English  |  正體中文  |  简体中文  |  Items with full text/Total items : 16714/19009 (88%)
Visitors : 5717209      Online Users : 61
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: http://ir.cnu.edu.tw/handle/310902800/30504


    標題: Remnant Cationic Dendrimers Block RNA Migration in Electrophoresis after Monophasic Lysis
    RNA純化經單相打碎後殘留之陽離子性樹枝體抑制電泳移動之影響
    作者: Yi-Lin Lin(林宜陵)
    Jung-Hua Steven Kuo(郭榮華)
    貢獻者: Graduate lnstitute of Pharmaceutical Sciences,Chia Nan University of Pharmacy and Science
    關鍵字: Cationic dendrimer
    RNA isolation
    DNA/dendrimer complexes
    Monophasic lysis
    Gel electrophoresis
    日期: 2008-07
    上傳時間: 2017-12-04 15:57:57 (UTC+8)
    摘要: Background and Purpose: Cationic dendrimers such as poly(amidoamine) (PAMAM) and poly(propyleneimine) (PPI) have attractive characteristics for the delivery of nucleic acid and various biomedical applications. Most studies have focused on cationic dendrimer-based intracellular delivery, and very few studies have focused on the non-specific interaction of remnant cationic dendrimers with total RNA after isolation directly from cells in vitro. Methods: We examined RNA isolation using the common method of monophasic lysis from human macrophage-like cells (U937) and mouse fibroblast cells (NIH/3T3) that had been exposed to dendrimers and DNA/dendrimer complexes using gel electrophoresis. Results: We found that PAMAM and PPI dendrimers strongly altered the mobility of RNA in the gels. In addition, the extent of dendrimer-induced alteration in RNA mobility was directly dendrimer-generation-dependent: the alteration was greater with higher-generation dendrimers. We also found that DNA/dendrimer complexes at higher dendrimer to DNA ratios interacted with RNA after isolation while gene expression was maintained. The interactions between RNA and remnant dendrimers after isolation were caused by electrostatic bindings, and we recovered total RNA using high ionic strength solvents (2M NaCl solution) to disrupt the electrostatic forces binding dendrimers to RNA. Conclusions: Because RNA isolation is routinely used for biological applications, such dendrimer-induced alteration in RNA mobility should be accounted for in the further processing of RNA-related applications.
    關聯: 第五屆海峽化學、生物及材料研討會,起迄日:2008/07/21-2008/07/22,地點:嘉南藥理科技大學
    Appears in Collections:[藥學系(所)] 會議論文
    [藥理學院] 2008第五屆海峽化學、生物及材料研討會

    Files in This Item:

    File Description SizeFormat
    B02.pdf390KbAdobe PDF12View/Open


    All items in CNU IR are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback