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- W2376152195 abstract "Objective: To obtain polycystin 1 intracellular region. Methods: cDNA of polycystin 1 intracellular region was generated by PCR and then cloned into pProEX Hta, which was prokaryotic expression vector. After verified by sequencing, the recombinant was transformed into E.coli host to express and purify the fusion protein by affinity chromatography. Results: 660 bp cDNA of polycystin 1 intracellular region and 2.6×10 4 fusion protein were obtained. Conclusion: The fusion protein containing polycystin 1 intracellular region is obtained and is helpful for preparing anti polycystin 1 monoclonal antibody. [" @default.
- W2376152195 created "2016-06-24" @default.
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- W2376152195 date "2001-01-01" @default.
- W2376152195 modified "2023-09-25" @default.
- W2376152195 title "Cloning and expression of polycystin-1 intracellular region cDNA" @default.
- W2376152195 hasPublicationYear "2001" @default.
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