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亲和力     
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  affinity
     Design and selection of high affinity DNA ligands for mutant single-chain derivatives of the bacteriophage 434 repressor
     噬菌体434单链阻遏蛋白的高亲和力DNA结合序列的设计和`筛选
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     Research of Anti-hTNF-α Chimeric Antibody Affinity Maturation in Vitro
     人TNF-α嵌合抗体体外亲和力成熟作用研究
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     In Vitro Affinity Maturation of an Anti-TNFα Antibody
     抗TNFα抗体的体外亲和力成熟
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     Association of HLA-DRB1、IL-4、IL-13、PAF-AH and High Affinity Receptor for Immunoglobulin E Gene Polymorphisms with Asthma in Children
     儿童哮喘与HLA-DRB1、IL-4、IL-13、PAF-AH及IgE高亲和力受体-β链基因多态性的关联研究
短句来源
     Affinity Maturation and Characterization of Human Anit-Met Recombinant Antibody
     抗Met基因工程抗体的亲和力成熟与特性研究
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  appetency
     the adsorption appetency order of peat on heavy metals: Zn2+>Mn2+>Cu2+>Cd2+>Pb2+;
     草炭对重金属的吸附亲和力顺序为:Zn~(2+)>Mn~(2+)>Cu~(2+)>Cd~(2+)>Pb~(2+);
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     It is the basic reason of increase oxidation that the appetency of Sn-0.7Cu with oxygen is larger than Sn-37Pb and the surface film is loose.
     指出Sn-0.7Cu合金与氧的亲和力大于Sn-37Pb,且表面氧化膜疏松,是造成氧化速度快的根本原因;
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     Under the condition of potassium deficiency, the variety with stronger tolerance to low potassium stress had a higher appetency to potassium.
     在低钾胁迫下,早稻耐低钾品种对钾离子的亲和力明显高于不耐低钾品种,晚稻两品种间对钾离子的亲和力无明显差异.
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     The Michaelis constant of the immobilized glucoamylase was 22.63 mg/L. C ompared to the free enzyme(34.62 mg/L),the appetency of the immobilized enzymes to the substrate increased.
     米氏常数22.63mg/L,与游离酶(34.62mg/L)相比,对底物的亲和力增强;
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     The fit coefficient shows,the adsorption stabilization,the adsorption ability and appetency of Zn~(2+) are better than those of Cd~(2+).
     拟合系数显示,EPS对Zn2+的吸附稳定性、吸附能力和亲和力均比对Cd2+的吸附强.
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  affinity of
     The cellular affinity of BGC-823 was as follows:Kd= (37.82± 1.42) nmol/L, capacity of Bmax = (475.00± 17.86) pmol/mg.
     BGC-823细胞亲和力:Kd=(37.82±1.42) nmol/L,容量Bmax=475.00±17.86 pmol/mg。
短句来源
     The affinity of the antibody determined by iELISA was 1.8×10~8 L/moL.
     经间接ELISA方法测定,抗体的亲和力为1.8×108L/moL。
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     CDR3 mutagenesis improves the affinity of anti-TNF-α antibody Fab
     CDR3突变提高抗TNF-αFab段的亲和力
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     Results:Compared with progesterone, the relative binding affinity of mi-fepristone is396.67±25.32, and the 50% inhibitory concentration is (6.61±1.20) nmol/L;
     结果:与孕酮相比较,米非司酮的相对结合亲和力(RBA)为396.67±25.32,50%抑制浓度(IC50)为(6.61±1.20)nmol/L,P<0.01;
短句来源
     The affinity of d-berbamine, tetrahydrocoptisine and B_1, a synthetic protoberberine derivative, was relatively high with K_i values of 1.9×10~(-7), 6.8×10~(-7) and 8.1×10~(-7) mol/L respectively.
     小檗胺、四氢黄连碱和半合成原小檗碱衍生物B_1亦具有较高亲和力,K_i值分别为1.9×10~(-7),6.8×10~(-7)和8.1×10~(-7)mol/L。
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  binding affinity
     Results:Compared with progesterone, the relative binding affinity of mi-fepristone is396.67±25.32, and the 50% inhibitory concentration is (6.61±1.20) nmol/L;
     结果:与孕酮相比较,米非司酮的相对结合亲和力(RBA)为396.67±25.32,50%抑制浓度(IC50)为(6.61±1.20)nmol/L,P<0.01;
短句来源
     IC 50,DCXW =3.6×10 -2 mg/ml. Relative binding affinity of DCXW=18.1%.
     DCXW的 IC5 0 值为 3.6× 10 - 2 m g/ ml,相对结合亲和力为18.1% (相对于 L osartan)。
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     Conclusion The prediction of HLA-A*0201 restricted epitopes from CT antigen KM-HN-1 and the peptide HLA-A*0201 binding affinity & complex stability assay of the 5 candidate peptides provide experimental data for identification of HLA-A*0201 restricted epitopes from KM-HN-1.
     结论基于蛋白酶体剪切位点特异性的算法及基于肽MHC-Ⅰ结合的算法对KM-HN-1进行HLA-A*0201限制性表位预测,结合候选表位肽与HLA-A*0201分子结合的亲和力与复合物稳定性实验分析,为该抗原HLA-A*0201限制性表位的鉴定奠定了基础。
短句来源
     Results The percent inhibitory values (IC 50 ) of E 2 was 1×10 -9 mol/L. BPA and p-NP can inhibit of 3H-E 2 binding to rat uterine cycotol estrogen receptor with an IC 50 of 2.08×10 -5 mol/L and 2.66×10 -5 mol/L,respectively. The relative binding affinity(RBA) of BPA and p-NP were 0.004?
     结果 E2 的IC50 是 1× 10 -9mol/L ,BPA、p -NP的IC50 分别为 2 0 8× 10 -5mol/L和2 6 6R10 -5mol/L ,BPA、p -NP的相对结合亲和力系数 (RBA)分别为 0 0 0 4 8和 0 0 0 38,BPA与ER的结合能力稍高于 p -NP。
短句来源
     the interaction of galactose molecules with Ca2+-β-sialic acid binary complex enhances the binding affinity of sialic acid molecule for Ca2+ in binary complex, and the binding constant is about 121.5M-1.
     半乳糖对Ca~(2+)-唾液酸的二元复合物的作用,增强了二元复合物中唾液酸与Ca~(2+)的亲和力,其结合常数为121.5M~(-1).
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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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  appetency
hepatica infections, and/or by the fact that Tetraphyll would not have the same appetency for all populations of G.
      
The appetency of the first one for the second is defined from the properties of the support and the new layer-essentially in its liquid phase-as well as from the environmental conditions.
      
Formation of the whole interfacial layer provides the appetency for the growth of (111) Hg1-xCdxTe epilayer on (211) Si substrate.
      
  affinity of
Both these models predicted binding affinity of internal and external test set compounds including the enantiomers of compound no.
      
Using the osteoblast culture technique, we detected cell behaviors on the biomaterial in vitro by SEM, and the cell affinity of the composite was found to be higher than that of the PLA scaffold.
      
The affinity of the recombinant human RI with double site mutation was examined for RNase A and its anti-oxidative effect.
      
Fast deposition of hydroxyapatite coating on titanium to modify cell affinity of corneal fibroblast in vitro
      
In the case of AcLDC, this dependence was hyperbolic and the affinity of the enzyme for its substrate was high (Km = 20 mM).
      
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  binding 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.
      
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.
      
DNA binding affinity (ΔTm) of the tested compounds did not correlate with either their anti-P.
      
All of these show that huperzine E has high binding affinity with AchE.
      
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