离子结合
- 与 离子结合 相关的网络例句 [注:此内容来源于网络,仅供参考]
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The results showed that Ti-bone tissue was integrated closely in a very reactive manner. Both physical and chemical integration occurred in the Ti-bone interface.
结果表明,纯钛种植体与骨结合十分紧密;钛与骨组织间的离子作用是相互的;钛—骨间既存在物理性结合,也存在化学性结合。
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The results show that this pyrano[4,3-b] pyran derivative observably quenches the fluorescence of BSA in a static quenching mode. The binding constants and the numbers of binding sites at different temperatures were obtained and the effects of some metal ions on the binding constant of the derivative and BSA were also discussed.
求得不同温度下二者的结合常数和结合位点数,探讨了微量金属离子对实验体系结合常数的影响,并根据热力学参数确定了这种吡喃并[4,3-b]吡喃衍生物与牛血清白蛋白之间的作用力类型。
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It is found that many factors in gelling, removing template and rebinding process such as pH values and ionic concentration etc. make an important influence on the parameters such as rebinding capacity and imprinting efficiency etc. of protein-imprinted hybrid microspheres.
研究还表明,凝胶化、洗脱和重结合过程中的诸多因素如pH值和离子强度等对蛋白质大分子印迹杂化聚合物微球的分子印迹特异重结合性参数如重结合容量和印迹效率等产生重要影响。
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As examples, The apparent binding constants of zinc ion with cysteine and tartaric acid system, and zinc with cysteine and lactic acid system have been obtained.
研究了三元相互竞争体系的毛细管电泳测定方法,测定了金属锌离子与酒石酸和半胱氨酸以及锌离于与乳酸和半胱氨酸两个三元结合体系的结合常数,并以此比较了两种锌形态与半胱氨酸结合能力的大小。
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Ca2+ and EGTA-containing gel electrophoresis, combined with the corresponding terbium fluorescence on the basis of selective occupation of calcium binding sites, were applied to identify the potential calcium binding domains in PS II particles.
采用含Ca2+和含EGTA的凝胶电泳,结合竞争性取代钙结合位点的钙离子的铽荧光的方法检测光系统II中的钙结合蛋白。
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However, only about one-third of the soluble calcium and magnesium is ionized, the remainder is bound to citrate, phosphate and bicarbonate in a number of complex undissociated ions, e.g.
然而实际上只有13的钙和镁以离子形式存在,蓁的全为部以复杂离子的形式与柠檬酸盐、磷酸盐和重碳酸协结合,如Ca柠檬酸盐离子
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However, only about one-third of the soluble ca lcium and magnesium is ionized, the remainder is bound to citrate, phosphate and bi ca rbonate in a number of complex undissociated ions, e.g.
然而实际上只有1\3的钙和镁以离子形式存在,蓁的全为部以复杂离子的形式与柠檬酸盐、磷酸盐和重碳酸协结合,如Ca柠檬酸盐离子
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The experiments confirm that Nuclear fast red bindto DNA to form a 1:1 association complex with the binding constant 7.29×10~5 L/mol,and the major binding mode of Nuclear fast red to DNA is electrostatic binding.However, at high iron strength, the major binding mode changes into intercalativebinding. Part four is about investigation on the interaction of purpurine with DNA.
结果显示,核固红与DNA主要以静电作用模式结合,结合位点为1,结合常数为7.29×10~5L/mol;而在高离子强度下,其主要作用模式改变为嵌插作用;第四部研究了红紫素与DNA的相互作用。
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It was observed that not only histidine, but also histidine-Co and histidine-Ni could induce and substitute some Cu and Zn from Cu_2Zn_2SOD, eventually influence the activity of this metalloenzyme. Histidine- metal ion complexes have stronger ability than histidine to displace the bound metal ion from SOD. In addition, the amount of foreign metal ion binding to the SOD was less than that of metal ion lost from SOD. It obviously means that there was apoenzyme in the solution.
实验结果表明: Cu2Zn2SOD酶不仅与组氨酸,而且还可以与组氨酸-CoⅡ)和组氨酸-Ni(Ⅱ相互作用,Cu2Zn2SOD酶中的部分Cu和Zn被诱导和置换出来,并相应地影响了酶的活性;组氨酸-金属离子配合物的作用比组氨酸强,酶活性降低也更明显;酶中结合的外来金属离子的量比从酶上被诱导和顶替下来的金属离子的量要少,说明在溶液中有脱辅基酶的存在。
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Er concentration.2. With the analysis of the optical parameters calculated by Judd-Ofelt theory and the lifetime of ~4I_(13/2) of Er gotten in experiment, we investigated Y dopings dispertion effect and influence to the environment of Er .3. In the research of Er/Yb/Al co-doped laser glass, we fixed the Er:Yb at 1:6 and varied the Al concentration.
我们利用Judd-Ofelt理论,计算得到了Er/Y共掺玻璃的Judd-Ofelt强度系数、光谱质量因子、自发辐射弛豫率和能级寿命等光谱参数,并且给出了不同Y掺杂浓度下Er~(3 )离子的荧光量子效率;结合Er~(3 )离子~4I_(13/2)能级的荧光寿命,深入探讨了掺Y对高浓度Er~(3 )离子在硼硅酸盐玻璃中分布的弥散作用和对配位场环境的影响。
- 推荐网络例句
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This one mode pays close attention to network credence foundation of the businessman very much.
这一模式非常关注商人的网络信用基础。
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Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.
扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。
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There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.
双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。