中大機構典藏-NCU Institutional Repository-提供博碩士論文、考古題、期刊論文、研究計畫等下載:Item 987654321/71304
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 66984/66984 (100%)
造访人次 : 23046105      在线人数 : 322
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU 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: http://ir.lib.ncu.edu.tw/handle/987654321/71304


    题名: 使用不帶電中性核酸探針於矽奈米線場效電晶體檢測去氧核醣核酸與微核醣核酸之研究;Silicon nanowire field-effect biosensor for DNA and microRNA detection using neutralized-DNA (nDNA) probes
    作者: 蔡致勤;Tsai,Chih-Chin
    贡献者: 化學工程與材料工程學系
    关键词: 奈米場效電晶體;核醣核酸;微核醣核酸;Nano-wire Field effect transistor;DNA;micro-RNA
    日期: 2016-07-25
    上传时间: 2016-10-13 12:42:09 (UTC+8)
    出版者: 國立中央大學
    摘要: 在最近幾年,奈米場效電晶體已成為一個在生物醫學與檢測應用上面的強力工具。因為奈米場效電晶體有快速反應時間、高靈敏性、高專一性、體積小、即時偵測等優點。加上由於現行傳統的生物辨識技術如qPCR 及微陣列檢測基因序列,都須要加入螢光分子來標記這些生物分子,而奈米場效電晶體的非標定直接量測就可以避免因螢光標定等所造成之困擾。另外奈米場效電晶體的最低感測極限可以達到fM等級,因此已有相當多的研究團隊想利用此工具應用在感測基因序列上面並且希望藉由此能建立起一種較簡單的方法在重大疾病診斷上。然而這個方法在基因檢測上還是存在幾個難題。主要為溶液的離子強度會影響德拜長度(Debye length) ,並直接來影響奈米場效電晶體的感測。在本研究中我們專注在使用不帶電磷酸甲基化DNA(nDNA)探針來提升場效電晶體對DNA的感測還有探討相關的感測機制。不帶電磷酸甲基化DNA探針與目標核酸序列之間不存在靜電排斥力,因此造成不帶電磷酸甲基化DNA探針與目標核酸序列在低鹽濃度下,比帶電DNA探針容易地雜交形成雙股螺旋結構。我們也會設計部分修飾nDNA的探針來進一步增進奈米場效電晶體的檢測。從感測在不同鹽離子強度下、不同濃度的目標序列下還有非專一性控制組實驗,可以發現部分修飾nDNA的探針不僅能提高感測的靈敏度,還能增加與目標序列彼此之間的專一性。另外我們也會利用nDNA探針來檢測microRNA並探討與檢測DNA之間的不同。最後我們成功地架設奈米場效電晶體微陣列系統來檢測microRNA,並且從同一片晶片檢測不同序列的microRNA,我們可以看到奈米場效電晶體微陣列系統於檢測基因序列的可行性。;In recent years, nanowire field-effect transistor (NWFET) has been a powerful tool for the application of biomedical science, because its fast response time, high sensitivity and specificity, small size, real time detection, etc. And nowadays, conventional technics like qPCR microarray detects gene sequences, they need to add fluorescence to label the biomolecules. However,there is no use of labelling biomolecules in NWFET ,so it doesn’t have the side effect of labelling. In addition, the limit of detection (LOD) of NWFET can reach to femtomolar regime. So researchers want to apply it to gene sequencing and hope to find an easy way to disease diagnosis. While there are still some difficulties in this method, especially for DNA and microRNA detecting. In general, the main factor called Debye length mainly affect the sensing. In this study, we focus on using neutralized DNA (nDNA) probes which is uncharged to improve DNA detecting using FET biosensors and study the related mechanism. Neutralized DNA (nDNA) probes which is uncharged can form duplex with target sequence more easily than DNA probes in low salt concentration buffer, because there is less repulse force between the two sequences. We also designed some partially modified nDNA probes to improve our sensing. From the sensing in different ionic strength, different target concentrations sensing and non-specific control tests show that partially modified nDNA probes can not only enhance sensitivity but also improve specificity. In addition, we detect microRNAs using nDNA probes and find the difference between DNAs and microRNAs detecting. Finally, we successfully set up a SiNWFET microarray system to detect microRNAs. And from the experiments of sensing different microRNAs in one chip, we see the feasibility of detecting different microRNAs using SiNWFET microarray system.
    显示于类别:[化學工程與材料工程研究所] 博碩士論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML113检视/开启


    在NCUIR中所有的数据项都受到原著作权保护.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈  - 隱私權政策聲明