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Prokaryotic expression, purification, and identification of GST-β-catenin-His double labeled fusion protein

  • YIN Hui-Long ,
  • YUAN Li
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  • College of Life Sciences, Graduate University, Chinese Academy of Sciences, Beijing 100049, China

Received date: 2011-11-10

  Revised date: 2012-01-13

  Online published: 2012-11-15

Abstract

The cDNA sequence of β-catenin was amplified through RT-PCR with 6xHis tag added in the gene downstream, cloned into the vector pGEX-4T-1. The plasmid transformed into BL21pLysS was induced by IPTG. The induced fusion protein was purified stepwise using Glutathione Sepharose 4B and Ni columns. The final protein ran on SDS-PAGE with a specific band at the expected size of 114 kDa. Western Blotting showed that the purified protein can be recognized by the anti-β-catenin, anti-GST, and anti-His antibodies, respectively. All these results provide a basis for further study of β-catenin function.

Cite this article

YIN Hui-Long , YUAN Li . Prokaryotic expression, purification, and identification of GST-β-catenin-His double labeled fusion protein[J]. Journal of University of Chinese Academy of Sciences, 2012 , (6) : 847 -852 . DOI: 10.7523/j.issn.2095-6134.2012.6.019

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