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6+1 STR试剂盒和电泳凝胶EX-Q20用于DNA快速检验 被引量:3

Rapid DNA Identification Using 6+1 STR Kit and EX-Q20 Electrophoresis
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摘要 目的建立快速个体识别STR分型方法。方法取采集于FTA上的血样200份,经打孔仪取等量血痕分别使用6+1 STR试剂盒结合新型毛细管电泳凝胶EX-Q20进行快速电泳分析和使用SinofilerTM试剂盒结合POP4胶进行电泳分析,比较两者所耗费时间和结果的差异。结果 6+1 STR试剂盒结合新型毛细管电泳凝胶能够得到全部分型结果且耗时较短。结论 6+1 STR试剂盒结合新型毛细管电泳凝胶进行STR分型,结果准确可靠,尤其适用于重特大案件中大量人员的排查、比对,能大大提高办案效率。 Objective To establish a rapid STR genotyping method for individual identification.Methods Two hundred blood samples from FTA were collected.Equal amount of blood were collected by puncher and analyzed using two methods(6+1 STR kit in combination with EX-Q20 electrophoresis and SinofilerTM kit in combination with POP4 electrophoresis).Consuming time and results of two methods were compared.Results 6+1 STR kit in combination with EX-Q20 electrophoresis method can obtain all genotyping results and be shorter time.Conclusion 6+1 STR kit in combination with EX-Q20 electrophoresis method is used to STR genotyping with accurate,reliable results and this new method is potential value in mass personnel investigation and comparison in major criminal cases.It also can raise the work efficiency.
出处 《法医学杂志》 CAS CSCD 2011年第6期444-446,共3页 Journal of Forensic Medicine
关键词 法医遗传学 短串联重复序列 个体识别 快速检验 forensic genetics STR individual identification rapid identification
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参考文献6

  • 1辛军国,梁伟波,吕梅励,杜宏,陈国弟,张林.5个STR基因座遗传多态性研究及复合扩增试剂盒的构建及应用[J].四川大学学报(医学版),2006,37(1):84-87. 被引量:3
  • 2Mercier B, Gaucher C, Feugeas O, et al. Direct PCR from whole blood, without DNA extraction[J]. Nucleic Acids Res, 1990,18(19) :5908.
  • 3周怀谷,夏子芳,陈荣华,陶莉,杨辉,吴微微,王林生,平原,郑卫国.快速个体识别STR分型技术[J].法医学杂志,2010,26(5):381-382. 被引量:3
  • 4Vallone PM, Hill CR, Butler JM. Demonstration of rapid multiplex PCR amplification involving 16 genetic loci[J]. Forensic Sci Int Genet, 2008,3 (1) : 42-45.
  • 5Hammond HA, Jin L, Zhong Y, et al. Evaluation of 13 short tandem repeat loci for use in personal identi- fication applications[J]. Am J Hum Genet, 1994,55 (1) : 175-189.
  • 6Yeung SH, Greenspoon SA, McGuckian A, et al. Rapid and high-throughput forensic short tandem repeat typ- ing using a 96-lane microfabricated capillary array elec- trophoresis microdevice[J]. J Forensic Sci, 2006,51 (4) : 740-747.

二级参考文献22

  • 1Butler JM. Forensic DNA Typing : Biology, Technology, and Genetics of STR Markers [M]. 2nd. Elsevier, 2005.
  • 2Vallone PM, Hill CR, Butler JM. Demonstration of rapid multiplex PCR amplification involving 16 genetic loci[J]. Forensic Sci Int Genet,2008,3(1 ):42-45.
  • 3Liu P, Seo TS, Beyor N, et al. Integrated portable polymerase chain reaction-capillary electrophoresis microsystem for rapid forensic short tandem repeat typing[J]. Anal Chem,2007,79(5) : 1881-1889.
  • 4Liu P, Yeung SH, Crenshaw KA, et al. Real-time forensic DNA analysis at a crime scene using a portable microchip analyzer[J]. Forensic Sci Int Genet,2008,2(4): 301-309.
  • 5Yeung SH, Greenspoon SA, McGuckian A, et al. Rapid and high-throughput forensic short tandem repeat typing using a 96-lane microfabricated capillary array electrophoresis microdevice[J]. J Forensic Sci,2006,51 (4): 740-747.
  • 6Mercier B, Gaucher C, Feugeas O, et al. Direct PCR from whole blood, without DNA extraction[J]. Nucleic Acids Res, 1990,18(19) :5908.
  • 7Qin J, Fung Y, Lin B. DNA diagnosis by capillary electrophoresis and microfabricated eleetrophoretie devices[J]. Expert Rev Mol Diagn,2003,3(3):387-394.
  • 8Liu D, Zhou X, Zhong R, et al. Analysis of multiplex PCR fragments with PMMA microehip[J]. Talanta,2006, 68(3) :616-622.
  • 9Bar W,Brinkmann B,Lincoln P,et al.DNA recommendations-1994 report concerning further recommendations of the DNA Commission of the ISFH regarding PCR-based polymorphisms in STR (short tandem repeat) system.Int J Leg Med,1994;107(5) :159.
  • 10Bar W,Brinkmann B,Budowle B,et al.DNA recommendations:Further report of the DNA Commission of the ISFH regarding the use of short tandem repeat systems.Int J Leg Med,1997;110(4) :175.

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