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大鼠脑组织蛋白质双向电泳技术的建立
引用本文:周成林,王继生,李惠芝,邱宗荫,宋敏.大鼠脑组织蛋白质双向电泳技术的建立[J].重庆医科大学学报,2006,31(6):794-797.
作者姓名:周成林  王继生  李惠芝  邱宗荫  宋敏
作者单位:1. 重庆医科大学药学院,重庆,400016
2. 重庆医科大学检验系,重庆,400016
摘    要:目的:建立大鼠脑组织蛋白质双向电泳技术。方法:利用不同体积的裂解液提取大鼠脑组织中的蛋白质,并通过不同的蛋白质上样量(1mg,2mg,3mg),进行双向电泳,考马斯亮蓝染色,图谱分析。结果:在等电点3~10,分子量6.5~200ku范围内分离得到蛋白质斑点为,1mg蛋白质上样量为546个蛋白质斑点,2mg为780个,3mg为805个斑点。2mg蛋白质上样量的双向电泳图谱更清晰,分离更好。结论:成功建立了大鼠脑组织蛋白质的双向电泳技术。

关 键 词:蛋白质组学  双向电泳  脑组织  裂解液
文章编号:0253-3626(2006)06-0794-04
收稿时间:05 16 2006 12:00AM
修稿时间:2006年5月16日

Establishment of a two-dimensional electrophoresis technology on brain tissue protein of rat
ZHOU Chenglin,et al.Establishment of a two-dimensional electrophoresis technology on brain tissue protein of rat[J].Journal of Chongqing Medical University,2006,31(6):794-797.
Authors:ZHOU Chenglin  
Affiliation:Department of Pharmaceutical Analysis, Pharmaceutial School, Chongqing Medical University
Abstract:Objective:To establish a two-dimensional electrophoresis technology on brain tissue protein of rat.Methods:Lysis buffer of different volume was taken to extract brain tissue proteins of rat,and different protein quantities(1mg,2mg,3mg) were taken to establish a two-dimensional electrophoresis.Coomassie brilliant blue was applied to stain protein,and patterns were analyzed.Results:With a molecular mass between 6.5~200ku and isoelectric points(pI) from 3~10,1mg proteins obtained 546 protein spots,2mg 780,and 3mg 805.Pattern of 2mg protein was the best.Conclusion:A two-dimensional electrophoresis technology on brain tissue protein of rat has been established successfully.
Keywords:Proteomics  Two-dimensional electrophoresis  Brain tissue  Lysis buffer
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