Abstract
The 6xHis/Ni-NTA system allows rapid and efficient affinity purification of recombinant proteins from virtually any expression system. Protocols and tips for purification under both native and denaturing conditions are provided, as well as a rapid spin procedure for protein minipreps.
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Further Reading Reviews
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Kaslow, D. and Shiloach, J. (1994) Production, purification and immunogenicity of a malaria transmission-blocking vaccine candidate: TBV25H expressed in yeast and purified using Ni-NTA agarose.Bio/Technology 12, 494–499.
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Crowe, J., Masone, B.S. & Ribbe, J. One-step purification of recombinant proteins with the 6xHis tag and Ni-NTA resin. Mol Biotechnol 4, 247–258 (1995). https://doi.org/10.1007/BF02779018
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DOI: https://doi.org/10.1007/BF02779018