期刊文献+

复合扩增18个基因座的初步研究 被引量:3

A study on co-amplification of the 18 CODIS STR Loci
下载PDF
导出
摘要 目的建立五色荧光18个基因座的复合扩增检验体系。方法设计、合成引物,通过调整引物浓度和复合扩增条件,建立起五色荧光复合扩增体系,包含Amelogen、D6S1043、D21S11、D7S820、CSF1PO、D2S1338、D3S1358、D13S317、D8S1179、D16S539、PentaE、TH01、TPOX、PentaD共计18个基因座。结果该复合扩增系统检验结果稳定,分型准确。结论五色荧光18个基因座复合扩增系统构建成功。 A study of 18-1oci multiplex was carried out on the co-amplification of seventeen STR loci plus the gender-determining locus Amelogen in a single amplification/detection of all CODIS (Combined DNA Index System) STR loci (CSF1PO, D3S1358,DSS818,D7S820,D8S1179,D13S317,D16S539,D18S51,D21S11,FGA,TH01,TPOX,and vWA) as well as four widelyaccepted STRs (D6S1043, PentaE,PentaD and D2S1338). By using five-dye fragment analysis technology and previously optimized DNATyperTM15 kit primer sequences, the results showed the multiplex sucessfully co-amplify and simultaneously detect all 18 loci and the multiplex could be a useful tool for forensic evidence testing.
出处 《刑事技术》 2007年第5期7-8,共2页 Forensic Science and Technology
基金 科技部863计划项目(2006AA020903) 十五攻关项目(2005BA801B12)
关键词 法庭科学 DNATyperTM15 五色荧光检测 DNA分型 forensic science DNATyper^TM15 five-dye fragment analysis technology DNA Typing
  • 相关文献

参考文献3

二级参考文献10

  • 1刘秋玲 吕德坚 伍新尧 等.亲子鉴定中2个STR基因座突变1例[J].中国法医学杂志,2001,16(4):238-239.
  • 2DNA recommendations.Report concerning further recommendations of the DNA Commission of the ISFH regarding PCR-based polymorphisms in STR (short tandem repeat)systems[J].Int J Leg Med,1994,107:159-160.
  • 3Bar W,Brinkmann B,Budowle B,et al.DNA recommendations:Further report of the DNA Commission of the ISFH regarding the use of the short tandem repeat systems[J].Int J Leg Med,1997,110:175-177.
  • 4Jones D A.Blood samples:Probability of discrimination[J].J Forensic Sci Soc,1972,12:355-359.
  • 5Brenner C,Morris J.Paternity index calculations in single locus hypervariable DNA probes:Validation and other studies,In proceedings for the International Symposium on Human Identification1989[Z].Promega Corporation Madisom WI.1990,21-53.
  • 6Botstein D,White R L,Skolnick M,et al.Construction of a genetic linkage map in using restriction fragment length polymorphisms[J].Am J Hum Genet,1980,32:314 -331.
  • 7刘雅诚,霍振义,唐晖,杨剑,贾淑琴,马万山,焦章平.北京汉族群体9个STR位点的频率分布及法医学应用[J].中国法医学杂志,1998,13(4):210-212. 被引量:33
  • 8余纯应,杨庆恩,陈慧,杨荣芝.10个STR座位的法医学应用回顾[J].同济医科大学学报,1999,28(3):214-217. 被引量:6
  • 9刘超,李越,王穗保,刘长晖,刘宏,陈晓晖.广州地区汉族人群PentaD及PentaESTR基因座频率[J].中国法医学杂志,2001,16(3):164-165. 被引量:9
  • 10庾蕾,伍新尧,黄艳梅,蔡贵庆,许传超,童大跃.用荧光标记MVR-PCR方法研究中国汉族人群DYF155S1基因座多态性[J].Acta Genetica Sinica,2003,30(1):15-19. 被引量:12

共引文献25

同被引文献21

引证文献3

二级引证文献12

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