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小鼠Foxp3片段的表达和多克隆抗体的制备

Expression of Mouse Foxp3 Fragment and Preparation of Polyclonal Antibody Against Foxp3

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【作者】 王弘珺王颖超夏雪培彭建霞谭获赵勇

【Author】 WANG Hong-jun1 WANG Ying-chao2 XIA xue-pei3 PENG Jian-xia1 TAN Huo2 ZHAO Yong 1 (1 State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, The Chinese Academy of Sciences Beijing 100080, China) (2 The First Affiliated Hospital, Guangzhou Medical College Guangzhou 510182, China) (3 Endocrine Department, Beijing Haidian Hospital Beijing 100080, China)

【机构】 中国科学院动物研究所生物膜与膜生物工程国家重点实验室广州医学院第一附属医院血液科北京海淀医院内分泌科中国科学院动物研究所生物膜与膜生物工程国家重点实验室 北京100080广州510182北京100080北京100080

【摘要】 克隆了小鼠Foxp3片段,采用基因重组方法,构建重组表达载体pGEX4T1Foxp3。应用在大肠杆菌BL21(DE3)中诱导产生的GSTFoxp3融合蛋白免疫家兔,制备兔抗Foxp3多克隆抗体。经过ELISA检测,抗血清的效价达1∶128000;采用Westernblot检测,转染Foxp3MIGR载体的Ψam细胞中表达Foxp3蛋白,而仅转染MIGR空载体的Ψam细胞中为阴性表达,表眀抗体具有特异性。

【Abstract】 The pGEX-4T-1-Foxp3 expression vector has been constrncted with mouse Foxp3 fragment. The rabbit antibody against Foxp3 was obtained by immunizing a rabbit with GST-Foxp3 fusion protein expressed in E.coli. After the last immunization, the titer of antiserum against Foxp3 was about 1∶128 000 determined by ELISA. To identify the specificity of antibody, the Ψam cells were transfected with either Foxp3 MIGR or MIGR vector. Foxp3 protein was only detected by Western blot analysis in Ψam cells transfected with Foxp3 MIGR vector, but not in cells transfected with the control vector. It was shown that the antibody was specific for Foxp3 protein.

【基金】 中国科学院引进海外杰出人才百人计划资助项目(2003年85号);国家重点基础研究发展计划资助项目(2003CB515501);国家杰出青年基金资助项目(30425026)
  • 【文献出处】 中国生物工程杂志 ,Progress In Biotechnology , 编辑部邮箱 ,2005年11期
  • 【分类号】Q813.2
  • 【被引频次】7
  • 【下载频次】173
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