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   affinity 在 生物医学工程 分类中 的翻译结果: 查询用时:0.102秒
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  亲和
    A Novel SDE-grafted Affinity Adsorbent Mimicked the Ligand Function of LDL Receptor
    一种接有仿LDL受体功能结构短肽SDE的LDL亲和吸附剂的研究
短句来源
    Bilirubin removal by chelating metal Copper ion CA/PEI affinity membrane
    CA/PEI螯合铜亲和膜吸附胆红素的初探
    The titers of antiserum were 1:1000-1:3500 and affinity constant was 3.45×10 ̄9l/mol. The cross reactions with β_2-MG,Alband IgG were less than 0.003%.
    抗血清稀释度为1:1000-1:3500,亲和常数为3.45×10 ̄9l/ml,与β_2-MG,白蛋白、IgG的交叉反应小于0.003%。
短句来源
    The affinity constant of rhirudin with thrombin-fibrin complex was 9.72×10~6L/mol, and the physiological Ca~(2+) concentration was their optimal binding environment.
    生理Ca~(2+)浓度是它们的最佳结合环境,水蛭素与凝血酶-纤维蛋白原复合物结合的亲和常数K_a为9.72 ×10~6L/mol;
短句来源
    Culture medium of 4B3 cells was purified with streamline SP ion exchange chromatography and Lysine Sepharose 4B affinity chromatography, the purity of rt PA reached 98%.
    细胞培养上清经StreamlineSP离子交换层析和Lysine Sepharose 4B亲和层析两步纯化 ,获得纯度达到 98%的rt PA。
短句来源
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  亲和力
    Results: “In vitro” and “in vivo” opioid receptor binding studies showed very high affinity (Ki=4×10-4 μmol/L), 63% of 20minpostinjection specific binding and good imaging as a degradationresistant of this agent in mouse brain.
    结果:体外和体内阿片受体结合分析表明这一新的阿片配体具有非常高的亲和力(Ki=4×10-4μmol/L)。 注药后20min动物脑内的特异性结合占63%,且其在脑内滞留时间较长而有利于成像。
短句来源
    99Tcm-RC-160 have high affinity with somatostatin receptor (Kd = 0. 83 + 0. 09 nmol/L,Bmax = 45 + 3 nmol/g).
    标记物与受体有较高的亲和力(K_d=0.83±0.09 nmol/L,B_(max)=45±3nmol/g)。
短句来源
    The affinity of P19 to hydroxyapatite(HA) and the osteogenous activity of UMR106 were observed.
    观察P19对HA的亲和力和表面培养UMR106细胞的成骨活性。
短句来源
    Results :1. Better hydrophilia and cell affinity of collagen-chitosan complex scaffold, subcutaneous experiment showed good biological compatibility, in vivo.
    结果:1.胶原-壳聚糖复合材料具有良好的亲水性和细胞亲和力,皮内埋置实验显示生物相容性好,体内降解时间为8~10周; 2.骨髓细胞基质干细胞(BMSCs)贴壁生长,在生长因子等诱导下可分化为内皮细胞,细胞生长曲线良好。
短句来源
    and the study also should be made in deep on themechanism and the differences of the affinity of various organs and tissues to nickel and titanium.
    不同器官及组织对镍、钛的亲和力差异及其机制尚待深入探讨。
短句来源
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  亲和性
    Objective: To evaluate the cellular affinity of RGD peptide modified PLGA/HA(poly lactic coglycolic acid/ hydroxyapatite) film.
    目的:研究将RGD肽结合至聚乳酸基复合材料-聚乙交脂丙交脂与羟基磷灰石的复合物,形成的新型RGD-PLGA/HA(RGD peptide modified poly lactic-glycolic acid/hydroxyapatite)膜材料的细胞亲和性
短句来源
    RESEARCH ON CELL AFFINITY OF POLY-L-LACTIDE/PORCINE-DERIVED XENOGENEIC BONE COMPOSITE IN VITRO
    聚丙交酯-猪衍生异种骨复合材料的体外细胞亲和性研究
短句来源
    Study on the Cellular Affinity of RGD Modified PLGA/HA Film
    RGD-PLGA/HA膜材料的细胞亲和性实验研究
短句来源
    Study on Modification of Poly(Lactide) Film by Low-temperature Plasma and Its Cell Affinity
    聚乳酸膜低温等离子改性及其细胞亲和性研究
短句来源
    In this research, the NH_3/O_2 plasma and plasma grafting after Ar plasma treatment were used to modify its surface in order to improve its hydrophilicity, and discussed the affection on the amino density of material surface, the grafting density of PVP, the surface form before and after treatment, the change of contact-angle by different treatment conditions and make research on the cell affinity of modified materials.
    本文采用NH_3、O_2等离子法直接作用和Ar等离子处理接枝聚乙烯吡咯烷酮(PVP)的方法对其进行处理,以改善其表面亲水性,探讨了不同处理条件对材料表面氨基密度,PVP的接枝密度,处理前后材料的表面形态,表面接触角的变化的影响,并对改性后的材料的细胞亲和性进行了研究。
短句来源
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  亲合力
    FIBRINOGEN ADSORBED TO DIFFERENT POLYMER BIOMATERIALS AND STUDYING ON MONOCLONAL ANTIBODY M1 BINDING AFFINITY
    几种不同高分子生物材料吸附FG与单克隆抗体M1结合亲合力的研究
短句来源
    The binding of this compound with PNA receptor has high affinity and specificity. 
    它与PNA受体结合,具有亲合力高及特异性强的生物活性。
短句来源
    Using monoclonal antibody M1 as a substitute of the platelet the binding affinity of FG M1 complex of a few polymer biomaterials was measured by ELISA. Compared the changs in binding affinity of M1 to one of the platelet binding domain of FG adsorbed to different materials so that evaluated the blood compatibility of those polymer biomaterials.
    利用鼠抗人血纤维蛋白原(Fibrinogen,FG)单克隆抗体M1作为血小板替代物,以酶联免疫吸附测定(EnzymeLinkedlmmusorbentAssay,ELISA)为手段,通过FG-M1复合物结合亲合力常数ka的测定,对几种高聚物材料血液相容性进行了评价.测定了不同材料表面的XPS谱,比较了不同组成的材料表面血液相容性的差异
短句来源
    Using this model, the predictive sets are predicted for binding affinity of peptide-MHC complex molecule, and the result is satisfying.
    用该模型对预测样本进行短肽-MHC 分子的结合亲合力的预测,结果令人满意。
    In this paper, a binding affinity model of peptide-MHC complex molecule is studied by QSAR method based on partial least squares (PLS), and it results a satisfied formula between the binding affinity of peptide-MHC complex molecule and the sequence of peptide.
    本文基于偏最小二乘法(PLS)研究了CTL表位与MHC分子结合的定量构效关系模型, 得到比较满意的短肽-MHC分子结合亲合力与短肽序列之间的关系式。

 

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  affinity
3D-QSAR STUDIES ON SUBSTITUTED DIHYDROPYRIDINES FOR THEIR α1A-ADRENERGIC RECEPTOR BINDING AFFINITY
      
Both these models predicted binding affinity of internal and external test set compounds including the enantiomers of compound no.
      
For example, N1-(4-aminobenzenesulfonyl)-5-azaskatole (18; Ki = 41 nM) displayed an affinity comparable to N1-(4-aminobenzenesulfonyl)skatole.
      
All compounds were characterized by binding affinity determination for 5-HT2A and 5-HT2C subtypes and antagonistic activity for 5-HT2B receptor in rat stomach fundus.
      
None of the new compounds showed affinity for 5-HT2A and 5-HT2C subtypes, but some of them displayed antagonistic activity in rat stomach fundus at micromolar concentrations.
      
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