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- W2386076386 abstract "The full-length of L1 gene of HPV16 was amplified from cervical cancer tissue by PCR and inserted into pMD18T vector by T-A cloning.The cloned vector was confirmed by enzymes digestion and sequencing.The recombinant expression plasmid pGEX4T1-L1 was transformed into E.coli BL21 and induced by IPTG to express the target protein which was in a form of inclusion body.The target protein accounted for approximately 17% of total bacterial proteins.It could react with the serum of patients suffered from cervical cancer by Western blot analysis.The result showed that the recombinant prokaryotic expression vector pGEX4T1-L1 was successfully constructed and fusion protein was expressed in E.coli.It provided a basis for the investigation on the immune responses of L1 protein and potential development of vaccine." @default.
- W2386076386 created "2016-06-24" @default.
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- W2386076386 date "2007-01-01" @default.
- W2386076386 modified "2023-09-22" @default.
- W2386076386 title "Cloning and expression of L1 protein of human papillomavirus type 16(HPV16)" @default.
- W2386076386 hasPublicationYear "2007" @default.
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