Abstract
The human granulocytic colony-stimulating factor (hG-CSF) acts mainly by promoting the maturation of granulocytes and stimulating their phagocytic and chemotactic activity. It has been used in the treatment of many diseases, in particular in neutropenic conditions. Here, we describe the purification process of the recombinant protein hG-CSF expressed in Pichia pastoris. The protein purification proved to be efficient using the nickel affinity chromatography method described in this chapter.
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This work was supported by University of São Paulo (USP) and by CAPES.
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Archangelo, B.S., de Sousa Russo, E.M. (2018). Purification Method for Recombinant hG-CSF by Affinity Chromatography. In: Picanço-Castro, V., Swiech, K. (eds) Recombinant Glycoprotein Production. Methods in Molecular Biology, vol 1674. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7312-5_16
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DOI: https://doi.org/10.1007/978-1-4939-7312-5_16
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