Cloning, Optimization of Expression Condition and Purification of the Recombinant Nef- MPER-V3 Protein of HIV-1 in Prokaryotic Expression System

A. Faghih, S. M. Sadat, A. Bolhassani, S. Irani
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Abstract

a clear band of around 35 kDa in SDS-PAGE and was detectable using anti-Neff antibody in western blotting. Conclusion: Our results showed that the Nef-MPER-V3 protein was successfully expressed in prokaryotic system and purified protein may provide the antigen for future experiments for immunogenicity evaluation in mice is currently undertaken.
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HIV-1重组Nef- MPER-V3蛋白原核表达系统的克隆、表达条件优化及纯化
在SDS-PAGE中有一个约35 kDa的清晰条带,并在western blotting中使用抗内夫抗体检测到。结论:Nef-MPER-V3蛋白在原核系统中成功表达,纯化后的蛋白可为今后的小鼠免疫原性评价实验提供抗原。
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