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   cell binding 的翻译结果: 查询用时:0.178秒
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cell binding
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  细胞结合
     Results The cell binding rates of 99mTc-CL3-Bt and 99mTc-CL3 were 90% and 94%, and their ID%/g of tumor averaged 6.3±1.1 and 6.7±0.9 respectively, which were statistically comparable (t=0.6293,P>0.05);
     结果99mTc-CL3-Bt和99mTc-CL3的细胞结合率分别为90%、94%; 在瘤体的ID%/g值分别为(6.3±1.1)、(6.7±0.9),二者无显著差异(t=0.6293, P>0.05);
短句来源
     Methods Monoclonal antibody (Mab) CL3 binding to biotin was reduced with 2-mercaptoethanol (2-ME) and labeled directly with 99mTc to produce 99mTc-CL3. The immunoactivity of 99mTc-CL3-Bt and 99mTc-CL3 was measured by cell binding test and the results compared;
     方法 将单抗CL3生物素(Bt)化,以2-巯基乙醇(2-ME)还原后以直接法进行99mTc 标记。 以细胞结合实验测定并比较99mTc-CL3-Bt 和99mTc-CL3的免疫活性;
短句来源
     Inhibition of collagen-induced arthritis by HLA-DRβ1 specific non-T cell binding peptide
     HLA-DRβ1特异性非T细胞结合肽对胶原性关节炎的抑制作用
短句来源
     Immunoreactivity of 125I- anti-Tg- McAb(18A1 and 18A11) with cells of normal thyroid and tumor was determined by cell binding assay.
     选用自制的18A_1和18A_(11)两株McAb进行体外活细胞结合实验,定量观察~(125)I标记的18A_1和18A_(11)与正常甲状腺组织细胞及某些肿瘤细胞膜结合的反应性。
短句来源
     Methods (1)sc-7269 was labeled with Na~(131)I using the Iodogen method,subsequently separated the ~(131)I-sc-7269 by sephadex G-50 column chromatography. Then immune activity of ~(131)I-sc-7269 was identified using T24 cell binding analysis in vitro.
     方法(1)Iodogen法标记抗-VEGFMcAb(sc-7269),SephadexG-50柱层析分离纯化制备131I-sc-7269,体外细胞结合分析检测标记抗体的免疫活性;
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  “cell binding”译为未确定词的双语例句
     The effects of regenerating liver cytosol(RLC)on serum insulin and C-peptide levels,and liver cell binding specific(~(125)I)iodoinsulin were studied in rats with liver injury induced by D-galactosamine(Galn).
     研究了再生肝胞液(RLC)对实验性肝损伤大鼠血清胰岛素、C-肽水平及肝细胞结合A14[~(125)I]、胰岛素的影响;
短句来源
     Pseudomonas exotoxin A is a single-chain cytotoxin composed of three structural domains. Domain I a (1-255 aa) is responsible for cell binding, domain II (253-364 aa) for membrane translocation enabling access to the cytosol, domain 111(400-613 aa) for the catalytic inactivation of protein synthesis, domain I b (265-399 aa) which has no clear function.
     PE(Pseudomonas exotoxin A)是绿脓杆菌分泌的单链毒素,由613个氨基酸组成,分为三个主要的结构域:结构域Ia(1-252 aa)的作用是识别并结合靶细胞:结构域Ⅱ(253-364 aa)具有内吞体转位活性; 结构域Ⅲ(400-613aa)催化延长因子EF-2 ADP-核糖基化而使其失活。
短句来源
     The expression of ICAM-1, CD44 and HLA-I was determined by fluorescence-activated cell sorter (FACS) analysis, the tumor cell binding affinity to extracellular matrix (ECM) components was measured by cell attachment assay, the degree of homotypic aggregation was quantified by cell aggregation assay.
     结果 :经高浓度和低浓度IL 4处理后 ,肝癌细胞表面ICAM 1及HLA I类抗原表达均增加 ,CD44表达减少 ,肝癌细胞对细胞外基质的亲和力及肝癌细胞聚集程度均降低。
短句来源
     Multiple regression analysis demonstrated a positive relationship between mononuclear cell binding and fasting plasma glucose( r =0 041, P <0 01).
     (2)经多元回归分析,空腹血糖与单核细胞内皮细胞黏附率呈正相关(r=0041,P<001)。
短句来源
     Non-T cell binding peptide yielded hyporesponse to CⅡ specific T cell activation,suggesting a new strategy of immunosuppresive therapy in RA.
     低T细胞反应性CⅡ修饰肽可能对类风湿关节炎的T细胞激活有抑制作用
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  相似匹配句对
     Con A binding to the AS cell was improved.
     AS细胞的蛋白质发生了N-糖基化修饰。
短句来源
     (4) Con A binding to the AS cell was increased.
     (4)ConA与AS细胞的结合增强。
短句来源
     g per cell;
     g时,仅有少数细胞蓝染呈阳性;
短句来源
     Introduction on Z-Cell
     Z-元件介绍
短句来源
     protein binding;
     蛋白结合;
短句来源
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  cell binding
Plaque accumulation may be mediated by bacterial extracellular polysaccharides, salivary components as well as direct cell-to-cell binding.
      
In this study we present methods to physico-chemically modify micropatterned cell culture substrates that were manufactured using plasma lithography to incorporate affinity structures for specific cell binding.
      
A theoretical model is developed for cell-to-cell binding by bivalent ligands that can bind to mobile receptors on the cell surfaces.
      
This activity could be harnessed by coupling RNases to cell binding ligands for the purpose of engineering them into cell-type specific cytotoxins.
      
Evidence that α5β1 integrins mediate Leydig cell binding to fibronectin and enhance Leydig cell proliferation stimulated by a Se
      
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This paper dealt with the application of polyurethane as a carrier to immobilize E. coli penicillin acylase to hydrolyze penicillin G into 6-aminopenicillanic acid.A series of tests has been made to get the best ratio between the quantity of E. coli cells and materials of preparation of E.colt cells bound to polyurethane, by the orthogonal test method. The thermal and pH stabilities of the enzyme are greatly increased in immobilized form than in intact E. coli cells, and therefore, it can be...

This paper dealt with the application of polyurethane as a carrier to immobilize E. coli penicillin acylase to hydrolyze penicillin G into 6-aminopenicillanic acid.A series of tests has been made to get the best ratio between the quantity of E. coli cells and materials of preparation of E.colt cells bound to polyurethane, by the orthogonal test method. The thermal and pH stabilities of the enzyme are greatly increased in immobilized form than in intact E. coli cells, and therefore, it can be used repeatedly.

应用聚氨酯泡沫塑料做载体,固定大肠杆菌青霉素酰化酶,可用于青霉素G钾盐的水解制备6-氨基青霉烷酸。实验采用正交设计法,对制备聚氨酯泡沫固定化大肠杆菌的原料和菌体之间的配比,作了系统试验,获得较理想的配方。制成的固定化细胞与天然菌体相比,对热pH稳定性均有明显提高,可重复用于青霉素G钾盐的水解。

The cell-bound penicillinase and exopenicillinase were excreted by the S.aureus75 strain isolated clinically in Nanjing,but no cell-bound exopenicillinase was de-monstrated.When the exponentially growing cultures were induced by adding oxacillinalone,penicillinase produced was at a low rate in the cultures.However,if sodiumcitrate is placed in the culture medium before,the production of the penicillinase byoxacillin was increased in a large amount in the cultures.When the concentration...

The cell-bound penicillinase and exopenicillinase were excreted by the S.aureus75 strain isolated clinically in Nanjing,but no cell-bound exopenicillinase was de-monstrated.When the exponentially growing cultures were induced by adding oxacillinalone,penicillinase produced was at a low rate in the cultures.However,if sodiumcitrate is placed in the culture medium before,the production of the penicillinase byoxacillin was increased in a large amount in the cultures.When the concentration ofthe sodium citrate in the medium was 0.15Mthe specific activity of the total penicil-linase and the exopenicillinase in the cultures over a period of 18 hrs.was about8.7 and 16.9 fold respectively as much as that in control.The staphylococcal exopenicillinase was purified by the modified Richmond'smethod,the total recovery being 25.33% and the specific activity being 21729units/μ g of protein.

南京临床分离的耐药性金黄色葡萄球菌75号菌株产生细胞结合青霉素酶和胞外青霉素酶,但未能证明有细胞结合胞外青霉素酶。于对数生长期的培养物中加入苯唑青霉素,青霉素酶的产生率较低;如于培养基中加入柠檬酸钠,则笨唑青霉素对青霉素酶的诱导作用显著增加。以0.15M 柠檬酸钠对青霉素酶产生的刺激效果最显著。总酶和胞外酶的活力分别是未加柠檬酸钠培养基的8.7和16.9倍。柠檬酸钠的加入对细菌的生长有明显的抑制作用。用改良的 Richmond 方法纯化葡萄球菌胞外青霉素酶,平均总收率为25.33%,其平均比活力为21729单位/微克蛋白。

Using SPA coated OEBG as specific indicator cells bound to rabbit anti-human im-munoglobulin antibodies for the detection of B lymphocytes of human peripheral blood.DIF was used to determine B lymphocytes of the same samples in parallel for the purpose of comparison.Results expressed as mean percentage of lymphocytes reacting with specific indicator ORBC standard deviation. B lymphocytes of normal human peripheral blood was recorded as (14.7 ± 2%) and (12.2 ± 1.8%) respectively from twenty individuals...

Using SPA coated OEBG as specific indicator cells bound to rabbit anti-human im-munoglobulin antibodies for the detection of B lymphocytes of human peripheral blood.DIF was used to determine B lymphocytes of the same samples in parallel for the purpose of comparison.Results expressed as mean percentage of lymphocytes reacting with specific indicator ORBC standard deviation. B lymphocytes of normal human peripheral blood was recorded as (14.7 ± 2%) and (12.2 ± 1.8%) respectively from twenty individuals (P<0.001); B lymphocytes of nasopharyngeal carcinoma patient's peripheral blood was recorded as (29.5 ± 6.0%) and (25.5 ± 5.4%) respectively from twenty-four individuals (P<0.0005) ; lymphocyte suspension in B-enriched preparations by Nylon Wool column separation was recorded as (45.4 ± 4.2%) and (41.1 ± 4.0;%) respectively from eighteen individuals (P<0.001). The difference between the two methods was highly significant by the student's t-test.These findings suggested that SPA indirect resetting reactions was more sensitive and specific than DIF. And also because of its simplicity in application no fluorescent microscope is required, it was more advantageous and could be used in place of DIF in detecting B lymphocytes of human peripheral blood.

本文介绍一项检测B淋巴细胞的SPA间接花环试验,其原理是以包被有SPA的牛红细胞作为指示红细胞(ES),使ES同抗人Ig的IgG型抗体(A)结合形成ESA复合物,当SmIg+的B淋巴细胞与ESA反应后,就可以形成SPA间接玫瑰花环。文中对其影响因素作了探讨。此外,将本法与直接免疫荧光(DIF)法同时作平行试验,结果表明本法的敏感性和特异性超过了DIF(P<0.001)。本方法具有许多优点,可替代DIF以检测人外周血B淋巴细胞。

 
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