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reversible binding
相关语句
  可逆结合
     At room temperature, we study the action between two tailed imidazole porphyrincobalts (Ⅱ) and oxygen by UVVis spectrum. The result exhibits that the two tailed imidazole porphyrincobalts(Ⅱ) have not the ability of reversible binding of oxygen at room temperature.
     通过UVVIS光谱研究了两种咪唑基尾式卟啉钴在室温下与氧的作用,结果表明,在室温下这两种尾式卟啉均未呈现与氧可逆结合的特性.
短句来源
     Domain Ⅱ is involved in receptor binding,including the reversible binding and irreversible binding.
     结构域Ⅱ参与与受体的结合 ,包括可逆结合和不可逆结合 ;
短句来源
  “reversible binding”译为未确定词的双语例句
     The maximum specific binding capacity (B max) was (3 28±0 31) μg/g. The results showed that there were specific, saturable, and reversible binding site of apoCⅢ on HepG2 cells, and it was identified that HepG2 cell line was a useful model for the study of human hepatic apoCⅢ receptor.
     结果证实HepG2细胞上存在高亲和力的、可饱和的、特异的apoCⅢ受体结合位点 ,其受体的亲和力 (Kd)和apoCⅢ受体结合容量 (Bmax)分别为(9 5 3± 1 0 3)× 10 -9mol/L和 (3 2 8± 0 31) μg/ g .
短句来源
     The tests of saturable binding, reversible binding, competition binding and time-temperature binding between 125I-γ-Ty-Folate and β-lactoglobulin were carried out, and the receptor binding test was performed between 125I-γ-Ty-Folate and HeLa cells.
     12 5I Ty Folate与叶酸结合蛋白 β 乳球蛋白 (β lactoglobulin)进行饱和结合实验、蛋白解离实验、竞争结合实验和动力学实验 ,与HeLa细胞进行了饱和实验。
短句来源
     REVERSIBLE BINDING OF NALOXAZINE AND 14-HYDROXYDIHYDROMORPHAZINE WITH OPIATE RECEPTORS
     纳洛肼及14-羟基双氢吗啡肼与阿片受点结合的可逆性
短句来源
     Furthermore, a satisfactory saturable, specific, and reversible binding was demonstrated with Kd of (6.9±0.6) nmol·L-1, Bmax of (74±6) fmol/107 cells.
     Ohm 0.1-1μmol·L~(-1)能够抑制活化的淋巴细胞增殖。
短句来源
  相似匹配句对
     The binding was rapid saturable,temperature dependent and reversible.
     其特异结合是快速的、可饱和的、可逆的、依赖温度的;
短句来源
     REVERSIBLE BINDING OF NALOXAZINE AND 14-HYDROXYDIHYDROMORPHAZINE WITH OPIATE RECEPTORS
     纳洛肼及14-羟基双氢吗啡肼与阿片受点结合的可逆性
短句来源
     Reversible Renascence
     可逆转性的重生
短句来源
     protein binding;
     蛋白结合;
短句来源
     THE SUBSTRATE BINDING OF TRYPSIN
     胰蛋白酶与底物在尿素溶液中的结合
短句来源
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  reversible binding
These results suggest that a reversible binding between virion and albumin may occur in vivo and does not require chemical modification or cross-linking.
      
Several lines of evidence from reversible binding studies seem to indicate there are at least two "central" benzodiazepine receptor subtypes, the BZ1 and BZ2 receptors.
      
The reversible binding of O2 to the axial 5-position was shown for the freshly sublimed layers: the 6-position can either be free, or occupied by the pyridyl group of the adjacent molecule in the layer.
      
Structural features of sublimed layers of meso-mono-4-pyridyltriphenylporphyrinatocobalt(ii) and reversible binding of molecular
      
Recombinant human serum albumin (rHSA), secreted by a Pichia pastorisexpression system, was purified by a fast and efficient method, the essential feature of which is strong but reversible binding of the protein to Blue Sepharose.
      
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This paper reports the properties of photoaffinity labeling of benzodiaze pine receptors (BDZ-R) of bovine cerebral cortex. Photoaffinity labeling was specific and saturatble and could be inhibited by Spine benzodiazepines such as clonazepamand delorazepam. The inhibition constants of both clonazepam and delorazepam in inhibiting the photoaffinity labeling of [3H] flunitrazepam ([3H]FNZP) on BDZ-R were very close to those in inhibiting the reversible binding of [3H] FNZP and BDZ-R, suggesting that the...

This paper reports the properties of photoaffinity labeling of benzodiaze pine receptors (BDZ-R) of bovine cerebral cortex. Photoaffinity labeling was specific and saturatble and could be inhibited by Spine benzodiazepines such as clonazepamand delorazepam. The inhibition constants of both clonazepam and delorazepam in inhibiting the photoaffinity labeling of [3H] flunitrazepam ([3H]FNZP) on BDZ-R were very close to those in inhibiting the reversible binding of [3H] FNZP and BDZ-R, suggesting that the photoaffinity labeling of [3H]FNZP and BDZ-R might be taken place at the same sites as that of the reversible binding. The photoaffinity labeling depends on the illumination time. The optimum illumination time was 25 min in our experiment. The efficiency of photoaffinity labeling in this paper was 77%, much higher than the values (20-25%) found in the lite-ratures. The BDZ-R subunit molecular weight, determined by combining photoaffinity labeling with HPLC, was 48 000±1000.

本文报道牛大脑突触膜上苯二氮受体(BDZ-R)的光亲和标记性质。光亲和标记是特异性的,可饱和的,并可被苯二氮类药物抑制,其抑制常数K_1与可逆结合实验值相似,推测光亲和标记与可逆结合发生在BDZ-R的相同部位。已知光亲和标记与时间有关,本文采用254nm短波长紫外光源,25min为最佳光照时间,其光亲和标记效率最大为77%。光亲和标记与高压液相色谱技术联用,测得BDZ-R的亚基分子量为48000±1000。

The C1q receptor (C1qR) on the human T lymphocyte line Jurkat cells was demonstrated and characterized. Cell-ELISA showed that Jurkat cells are able to bind exogenous C1q and recognized by the anti-C1qRantibody 112. FCM analysis indicated that the binding of FITC-C1q to Jurkat cells is blocked by an excess of unlabelled C1q.Quantitative binding studies with monomeric 125 I-C1q showed a specific, dose-dependent,saturable and reversible binding involving specific membrane receptors on Jurkat cells, Goldstein...

The C1q receptor (C1qR) on the human T lymphocyte line Jurkat cells was demonstrated and characterized. Cell-ELISA showed that Jurkat cells are able to bind exogenous C1q and recognized by the anti-C1qRantibody 112. FCM analysis indicated that the binding of FITC-C1q to Jurkat cells is blocked by an excess of unlabelled C1q.Quantitative binding studies with monomeric 125 I-C1q showed a specific, dose-dependent,saturable and reversible binding involving specific membrane receptors on Jurkat cells, Goldstein analysis and Hill plot of C1q binding showed 1. 1 × 106 binding sites per cell with an average affinity of 1. 5 ×107 mol-1and a Hill number of 0.9643 at normal ionic strength (I = 0. 15 ) and temperature (37℃).The experiment with the anti-C1q monoclonal antibody A4, which recognizes the collagen-like region (CLR) of C1q, established that it is via its CLR that C1q binds to Jurkat cell receptors.Western blotting with the anti-C1qR antibody 112 revealed that the C1qR on Jurkat cells is a membrane protein of 70 ku.

采用酶联免疫吸附试验、流式细胞术、放射配体结合试验及蛋白质印迹等方法,首次证实了人T细胞系Jurkat表达特异性C1q受体,并对其特性进行了分析Jurkat可为C1q或抗人C1q受体抗体112识别,其对异硫氰酸荧光黄标记C1q的结合能被未标记C1q所抑制.在生理离子强度和温度条件下,Jurkat与125I-C1q的结合呈持异、剂量依赖、可饱和及可逆性,每个细胞C1q结合位点数为1.1×106,对C1q的Ka值为1.5×107mol-1,Hill系数为0.9643.JurkatC1q受体识别C1q的胶原样区.该受体是分子量约70000的膜蛋白分子

Thermodynamic data were determined for the reversible binding of O 2 to two compounds of dicobalt(II) di(meso tetra phenyl)porphyrin derivatives with different lengths of diamidoaliphatic bridge (abbreviated to Co 2PP 8 and Co 2PP 4) in N,N dimethylformamide at room temperature. The partial pressure of dioxygen necessary for half oxygenation ( P 1/2 ) and Hill coefficient ( n ) at 298 K were determined as follows: P 1/2 =54.2 kPa, n =2.0 for Co 2PP 8 and P 1/2 =6.8...

Thermodynamic data were determined for the reversible binding of O 2 to two compounds of dicobalt(II) di(meso tetra phenyl)porphyrin derivatives with different lengths of diamidoaliphatic bridge (abbreviated to Co 2PP 8 and Co 2PP 4) in N,N dimethylformamide at room temperature. The partial pressure of dioxygen necessary for half oxygenation ( P 1/2 ) and Hill coefficient ( n ) at 298 K were determined as follows: P 1/2 =54.2 kPa, n =2.0 for Co 2PP 8 and P 1/2 =6.8 kPa, n =1.8 for Co 2PP 4,respectively. The rate equations of reversible oxygen binding by Co 2PP 8 were determined and the reaction path was proposed. The results of thermodynamic and kinetic studies indicate that there exists strong cooperative effect during oxygenation of the compounds. The ESR observation reveals that the dioxygen complexes formed in the solutions are of superoxo (Co O - 2) type.

TheStrongCooperativityofDioxygenBindingbyDicobalt(I)DiporphyrinCompoundsinNonaqueousSolutionatRoomTemperatureZhouXiaohai,Den...

 
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