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抗鼠
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  anti-mouse
     The optimum concentrations were 1 μg/ml IgM and IgG for coating and 1: 2000 dilution of HRP-goat anti-mouse IgG for working.
     IgM和IgG最适包被浓度为1μg/ml,HRP-羊抗鼠IgG最适工作浓度为1:2000。
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     But as mouse McAb, HAMA(human anti-mouse antibody reaction) can be induced.
     但鼠源性McAb注入人体会引起人抗鼠抗体(HAMA)反应,因而应用受到限制。
短句来源
     AFB_1-BSA and donkey anti-mouse immunoglobulins were jet-positioned onto a nitrocellulose membrane which the distance was 4 mm.
     将AFB_1-BSA(检测线)和驴抗鼠IgG(质控线)分别喷在硝酸纤维素膜(Nitrocellulose membrane,NCM)上,检测线和质控线两者之间相距4mm。
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     2. After the interaction of HL - 60 and HBMEC , Observing changes of cells skeleton ( Rhodamine - conjugated phalloidin) and TJ ( anti - ZO - 1 antibody of mouse, FITC - conjugated anti -mouse IgG)by fluorescence.
     2.免疫荧光技术检测HL-60细胞与HBMEC相互作用后,HBMEC细胞骨架(罗丹明标记的毒伞素)和紧密连接(鼠抗ZO-1抗体,FITC标记的羊抗鼠抗体)的变化。
短句来源
     Traditional murine antibodies were limited by human anti-mouse antibody (HAMA) response, and humanized antibodies pave the way to solve this problem.
     由于人体对鼠源单克隆抗体能产生人抗鼠抗体反应(HAMA),人源单克隆抗体成为单克隆抗体应用于临床治疗的一个关键因素。
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  “抗鼠”译为未确定词的双语例句
     Results The configuration of IgG-gold molecule is an "ellipsoidal sphere" sized as(22.0 nm)×(9.0 nm)×(5.7 nm).
     结果羊抗鼠IgG胶体金分子为22.0 nm×9.0 nm×5.7 nm的“椭圆球状”结构。
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     mouse ascitic fluid antibldy (MAV-Ab),biotin-labeled sheep antibody of mouse (b-SAMG) and avidin-biotin-peroxidase complex (ABC) used for ABC-ELISA method were 5μg/ml, 1: 500 dilution, 1 : 2000 dilution and 1 : 300 dilution.
     此法所用试剂的工作浓度为,CMV的兔抗血清(RAV-IgG)5μg/ml,鼠腹水抗体(MAV-Ab)1:500,生物素化羊抗鼠IgG(b-SAMG)1:2000,亲和素与生物素化过氧化物酶复合试剂(ABC)1:300。
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     Genetic engineered IFN-α2b liposome to resist influenza virus(A/FM/1/47) was studied.
     研究基因工程α2b干扰素脂质体抗鼠肺敏感株流感病毒A/FM/1/47的作用。
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     Methods Forty C57BL/6 mice bearing LLC were divided into 4 groups and injected with 0.9% NaCl solution, OK-432, IL-2 and OK-432/IL-2. The inhibition of tumor growth after the drug administration and the expression of bcl-2 in paraffin-embedded primary tumor tissues were observed with SABC.
     方法 将40只C57BL/6荷瘤LLC小鼠分4组,分别用生理盐水、OK-432、IL-2和OK-432联合IL-2处理,观察用药后肿瘤生长的状况, 用抗鼠bcl-2单克隆抗体进行SABC免疫组化技术半定量测定Bcl-2在Lewis肺癌原发灶中的表达。
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     5% PVP could also enhance the effect of murine IgG1 to adhere to the T24 cells.
     PVP能提高抗鼠IgG1对T24细胞的黏附作用。
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  相似匹配句对
     Intervention with anti-H.
     H.
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     Anti-H.
     H .
短句来源
     Preparation of anti-T lymphocyte serum of mouse
     T淋巴细胞血清的制备(英文)
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     Effect of gentiopicroside on liver injury of rats
     龙胆苦甙肝损伤的作用
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  anti-mouse
An anti-mouse spermatozoon monoclonal antibody, MSH27, as well as its purified antigen, can block sperm-egg membrane fusion.
      
The conductance of monoclonal mouse IgG immobilized on polylysine-coated glass substrate changed from 1.02×10-8 Ω-1 to 1.41×10-11 Ω-1 at 10 V when complex is formed due to the specific biomolecular interactions with rabbit anti-mouse IgG F(ab')2.
      
Fluorescein-labeled goat anti-mouse antibody was used as second antibody.
      
The immunoglobulin G (IgG) fraction of goat anti-mouse IgG is used to coat wells of microtiter plates.
      
Protein-A or goat anti-mouse-Ig (GAMIg) covalently bound to agarose-polyacrolein microsphere beads (APAMB) were employed for the removal of T cells from human peripheral blood leukocytes (PBL) and bone marrow (BM).
      
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A new method was described for the determination of mouse T lymphocytes by using protein A-containing staphylococci labeled with rabbit anti-mouse brain antiserumi. The influencing factors and the specificity of the method were investigated. At the same time complement-dependent cytotoxicity test was used to measure T lymphocytes in spleen and lymph nodes of various mouse strains in parallel for the purpose of comparison.

本文报告用兔抗鼠脑血清标记含SPA菌体检测T淋巴细胞的方法,并探讨了有关影响因素以及本方法的特异性,同时用补体依赖性细胞毒试验,平行检测不同品系小鼠脾脏和淋巴结中的T淋巴细胞数,以资对比。

Detection of specific IgC Trichosanthes kirilowii Maixm(TKM) in mice with ELISA is described. The poor adhering ability of TKM onto polyty-rene surface and appearance of nonspecific reaction were solved by coating TKM to the plate indirectly with chicken anti-TKM serum(γ-globulin fraction), first adsorbed to the plate. This improvement made it possible to detect specific IgG quantitatively. The optimal conditions for the test were: γ-fraction of chicken anti-TKM serum 50μg/ml, TKM 50μ/ml and the conjugate 1...

Detection of specific IgC Trichosanthes kirilowii Maixm(TKM) in mice with ELISA is described. The poor adhering ability of TKM onto polyty-rene surface and appearance of nonspecific reaction were solved by coating TKM to the plate indirectly with chicken anti-TKM serum(γ-globulin fraction), first adsorbed to the plate. This improvement made it possible to detect specific IgG quantitatively. The optimal conditions for the test were: γ-fraction of chicken anti-TKM serum 50μg/ml, TKM 50μ/ml and the conjugate 1 : 1000. The specificity of this method was confirmed with inhibition test and its coefficient variance was 4.0-10.4%. 501 samples tested all gave satisfactory results. Methods used for coating poor adhering antigens and eliminating nonspecific adsorption of antibodies to the polystyrene surface were discussed.

用鸡抗天花粉免疫血清的γ球蛋白部分预先包被聚苯乙烯微量凹孔板,4℃过夜,依次加天花粉待测小鼠血清及兔抗鼠IgG-辣根过氧化物酶结合物,克服了因天花粉直接包被不完全而引起的非特异性免疫反应,获得了满意结果。测定了本法的特异性、重复性及标准曲线。讨论了清除非特异反应的方法。

Several techniques were used to identify the surface markers in mouse L615 cells. These cells did not show B cell surface markers, such as surface immunoglobulin after indirect immunofluorescence staining, nor Fc-recptor and complement-receptors by ro- sette formation. However, they were found to react specifically with rabbit anti- mouse brain serum and rabbit anti-mouse thymocytes serum by indirect immunofluores- cence staining and cytotoaicity assay, indicating the cells possessed Thy-1 antigen and the mouse-specific...

Several techniques were used to identify the surface markers in mouse L615 cells. These cells did not show B cell surface markers, such as surface immunoglobulin after indirect immunofluorescence staining, nor Fc-recptor and complement-receptors by ro- sette formation. However, they were found to react specifically with rabbit anti- mouse brain serum and rabbit anti-mouse thymocytes serum by indirect immunofluores- cence staining and cytotoaicity assay, indicating the cells possessed Thy-1 antigen and the mouse-specific lymphocyte antigen(MSLA)that were specific of T-cells. It is con- cluded that mouse leukemia L615 was a T-cell type leukemia.

为确定L615小鼠白血病的细胞类型,作者采用了多种淋巴细胞表面标志的检测技术,研究了L615白血病细胞的表面标志。结果表明,L615白血病细胞不具有B细胞的各种表面标志;诸如SmIg、IgG-FcR以及CR等。但它却与兔抗鼠脑血清和兔抗鼠胸腺细胞血清起特异性反应,表明它具有T细胞所特有的表面抗原-Thy-1和MsLA。由此确定,L615小鼠白血病是一株T细胞型白血病病株。

 
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