期刊文献+

刺槐根系可溶性蛋白SDS-PAGE分离方法的改进 被引量:1

Methodological Improvement of Seperating Soluble Protein by SDS-PAGE from Robinia pseudoacacia Root
下载PDF
导出
摘要 在利用常规SDS-PAGE方法分离刺槐根系可溶性蛋白的过程中,将样品处理液中的SDS、β-巯基乙醇、丙三醇的含量均增加50%。这样改进后的方法得到了分离效果明显较常规方法好的电泳图谱。经分析得出:常规SDS-PAGE方法中样品处理液的SDS和β-巯基乙醇浓度不足以充分溶解刺槐根系中的可溶性蛋白,丙三醇的浓度也不足以将样品很好地沉聚于点样槽底部。该试验为植物组织可溶性蛋白的SDS-PAGE分离提供了一套效果较好的参考方法。 An improvement was made in the conventional method SDS-PAGE for separating soluble protein from the roots of Robinia pseudoacacia by increasing the content of SDS, β-mercaptoethanol and glycerine to 50%. The separating effect of improved method was much better than the conventional one. Causes of the improvement were discussed; in the conventional method, the concentrations of SDS and β-mercapto- ethanol were not high enough to completely dissolve the soluble protein, and the concentration of glycerine was also not high enough to precipitate the samp e,
出处 《西北林学院学报》 CSCD 北大核心 2011年第1期128-130,共3页 Journal of Northwest Forestry University
基金 国家自然科学基金项目(30671673)
关键词 刺槐根系 可溶性蛋白 SDS-PAGE 改进 Robinia pseudoacacia root soluble protein SDS-PAGE improvement
  • 相关文献

参考文献9

二级参考文献103

共引文献177

同被引文献20

  • 1徐竹筠,王彤宇,何美瑛,唐锡华.水稻离体体细胞胚与合子胚的某些生化特性的比较[J].植物生理学报(0257-4829),1995,21(1):95-102. 被引量:9
  • 2郭尧君,余添.阳极电泳和阴极电泳的快速半干新技术[J].生物化学与生物物理进展,1996,23(4):359-364. 被引量:11
  • 3彭方仁,王改萍,郭娟.银杏营养贮藏蛋白质的细胞学及生物化学分析[J].南京林业大学学报(自然科学版),2006,30(4):109-113. 被引量:8
  • 4ZIMMERMAN J L. Somatic embryogenesis: a model for early development in higher plants [J]. Plant Cell, 1993, 5: 1411- 1423.
  • 5ZENG F, ZHANG X, CHENG L, et al. A draft gene regulatory network for cellular totipotency reprogramming during plant somatic embryogenesis [J]. Genomics, 2007, 90 : 620-628,.
  • 6LIPPERT D, ZHUANG J, RALPH S, et al. Proteome analysis of early somatic embryogenesis in Picea glauea [J]. Proteomics, 2005, 5 (2): 461-473.
  • 7IMIN N, NIZAMIDIN M, DANIHER D, et al. Proteomie analysis of somatic embryogenesis in Medieago truncatula. Explant cultures grown under 6-benzylaminopurine and 1- naphthaleneaeetic acid treatments [J]. Plant Physiology, 2005, 137 (4): 1250-1260.
  • 8MARSONI M, BRACALE M, ESPEN L, et al. Proteomic analysis of somatic embryogenesis in Vitis vinifera [J]. Plant Cell Reports, 2008, 27 (2): 347-356.
  • 9PAN Z, GUAN R, ZHU S, et al. Proteomic analysis of somatic embryogenesis in Valencia sweet orange (Citrus sinensis Osbeck) [J]. Plant Cell Reports, 2009, 28 (2): 281-289.
  • 10LAI Z X, HE Y, CHEN Y T, et al. Molecular biology and proteomics during somatic embryogenesis in Dimocarpus longan Lour [J]. Acta Horticulturae, 2010, 863: 95-101.

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部