Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1251575 | Chemical Research in Chinese Universities | 2008 | 4 Pages |
Abstract
A DNA fragment encoding the intracellular part of tyrosine phosphatase RPTPα designated as RPTPα-2D gene was amplified by PCR from a human prostate cDNA library and cloned into the pT7 E. coli expression vector. The resulting plasmid pT7-RPTPα-2D was used to transform Rosetta DE3 E. coli cells. RPTPα-2D was predominately expressed in the insoluble inclusion body and was effectively purified using preparative electrophoresis gels. Polyclonal antibodies were obtained after immunization of a rabbit with purified RPTPα-2D. The antibodies displayed a high titer and sensitivity. This study thus provided a valuable tool for further researches on RPTPα.
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Authors
Yang CHEN, Su-juan YANG, Yao FU, Jia-peng WANG, Zhi-zhuang ZHAO, Xue-qi FU,