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Mipu1,一个新的心肌缺血相关基因的组织表达和亚细胞定位。

Tissue expression and subcellular localization of Mipu1, a novel myocardial ischemia-related gene.

机构信息

Laboratory of Shock, Department of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan, China.

出版信息

Braz J Med Biol Res. 2010 Jan;43(1):43-51. doi: 10.1590/s0100-879x2009005000010. Epub 2009 Jul 31.

Abstract

Myocardial ischemic preconditioning up-regulated protein 1 (Mipu1), a novel zinc finger protein, was originally cloned using bioinformatic analysis and 5' RACE technology of rat heart after a transient myocardial ischemia/reperfusion procedure in our laboratory. In order to investigate the functions of Mipu1, the recombinant prokaryotic expression vector pQE31-Mipu1 was constructed and transformed into Escherichia coli M15(pREP4), and Mipu1-6His fusion protein was expressed and purified. The identity of the purified protein was confirmed by mass spectrometry. The molecular mass of the Mipu1 protein was 70.03779 kDa. The fusion protein was intracutaneously injected to immunize New Zealand rabbits to produce a polyclonal antibody. The antibody titer was approximately 1:16,000. The antibody was tested by Western blotting for specificity and sensitivity. Using the antibody, it was found that Mipu1 was highly expressed in the heart and brain of rats and was localized in the nucleus of H9c2 myogenic cells. The present study lays the foundation for further study of the biological functions of Mipu1.

摘要

心肌缺血预处理上调蛋白 1(Mipu1)是一种新型锌指蛋白,最初是在我们实验室使用大鼠心脏短暂缺血/再灌注程序的生物信息学分析和 5'RACE 技术克隆的。为了研究 Mipu1 的功能,构建了重组原核表达载体 pQE31-Mipu1,并转化到大肠杆菌 M15(pREP4)中,表达并纯化了 Mipu1-6His 融合蛋白。通过质谱法确认了纯化蛋白的身份。Mipu1 蛋白的分子量为 70.03779 kDa。融合蛋白经皮内注射新西兰兔以产生多克隆抗体。抗体的效价约为 1:16000。通过 Western blot 测试了抗体的特异性和敏感性。使用该抗体发现 Mipu1 在大鼠的心脏和大脑中高度表达,并定位于 H9c2 成肌细胞的核内。本研究为进一步研究 Mipu1 的生物学功能奠定了基础。

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