These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: [Construction of the prokaryotic expression vector and expression of human CIDE-3 gene].
    Author: Yao L, Li Q, Li P, Zhang J, Ye J, Chen GS, Wang SF.
    Journal: Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi; 2006 Mar; 22(2):202-4. PubMed ID: 16507259.
    Abstract:
    AIM: To construct a prokaryotic expression vector for human CIDE-3 gene, and to express the gene in E.coli BL21(DE3). METHODS: The total RNA was extracted from human hepatocellular carcinoma cell line HepG2. CIDE-3 gene fragment was amplified by RT-PCR and was cloned into the pET28a(+) vector. The recombinant vector was identified by restriction endonuclease digestion analysis and DNA sequencing, and then it was transformed into E.coli BL21(DE3) through IPTG induction to express the target protein bearing His tag. RESULTS: A 516 bp of CIDE-3 gene fragment was obtained. After E.coli BL21(DE3) was transformed with recombinant vector pET28a(+)-CIDE-3 and through IPTG induction, the recombinant protein with relative molecular masse about 23,000 was obtained. SDS-PAGE analysis showed that the expressed product was mainly inclusion bodies, accounting for 32% of the total bacterial proteins. CONCLUSION: Recombinant expression vector pET28a(+)-CIDE-3 is constructed successfully. The expressed CIDE-3 protein will be helpful to our further research.
    [Abstract] [Full Text] [Related] [New Search]