首页 | 本学科首页   官方微博 | 高级检索  
     

PCR方法在HSF1基因敲除小鼠基因型分析中的应用
引用本文:陈广文,刘喜玲,肖献忠. PCR方法在HSF1基因敲除小鼠基因型分析中的应用[J]. 中国实验动物学报, 2002, 10(2): 73-76
作者姓名:陈广文  刘喜玲  肖献忠
作者单位:1. 中南大学湘雅医学院病理生理学教研室,长沙,410078
2. 卫生部肝胆肠外科中心医学工程研究室
基金项目:国家自然科学基金“α- B晶状体蛋白保护心肌细胞缺氧损伤研究”(3 9770 3 0 7)
摘    要:目的 为HSF1基因敲除鼠探索快速、简单的基因型PCR检测方法。方法 设计两对引物扩增野生型HSF1基因和HSF1缺陷突变基因的DNA片段 ,用PCR仪梯度方案测试最佳退火温度 ,并将所得基因型结果与经典的Southernblot方法比较。结果 野生型仅在 5 6 2bp处有一条条带 ,突变纯合子仅在 377bp处有一条条带 ,杂合子则在377bp和 5 6 2bp处出现两条条带。用PCR方法获得的HSF1基因分析结果与经典的Southernblot方法获得的结果完全一致。结论 用PCR方法分析HSF1基因敲除鼠的基因型具有快速、简单、廉价和适用的特点

关 键 词:聚合酶链反应  基因型  Southernblot  基因打靶  热休克因子1
文章编号:1005-4847(2002)02-0073-04
修稿时间:2001-08-28

Genotype Analysis of HSF1 Gene Knockout Mice with Polymerase Chain Reaction
CHEN Guangwen,LIU Xiling,XIAO Xianzhong. Genotype Analysis of HSF1 Gene Knockout Mice with Polymerase Chain Reaction[J]. Acta Laboratorium Animalis Scientia Sinica, 2002, 10(2): 73-76
Authors:CHEN Guangwen  LIU Xiling  XIAO Xianzhong
Abstract:Objective This study was to explore a simple and quick polymerase chain reaction (PCR) method for the genotyping of heat shock factor 1(HSF1) knockout mice. Method Two pairs of primers were designed to amplify genomic DNA fragment of wild-type HSF1 gene and the same region on HSF1 targeting vector respectively. A gradient PCR strategy was used to test the best annealing temperature. Results A 562 bp band was found in wild-type HSF1 mice, a 377 bp band in homozygous mutated HSF1 mice and both bands in heterozygous mice. The genotyping results were completely coincided with those from typical Southern blot. Conclusion PCR is a simple, fast and practical method for the genotyping of HSF1 gene knockout mice.
Keywords:Polymerase Chain Reaction  genotype  Southern blot  gene targeting  Heat shock factor 1
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