Abstract
AbstractIn affinity partitioning the effectivity of purification is a function of the number of binding sites of the protein and the dissociation constant of the ligand/protein complex. To design an optimal purification process a mathematical model has been developed. Taking formate dehydrogenase from Candida boidinii as an example these data were evaluated in single stage experiments and could be confirmed by affinity partition chromatography.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Berichte der Bunsengesellschaft für physikalische Chemie
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.