期刊文献+

天青Ⅰ共振光散射法测定DNA 被引量:2

Determination of deoxyribo nucleic acid with azure I by reconance light scattering method
在线阅读 下载PDF
导出
摘要 基于脱氧核糖核酸(DNA)对混合有机染料天青Ⅰ的共振光散射增强效应,拟定了一种测定DNA的共振光散射法。在pH9.5~10.5的范围内,天青Ⅰ在299、355、400、570、630nm附近均有较弱的共振光散射信号,随着DNA的加入,共振光散射信号大大增强。在355nm处,其散射光增强强度与DNA质量浓度呈线性关系。其线性回归方程为ΔI=-96.62+606.6ρ,线性范围为0 20~0.60μg mL,相关系数r=0.9998,检出限为11.2μg L。该方法可应用于合成样品中DNA的测定。 The resonance light scattering(RLS) spectra of azure Ⅰ with deoxyribonucleic acid were studied. The RLS intensities were of azure Ⅰ was greatly enhanced by deoxyribonucleic acid in pH range of 9.5~10.5. There were resonance light scattering peaks at 299, 355, 400, 570 and 630 nm respectively.The enhanced intensity of RLS at 355 nm was proportional to the concentration of deoxyribonucleic acid. So a method of RLS for the determination of deoxyribonucleic acid was established. The linear equation for yDNA was ΔI=-96.62+606.6ρ(μg/mL). The linear range of the calibration curve was 0.20~0.60 μg/mL. The detection limit was 11.2 μg/L. This method was simple, rapid and was applied to the determination of DNA in synthetic samples with satisfactory results.
出处 《分析试验室》 CAS CSCD 北大核心 2004年第12期35-38,共4页 Chinese Journal of Analysis Laboratory
基金 湖南省自科基金资助项目(00JJY2084) 湖南省教育厅资助项目(03C611)
关键词 脱氧核糖核酸 天青Ⅰ 共振光散射法 Deoxyribonucleic acids Azure Ⅰ Resonance light scattering method
  • 相关文献

参考文献11

  • 1魏宁.信息技术教师应该读什么书(二) 计算机及信息技术发展史[J].中国信息技术教育,2009(15):91-93. 被引量:6
  • 2Huang C Z,Li K A,Tong S Y. Bull Chem Soc Jpn,1997,70:1843
  • 3Huang C Z,Li K A,Tong S Y. Anal Chem,1996,68:2259
  • 4Huang C Z,Ph D.Dissertation. Peking University,1996
  • 5Giles K L,Myers A. Nature(London),1965,(4979):93
  • 6Li Wenyou,Xu Jingou,Guo Xiangqun et al. Anal Lett,1997,30(3):527
  • 7Huang Chengzhi,Li Yuanfang,Liu Xidong. Anal Chim Acta,1998,375:89
  • 8Liu Ying,Mao Chunqi,Li Kean et al. Anal Chim Acta,1999,379:39
  • 9Li Yuanfang, Huang Chengzhi, Huang Xiahua et al. Anal Chem Acta, 2001,429(2):311
  • 10Li Yuanfng,Huang Chengzhi,Li Ming. Anal Chem Acta, 2002,452(2):285

共引文献5

同被引文献24

引证文献2

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部