English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 60868/93650 (65%)
造访人次 : 1147085      在线人数 : 20
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻

    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/41230

    题名: Electrophoresis of biological cells:charge-regulation and multivalent counterions association model
    作者: Hsu, Jyh-ping;Hseih, Tien-Shiang;Young, Tai-Horng;曾琇瑱;Tseng, Shio-jenn
    贡献者: 淡江大學數學學系
    日期: 2003-04-01
    上传时间: 2010-01-28 07:01:20 (UTC+8)
    出版者: Wiley-Blackwell
    摘要: The electrophoresis of a biological cell is analyzed theoretically. An entity, which is of amphoteric nature, is used to simulate its electrophoretic behavior. To reflect conditions of practical interest, we assume that the liquid phase contains mixed (a:b)+(c:b) electrolytes, where a and c are the valences of cations, and b is the valence of anions. We consider the case where the surface of a cell contains both bivalent acidic and monovalent basic functional groups, the dissociation/association of them yields fixed surface charge, and the multivalent cations in the liquid phase are allowed to combine with dissociated acidic functional groups, which has the effect of lowering the charge density on cell surface. The electrophoretic behaviors of a cell under various conditions are illustrated. The results obtained can be used to identify the types of functional groups that may be present on cell surface. On the other hand, if the surface functional groups involved in cell electrophoresis are known, then their density and the associated dissociation/association constants can be estimated from experimental data.
    關聯: Electrophoresis 24(9), pp.1338-1346
    DOI: 10.1002/elps.200390172
    显示于类别:[數學學系暨研究所] 期刊論文


    档案 描述 大小格式浏览次数
    Electrophoresis of biological cells charge-regulation and multivalent counterions association model.pdf141KbAdobe PDF2检视/开启



    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - 回馈