異性免疫學反應的研究
  4. It still remains a question whether the rearrangements of igh come from h / rs cell or the background lymphocytes. in this study, we have detected the igh clonal correlation between the h / rs cells and the background cells, from a new aspect to study the clonality of h / rs cell and its relation with the background cells. the expression of b - cell - specific activator protein ( bsap ) was detected in hl. igh gene rearrangements were analysed by the methods including gene analysis in neoplasms tissue and micropicked cells from paraffin - embedded sections, sequencing to test the pcr product, and in situ pcr

    本研究將在以往研究的基礎上，在國內率先把b細胞核反式作用因子? b細胞特異性激活蛋白（ b - cell - specificactivatorprotein ， bsap ）應用於hl的研究，檢測hl的bsap表達，並採用石蠟刮片組織和微切割單細胞的基因分析、測序分析和間接原位pcr等方法，同步觀察分析h rs和背景淋巴細胞的igh基因克隆相關性，從又一個新視角探究chl的腫瘤性h rs細胞克隆性及與背景淋巴細胞的關系。
  5. Lastly by using the technique of dot blot hybridization, the genome dna of chlamydia was detected with the probe of momp gene labeled with dig - 11 - dutp by using the way of random primer. the results showed the degree of sensitivity of the probe was 10 pg and other pathogens could not be detected by this probe. by comparing the diagnostic ways of nucleotide probe and fc, the technique of nucleotide probe were proved to have high sensitivity and speci fi city

    最後，用地高辛隨機引物法標記成momp基因核酸探針，斑點雜交檢測衣原體基因組dna ，靈敏度可達10pg ，且不能檢出其它病原體的核酸。將核酸探針法與補體結合反應法對衣原體感染的診斷進行比較，初步證明該探針具有較高的敏感性與較強的特異性。
  6. When the antigen ( brief named ag ) invaded into the organism, and the body can produce a kind of material ( high molecular weight protein, named antibody, brief named ab ) that can distinguish this antigen and evacuate it, the antigen and antibody take place the immuno - reaction. using their highly sensitivity to response mass change and specificity, it can be fabricated a piezoelectric immunnosensors

    當異種蛋白（稱為抗原， antigen ，簡稱ag ）侵入生物體內時，體內能產生識別此類異物並將其排出的物質（大分子量蛋白質，稱抗體antibody ，簡稱ab ） ，抗原與抗體發生免疫反應，利用抗體（或抗原）對抗原（或抗體）的特異性識別功能和壓電晶體的高靈敏質量響應可製成壓電免疫傳感器。
  7. 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。
  8. And the no - isothermal structure can accelerate the breaking of gravity wave in mesospause, and the breaking of gravity wave is an important source of convection and small - scale waves. the propagation of gravity wave will affect the distribution of minor species. the breaking of gravity wave accelerates the downward transport of atomic oxygen, some smaller - scale structures appear on the horizontal distribution of atomic oxygen number density, and other chemical species are also affected due to the chemical reaction with atomic oxygen and the propagation of gravity wave

    在重力波的傳播過程中，氫氧大氣成分的水平和垂直分佈均受到了不同程度的影響，以氧原子的響應最為明顯，而其中重力波破碎在氧原子水平分佈上的反應則是非線性重力波過程的一個重要表現；另外，分析顯示，重力波的非線性傳播對oh氣輝的峰值分佈由明顯影響，小尺度重力波的傳播有時會引起oh氣輝出現奇異的雙峰分佈，重力波的破碎現象也可以從對氣輝的觀測中反映應出來，這對利用氣輝觀測研究重力波傳播特性有非常重要的指示意義。
  9. The results from sds - page presented that there were three female specific protein subunits with molecular weights of 123 kd, 120 kd and 91 kd, respectively. we can conclude the higher molecular compose of two subunits ; the results from two dimension electrophoresis showed the isoelectric points of two female - specific spots with molecular weight of about 120kd were 5. 5 and 5. 7. immunodiffusion reactions demonstrated that vg existed both in female fat body and hemolymph, which as vn was deposited in the ovary, while not in the male

    Page電泳結果表明：麗蠅蛹集金小蜂明顯存在2條雌特異性帶-卵黃蛋白，分子量分別為181kd和136kd ； sds - page電泳分析：存在3條雌特異性帶，其分子量為123kd 、 120kd和91kd ，由此，可推定卵黃原蛋白（ vitellogenin ， vg ）和卵黃磷蛋白（ vitellin ， vn ）由2個蛋白組成，其中分子量較大的蛋白由2個亞基組成；雙向電泳結果顯示，在120kd附近有兩個特異性點，其等電點為5 . 5和5 . 7 ；雙擴散表明，麗蠅蛹集金小蜂卵黃磷蛋白的抗血清與雌隱成蟲蟲體、脂肪體、血淋巴和卵巢勻漿液均有免疫沉澱反應，而與雄蜂血淋巴無免疫反應，說明了vg與vn具有免疫同源性，是雌特異性蛋白，且由脂肪體合成。
  10. Western blot analysis demonstrates that it reacts positively with goat antibody

    Western - blot鑒定表達產物有特異的抗原抗體反應。
  11. Western - blotting result demonstrated rhpf4 had specific reaction with rabbit anti - hpf4 antibody

    Western blotting檢測表達產物與兔抗人hpf4抗體發生特異的抗原抗體反應。
  12. Backgroud : the activation of antigen - specific t cells plays a vital role in the initiation and development of some immune - related diseases, such as transplant rejection and allergic diseases

    背景：抗原特異性t細胞的活化在一些免疫相關疾病（如移植排斥反應、變應性疾病）的發生、發展中起著主導性的作用。
  13. The high specificity of dot - ppa - elisa was proved by the specific blocking test, and also by the cross - reaction test in which the diaphragm did n ' t react with the antibodies against pasteurellosis, streptococcosis, colibacillosis, chlamydiosis, hcv, ppv, brucellosis, prv and foot - mouth disease. the diaphragm has good sensitivity and could detect some salmonella - positive test serum which has been diluted to 1 : 2048. stored at 4 for at least 6 months or at 10 - 25 " c for 4 months, the sensitivity and specif icity of the diaphragm did n ' t change, so it has good stability

    本研究制備的診斷膜片特異性強：不與豬衣原體病、豬口蹄疫病、豬大腸桿菌病、豬布氏桿菌病、豬瘟、豬偽狂犬病、豬細小病毒病、豬巴氏桿菌病、豬鏈球菌病的陽性血清發生交叉反應；診斷膜片具有良好的敏感性，能夠檢測到1 ： 2048稀釋的動物試驗陽性血清；膜片的保存期長，在10 25可保存4個月、 4條件下至少可保存6個月其靈敏度不變。
  14. As well as in eukaryocyte ( hepg2 and cos - 7 ), then detect their antigenity as a basis study and explore of the choice of immunogen for preventive and therapeutic vaccines of hepatitis b. methods : the gene fragments coding 152aa ( si ) and 124aa ( s2 ) of the carboxyl terminus of hbsag were amplified by pcr from plasmid pecob6 with a pair of primers containing different endonuclease sites and were cloned into multiple cloning sites of plasmid pbks ( + )

    為乙型肝炎的預防和治療性疫苗免疫原的選擇進行初步的研究和探討。方法：本研究利用聚合酶鏈反應（ pcr ） ，通過設計帶有不同酶切位點的一對引物，從質粒pecob6特異性擴增hbsag蛋白羧基末端152個氨基酸（ s1 ）和124個氨基酸（ s2 ）的基因片段，分別將二者克隆到質粒pbks （ + ）的多克隆位點，篩選重組克隆。
  15. It delivers the false ? folding peptides for presentation to proteasomes in normal cells, while in tumor cells it acts as main tumor - resistant antigen, inducing specific immune response. recent research found that grp94 also relates with cell cycles, differentiation and apoptosis

    此外發現它還具有抗原提呈作用，在正常細胞中參與折疊錯誤蛋白到蛋白酶體的提呈；在腫瘤細胞中作為主要的腫瘤排斥抗原，引發針對該腫瘤細胞的特異性免疫反應。
  16. Purpose 1 construction of prokaryotic high expression vector of human platelet factor 4 ( h pf4 ) 2 expression and purification of r h pf4 3 bioassay of r h pf4 methods according to the modulation character of eukaryotic protein expression in prokaryotic cells, we design a pair of particular primers, and construct a prokaryotic expression vector pbv220 - r hpf4 by dna polymerase chain reaction ( pcr ) and dna recombinant technic. the expression plasmid was identified with pcr and dna sequencing. pbv220 - r hpf4 was transformed into e. coli dh5a, bl21 ( de3 ) and induced by increasing the temperature to 42. we identified the expression protein by sds - page and western - blotting

    目的1人血小板因子4 （ hpf4 ）原核高效表達克隆的構建2重組hpf4的表達及分離、純化工藝研究3重組hpf4的特性研究方法根據原核細胞表達真核蛋白的基因表達調控特點，設計合成一對特異引物，在pt7 - 7 - rpf4表達質粒的基礎上，應用聚合酶鏈式反應（ pcr ）對其cdna進行改造，通過dna重組技術構建成重組hpf4原核表達質粒pbv220 - rhpf4 ，用快速pcr檢測法、 dna測序分析，鑒定重組hpf4表達質粒的正確性。
  17. Piezoelectric sensing technique has been applied to many fields, including analytical chemistry, life science, environmental monitoring and surface sciences because of it ' s small size, high sensitivity, simplicity, low power consumption and broad sensing spectrum. piezoelectric immunosensors possess high selectivity provided by antibodies or antigens and sensitivity response directly to the mass change of proteins. immobilization technologies of biomolecules are of paramount importance in order to preserve their biological activity

    壓電免疫傳感技術利用壓電晶體與抗原抗體特異性免疫反應結合的特徵，通常在壓電石英晶體表面先固定抗原（抗體） ，響應溶液中抗體（抗原）引起的質量、密度和粘度等性質的變化，它兼具有壓電質量響應的高靈敏性和生物化學反應的高特異性。
  18. 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。
  19. The expressed products were purified by metal ( ni2 + ) chelation affinity chromatography and tested by western - blot. the results showed that his - tagged vp6 fusion proteins have a positive reaction with anti - jl94 serum

    採用western - blot對表達產物及純化產物進行反應原性分析，結果表明所得his - taggedvp6融合蛋白具有較好的抗原反應特異性。
  20. 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。
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