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抗兔
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  anti-rabbit
     The immunoglobulin of sheep anti-rabbit IgG was labelled with 6 [N-(4-aminobutyl)-N-ethyl]-amino-2, 3-dihydrophthalazine 1,4-dione (AB-EI) and taken as the second antibody.
     用6[N-(4-氨基丁基)-N一乙基]-氨基-2,3-二氢吩噻嗪1,4-二酮(ABEI)标记羊抗兔IgG免疫球蛋白作为第二抗体,第一抗体是兔抗人CRP。
短句来源
     A Antibody sandwich enzyme linked immunosorbent assay (ELISA) was developed for the detection of EDS-76 virus by employing the three kinds of IgG The optimal dilutions of chicken anti-EDS-76 virus, rabbit anti-EDS-76 virus and HRP-sheep anti-rabbit were 1:160, 1:300 and 1:1000, respectively.
     用鸡抗EDS-76病毒、兔抗EDS-76病毒和羊抗兔三种特异性高免血清IgG,建立了双夹心酶联免疫吸附试验(Eenzyme-linked immunosorbent assay ELISA)检测法,试验确定的鸡抗EDS-76病毒、兔抗EDS-76病毒和HRP-羊抗兔抗体的最佳工作浓度分别为1:160、1:300和1:1000。
短句来源
     The HF13504 of Millipore corporation were used to prepare the test strip, in which the sheep anti-rabbit IgG coated at 0.25mg/mL as control line, the polycolne antibody coated at 0.2mg/mL as the test line.
     通过比较选用Millipore公司的HF13504作为层析用膜,质控线采用二抗(羊抗兔)浓度为0.25mg/mL,检测线为纯化的多克隆抗体浓度均为0.2mg/mL;
短句来源
     The reference DNA probes were detected by mouse anti-digoxigenin, rabbit anti-mouseantibody-TRITC, and sheep anti-rabbit antibody-TRITC.
     标记地高辛的 DNA 探针用鼠源抗地高辛抗体(anti-Dig)、兔抗鼠抗体-罗丹明(TRITC)和羊抗兔抗体-TRITC检测。
短句来源
     The amount of anti-T-2 antibody bound to the plate was determined by reaction with goat anti-rabbit IgG-HRP and by subsequent reaction with the substrate.
     T-2抗体结合量用酶(HRP)标羊抗兔 IgG 与酶底物反应进行测定。
短句来源
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  anti rabbit
     Results: The positive percentages of anti sheep,anti horse, anti pig,anti rabbit,anti mouse and anti cattle Ig antibodies were 2.0%,2.4%,2.8%,0.8%,2.6% and 1.2%, respectively in 500 normal subjects;
     结果 :5 0 0名健康体检者血清中抗绵羊、抗马、抗猪、抗兔、抗小鼠、抗牛Ig抗体阳性率分别为 2 .0 %、2 .4 %、2 .8%、0 .8%、2 .6 %和 1.2 % ;
短句来源
     A magnetic particle second antibody (MSA I) was prepared by means of immobilizing donkey anti rabbit antiserum on Fe 3O 4 particles 10.8 nm±34% in diameter.
     以直径10.8nm±34%的Fe3O4粒子作磁性载体,物理吸附驴抗兔抗血清制备了磁性粒子第二抗体(MSA-I)。
短句来源
     A goat anti mice IgG- Eu~(3+) conjugate and goat anti rabbit IgG- Eu~(3+) were prepared by DTTA method .
     采用DTTA法,制备了Eu~(3+)-羊抗兔抗体和Eu~(3+)-羊抗鼠抗体。
短句来源
     The assay used UDSA-cLH-K-3 as reference standard, UDSA-cLH-I-3 as radio labelled ligand, rabbit anti-chicken LH(UDSA-AcLH-5) as first antibody, and donkey anti rabbit antiserum as second antibody.
     所用LH参照标准为USDA-cLH-K-3,碘化标记LH为USDA-cLH-I-3,第一抗体为兔抗鸡LH(USDA-AcLH-5),第二抗体为驴抗兔血清。
短句来源
     An indirect sandwich enzyme linked immunosorbent assay (IS ELISA) was described for detecting the viral antigens in the oral cavity or/and cloaca of NDV infected chicken by using the antibody (5μg/mL) of SPF chicken against NDV as captor,the antiserum (1∶200~600) of rabbit anti purified NDV reproduced with Vero cell as the second antibody,and the goat anti rabbit IgG (1∶5000) conjugated with peroxidase as indicator.
     以SPF鸡抗新城疫病毒(NDV)IgG为包被抗体(5μg/mL),兔抗NDVVero细胞培养纯化毒IgG为第二抗体(1∶200~600),酶标记羊抗兔IgG(1∶5000)为指示抗体建立间接夹心ELISA,检测实验免疫鸡、攻毒鸡及现地免疫鸡口腔或泄殖腔外分泌物。
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  “抗兔”译为未确定词的双语例句
     Therapeutic effect of 6-[4-(4′-pyridyl) aminophenyl]-4,5-dihydro-3(2H)-pyridazinone on hemorrhagic shock and its mechanisms in rabbits and rats
     6-[4-(4′-吡啶)氨基苯]-4,5-二氢-3(2H)哒嗪酮抗兔和大鼠失血性休克效应及初步机理
短句来源
     4 immunopositive plaques (DPF-1.1, DPF-1.2, DPF-1.3 and DPF-1.4) were purified.
     以制备的豚鼠抗兔DPF-1(64 kDa)多克隆抗体克隆筛选到4个免疫阳性重组体(DPF-1.1、DPF-1.2、DPF-1.3和DPF-1.4),并被纯化。
短句来源
     5th,Dripted antibody of BDNF(1:100)、Bcl-2(1:100)、Bax(1:100)on samples respectively and incubated for allnight in wet box.
     (5)分别用一抗兔抗鼠的BDNF(1:100)、Bcl-2(1:100)、Bax(1:100)滴加于标本上进行孵育,湿盒内4℃过夜;
短句来源
     The results indicated that the titre of polyclonal antibody for rabbit to human IL-2R was 1: 10~4 by using ELISA, and the titre of the second antibody for goat to rabbit was 1 : 256 by means of immune diffu-sion test.
     结果,酶联免疫吸附试验(ELISA)测得兔抗人IL-2R多克隆抗体效价达1:10~4,免疫双向扩散法测得羊抗兔抗体效价高达1:256。
短句来源
     Monoclonal antibody (McAb) and polyclonal antibody to interleukin-2 receptor (IL-2R) and the second antibody labeled with horse radish peroxidase (HRP) were used to develop a high specific and sen-sitive sandwich type of enzyme-linked immunosorbent assay (ELISA) method to determine soluble IL-2R (sIL-2R).
     采用抗白细胞介素2受体(IL-2R)的单克隆与多克隆抗体以及辣根过氧化物酶(HRP)标记的羊抗兔IgG,建立了高特异性及高灵敏度的双抗体夹心法测定可溶性白细胞介素2受体(sIL-2R)。
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  anti-rabbit
The plant material was analyzed by ELISA using labeled anti-rabbit antibodies.
      
The material was analyzed by the method of competitive solid-phase immunoenzyme assay (ELISA) using peroxidase-labeled anti-rabbit antibodies.
      
Immobilization of peroxidase-labeled anti-rabbit IgG goat IgG, anti-peroxidase, peroxidase, and anti-alpha-fetoprotein was carried out with hydrophilic and hydrophobic monomers.
      
Individuals were then assayed for the presence of rabbit IgG by sandwich enzyme-linked immunosorbent assay (ELISA) using anti-rabbit IgG.
      
It showed that the goat anti-rabbit IgG had been labeled by fluorescence isothiocyanate (FITC).
      
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  anti rabbit
The organism was visualised using Rabbit serogroup 1 antibody and Sheep anti rabbit fluorescein conjugate.
      
Anti rabbit IgG was covalently coupled to this magnetizable cellulose.
      
After washing with PBS, bioti238 nylated swine anti rabbit serum was added, and 239 the cells were incubated for another 30 min.
      
After washing and fixation, the platelets were incubated with FITC-conjugated goat anti rabbit IgG and bound fluorescence analyzed by flow cytometry.
      
A polyvinylchloride plate was coated with donkey anti rabbit antibodies at 10 pg/ml and the remaining sites for protein binding were blocked by BSA.
      
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By using rabbit antibody against purified rat liver type L or type K pyruvate kinase (PyK) as the first antibody, and fluoresoein isothiocyanate-labelled sheep IgG against rabbit antibody as the second antibody, the localization of the type L and the type K PyK in normal rat liver, kidney and mouse Hep A ascites hepatoma (Hep A) has been studied by double antibody immunofluorescence method. It has been revealed that: (1) Type L PyK is located in parenohymal cells predominently, and type K PyK is mainly in Kupffer's...

By using rabbit antibody against purified rat liver type L or type K pyruvate kinase (PyK) as the first antibody, and fluoresoein isothiocyanate-labelled sheep IgG against rabbit antibody as the second antibody, the localization of the type L and the type K PyK in normal rat liver, kidney and mouse Hep A ascites hepatoma (Hep A) has been studied by double antibody immunofluorescence method. It has been revealed that: (1) Type L PyK is located in parenohymal cells predominently, and type K PyK is mainly in Kupffer's cells. (2) Hep A cells give strong fluorescence when stained by anti-type K PyK antibody. (3) In rat kidney, type L PyK is present in the cortex only, whereas type K PyK is located in both the cortex and the medulla in significant amount. The localization of the two types of PyK are in correlation with the difference of carbohydrate metabolism in the kidney cortex and medulla. The medulla contains more type K PyK than the cortex, so the oxidation rate in the medulla homogenate is lower than that in the cortex, whereas the glycolytio rate and the Orabtree effect are higher.

分别用兔抗大鼠L型或K型丙酮酸激酶(PyK)的抗体为第一抗体,并以异硫氰酸荧光素(FITC)标记的羊抗兔IgG为第二抗体,用双抗体法对正常大鼠肝、肾切片及小鼠HepA腹水肝癌(简称HepA)细胞涂片作免疫荧光染色,借以探讨L型及K型PyK在这些组织中的定位。结果发现:(1)L型PyK主要存在于肝实质细胞,而K型PyK可能主要存在于柯否细胞。(2)HepA细胞的胞浆,被K型PyK抗体染色后呈强烈的荧光。(3)L型PyK仅存在于大鼠肾脏皮质中,而K型PyK在大鼠肾皮质和髓质中均较丰富。以上两型PyK在肾脏中的分布与皮质和髓质的糖代谢特性不同是相一致的。因肾髓质较皮质含有较多的K型PyK,故其氧化率低于皮质,而酵解率和Crabtree效应高于皮质。

An investigation was made on the aortic wall of atherosclerotic rabbits by

用辣根过氧化物酶标记羊抗兔 IgG 对实验性动脉粥样硬化动脉壁行免疫酶标观察,发现主动脉内膜下及粥样斑块内有大量桔红色颗粒沉着。其结果表明酶标记羊抗兔 IgG是与动脉壁内的免疫球蛋白结合。动脉壁内大量 IgG 沉着提示有免疫复合物的沉积。免疫球蛋白与免疲复合物的形成对动脉粥样硬化的发生有密切的关系。

Immunomicrospheres prepared by covalent binding of sheep anti-rabbit IgG to car-boxylated polystyrene latex was used as solid phase second antibody in radioimmunoassay (RIA). It was compared with another solid phase second antibody "Immunosorbent" in the determination of LH, FSH and PEL. "Immunosorbent" and classical liquid phase double antibody RIA Kits for LH, FSH and PRL were supplied by WHO.It was found that in all these determinations the results obtained by solid phase methods and liquid phase method were...

Immunomicrospheres prepared by covalent binding of sheep anti-rabbit IgG to car-boxylated polystyrene latex was used as solid phase second antibody in radioimmunoassay (RIA). It was compared with another solid phase second antibody "Immunosorbent" in the determination of LH, FSH and PEL. "Immunosorbent" and classical liquid phase double antibody RIA Kits for LH, FSH and PRL were supplied by WHO.It was found that in all these determinations the results obtained by solid phase methods and liquid phase method were closely correlated, the coefficients of correlation were 0.97-0.99. The assays were more simple and precise by using solid phase second antibody, and Immunomicrospere was even better than "Immunosorbent" in some respects.

共价交联羊抗兔IgG到羧化聚苯乙烯胶乳上而制得的免疫微球,在放射免疫测定中被用作固相第二抗体。在 LH、FSH和PRL的测定中将免疫微球和另一个固相第二抗体“Immunosorbent”作了比较。“Immunosorbent”和LH、FSH、PRL放免液相双抗体法测定药盒均由世界卫生组织供应。在所有这些测定中,用固相法和液相法所获得的结果呈密切相关,相关系数在0.97~0.99之间。使用固相第二抗体可使测定更为精确、简便,而免疫微球在某些方面的效果比“Immunosorbent”更好些。

 
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