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Updated: Jul 16, 2026
Determination of Immune Cell Identity and Purity Using Epigenetic-Based Quantitative PCR
Published on: February 19, 2020
[Cloning, expression and identification of human interleukin-10 gene]
1Department of Immunology, Beijing Institute of Infections Diseases, Beijing, China. energysj@yeah.net
Aim:
To construct a prokaryotic expression vector containing human interleukin-10 (IL-10) gene, express and identify the protein.
Methods:
Human IL-10 gene from HepG2 was isolated and identified by DNA sequencing, and then cloned into the expression vector PET-28 a (+) to construct prokaryotic expression vector. The recombinant protein was expressed in BL21(DE3) and identified by Western blot and ELISA.
Results:
The expressed protein was mainly located in the inclusion body. The relative molecular mass of the expressed product was identical to that of prediction. The expressed protein had binding activity with specific antibody.
Conclusion:
The human IL-10 gene was successfully cloned and expressed in E.coli. The expressed product had antigenicity which provides foundation for preparation of monoclonal antibodies against IL-10.
