首页 | 本学科首页   官方微博 | 高级检索  
     

蛋白酶K-Chelex100法提取肋软骨DNA技术的优化
引用本文:王会品,王孝力,杨巍,谢云铁,王晓伟,谢波. 蛋白酶K-Chelex100法提取肋软骨DNA技术的优化[J]. 中国法医学杂志, 2012, 27(1): 54-55
作者姓名:王会品  王孝力  杨巍  谢云铁  王晓伟  谢波
作者单位:1. 中山市公安局,广东中山528403;南方医科大学,广东广州510515
2. 中山市公安局,广东中山,528403
摘    要:目的优化蛋白酶K的用量和消化时间,用于提取肋软骨DNA。方法 30份肋软骨样本各取大小为0.2cm×0.3cm×0.4cm的软骨块5份,分别编为A~E组。采用不同蛋白酶K用量和消化时间的Chelex100方法,提取5组各30份软骨块DNA,进行DNA定量、采用Sinofiler试剂盒扩增后进行电泳检测,采用非参数检验法比较检验成功率。结果 A~E组样本中采用加入2μL蛋白酶K并消化30min的D组方法成功率最高(96.7%),组间差异具有统计学意义。结论采用蛋白酶K-Chelex100方法,选择加入2μL蛋白酶K,消化30min可有效提高肋软骨DNA分型检验成功率。

关 键 词:法医物证学  蛋白酶K  肋软骨

An optimized DNA extraction method for costal cartilage by using protinase K and chelex-100
Wang Huipin , Wang Xiaoli , Yang Wei , Xie Yuntie , Wang Xiaowei , Xie Bo. An optimized DNA extraction method for costal cartilage by using protinase K and chelex-100[J]. Chinese Journal of Forensic Medicine, 2012, 27(1): 54-55
Authors:Wang Huipin    Wang Xiaoli    Yang Wei    Xie Yuntie    Wang Xiaowei    Xie Bo
Affiliation:1/1.Bureau of public security of Zhongshan City,Guangdong Zhongshan 528403,China;2.Southern Medical Univisity,Guangzhou 510515,China)
Abstract:Objective To establish an optimized DNA extraction method for costal cartilage by adjusting the volume of proteinase K and digestion time.Methods DNA was isolated from 30 costal cartilages(0.2cm×0.3cm×0.4cm) of each group(A~E) with different volume of proteinase K and sample digestion time.The extracted DNA was quantified,and then amplified with the Sinofiler kit followed by electrophorese.Statistical analysis was carried out for different extraction methods.Results Compared with other treatments,it showed the highest successful rate(96.7%) with 2μL proteinase K and 30 mins’ digestion time at 56℃(group D).Differences between different groups were significant.Conclusion Proteinase K DNA extraction protocol,with 2μL proteinase K and 30 mins’ digestion time at 56℃,can isolate DNA from costal cartilage with higher efficiency.
Keywords:forensic biological evidence  protinase K  costal cartilage
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号