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Development of analysis method of methylation level using Zn finger protein

Development of analysis method of methylation level using Zn finger protein
锌指蛋白甲基化水平分析方法的开发
批准号:
22656190
负责人:
IKEBUKURO Kazunori
金额:
$2.28万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Challenging Exploratory Research
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010 至 2011

项目摘要

项目成果

IKEBUKURO Kazunori的其他基金

相关文献

中文摘要
翻译
我们的目的是开发利用甲基化DNA结合蛋白(MBD)和锌指蛋白融合荧光素酶分析DNA甲基化水平的方法(Zif-荧光素酶),并进行如下研究; 1)建立了一种利用MBD和Zif荧光素酶分析DNA甲基化水平的新方法。3)成功地进行了雄激素受体基因区DNA甲基化水平的分析。我们还成功地分析了抑制癌变的p16基因区域的DNA甲基化水平。因此,我们可以说,我们的方法有望广泛应用于各种目标基因区域的DNA甲基化分析。
英文摘要
We aimed to develop the method to analyze the DNA methylation level using Methylated DNA Binding protein(MBD) and Zinc finger protein fused luciferase(Zif-luciferase) and carried out the research as follows;1) We developed the novel method for analyzing the DNA methylation level using MBD and Zif-luciferase.2) We designed and constructed the novel Zif-luciferase which enable us the analysis of DNA methylation level of the gene region of androgen receptor which relates to the canceration.3) We succeed in the analysis of the DNA methylation level Zif-luciferase. We also succeed in the analysis of the DNA methylation level of the p16 gene region which suppressing canceration. Therefore we can say our method is expected for broad application of the DNA methylation analysis of various target gene region.
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DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [池袋一典, 毛塚麻希, 平岡大介, 村上慶行, 志村宣明]
通讯作者: 志村宣明
メチル化CpG結合タンパク質を用いた新規メチル化頻度評価法の開発
使用甲基化 CpG 结合蛋白开发新的甲基化频率评估方法
DOI: --
发表时间: 2010
期刊:
影响因子: --
作者: [池袋一典, 他]
通讯作者: 他
Detection system using elecrochemical glucose sensor system and the change of nano-structure of aptamers
  • 批准号:
    24656499
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
  • 资助金额:
    $2.58万
  • 财政年份:
    2012
  • 负责人:
    IKEBUKURO Kazunori
  • 依托单位:
Development of simultaneous screening methods of aptamers which specifically recognize marker proteins for diseases
Design and expression of novel zinc finger protein for the detection of the DNA of pathogenic bacteria