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杜氏盐藻核基质的制备
引用本文:王天云,柴玉荣,侯卫红,谢华,赵青赞,王宁,薛乐勋.杜氏盐藻核基质的制备[J].郑州大学学报(医学版),2004,39(1):39-41.
作者姓名:王天云  柴玉荣  侯卫红  谢华  赵青赞  王宁  薛乐勋
作者单位:1. 郑州大学细胞生物学研究室,郑州,450052;新乡医学院细胞生物学教研室,新乡,453003
2. 郑州大学细胞生物学研究室,郑州,450052
基金项目:国家自然科学基金资助项目  3 0 2 70 0 3 1,国家高技术研究发展 ( 863 )计划  2 0 0 2AA62 80 5 0
摘    要:目的:制备盐藻核基质,进而分离核基质结合区(matrix attachment regions)。方法:采用体积分数0.5% TritonX—100破碎细胞,体积分数15%Percoll分离盐藻细胞核,二碘水杨酸锂(1ithium diiodosalicylate,LIS)抽提核蛋白,SDS—PAGE电泳分析蛋白质成分。结果:分离出了高纯度的盐藻细胞核,电泳分析表明绝大部分核蛋白已被去除。结论:体积分数0.5%TritonX—100能有效破碎盐藻细胞,体积分数15%Percoll可分离高纯度的盐藻细胞核,25mmol/L LIS抽提可除去盐藻绝大部分核蛋白获得核基质。

关 键 词:盐藻  核基质  核基质结合区  SDS—PAGE
修稿时间:2003年10月25

Preparation of nuclear matrix of Dunaliella salina
WANG Tianyun ,CHAI Yurong ,HOU Weihong ,XIE Hua ,ZHAO Qingzhan ,WANG Ning ,XUE Lexun Laboratory for Cell Biology,Zhengzhou University,Zhengzhou.Preparation of nuclear matrix of Dunaliella salina[J].Journal of Zhengzhou University: Med Sci,2004,39(1):39-41.
Authors:WANG Tianyun    CHAI Yurong  HOU Weihong  XIE Hua  ZHAO Qingzhan  WANG Ning  XUE Lexun Laboratory for Cell Biology  Zhengzhou University  Zhengzhou
Institution:WANG Tianyun 1,2),CHAI Yurong 1),HOU Weihong 1),XIE Hua 1),ZHAO Qingzhan 1),WANG Ning 1),XUE Lexun 1) 1)Laboratory for Cell Biology,Zhengzhou University,Zhengzhou 450052 2)Department of Cell Biology,Xinxiang Medical College,Xinxiang 453003
Abstract:Aim: Through preparing nuclear matrix of Dunaliella salina, in order to isolate the matrix attachment regions further.Methods: The D.salina cells were disrupted with 0.5%TritonX-100 and purified by centrifugation using 15% Percoll.The nuclear proteins were removed using 25 mmol/L lithium diiodosalicylate and the component of protein was analyzed by SDS-PAGE. Results: The pure nuclei of D.salina were isolated, and most protein component of nuclear protein was removed. Conclusion: The matrix of D.salina may be prepared through 25mmol/L LIS extracting nuclear protein.
Keywords:Dunaliella salina  nuclear matrix  matrix attachment region  SDS-PAGE
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