- 1、本文档共8页,可阅读全部内容。
- 2、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。
- 3、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载。
- 4、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
查看更多
poster讲课幻灯片
Made by Group2 We divided our article into six section, including abstract, introduction, methods, discussion and reference. According to six section, we will introduce our poster completely . Conclusion: In this study we report the water stress induced protein aggregation and its abrogation followed by expression of group 1 and group 2 LEA proteins of water soluble proteomes in horsegram Discussion:The role of LEA proteins in relation to protein aggregation during water stressed conditions was discussed Result: We found no cross reaction of LEA 1 with proteome of 48 h stressed embryonic axis and 72 h stressed root and shoot samples. However, LEA 2 antibodies were cross reacted with four polypeptides with different molecular mass in shoot tissue samples and found no reaction with root proteome as evidenced from immuno-blot analysis. Method: Tissue-speci?c expression of LEA 1 protein decreased in the embryonic axis when compared to cotyledons in 24 h stressed seedlings. Abstract Introduction Method and materials 1. Plant material and stress treatments 2. Relative water content 3. Protein extraction and estimation 4. Protein aggregation 5. Electrophoresis 6. Protein gel blot analy Result 1. Expression of group 1 LEA proteins 2.Expression of group 2 LEA proteins Discussion In summary, we presented data on the developmentally regulated tissue speci?c expression of LEA 1 and 2 proteins under different levels of water stress in horsegram. From these results we hypothesize that the reduced protein aggregation and water stress induced accumulation of proteins could perhaps be due to high expression of LEA proteins particularly LEA 1 and 2 which are t
文档评论(0)