Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/92671
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dc.contributor.authorZhang, B.-
dc.contributor.authorWang, Y.-
dc.contributor.authorGao, M.-
dc.contributor.authorGu, M.-
dc.contributor.authorWang, C.-
dc.date.issued2012-
dc.identifier.citationJournal of Separation Science, 2012; 35(12):1406-1410-
dc.identifier.issn1615-9306-
dc.identifier.issn1615-9314-
dc.identifier.urihttp://hdl.handle.net/2440/92671-
dc.description.abstractA new protein adsorbent is introduced based on the coupling of the common buffer ion, tris(hydroxymethyl)aminomethane, to the agarose gel Sepharose HPfrom GEHealthcare Bio-Sciences AB, Uppsala, Sweden. The article describes the synthesis of the new adsorbent and the use of BSA as a model in a binding study. By optimization of the coupling procedure, a maximum ligand density of 63.5 μmol/mL gel could be obtained. Adsorption equilibria were investigated in the pH range 5.0–8.0 and at salt concentrations of 0–0.4 mol/L. Binding of BSA under different conditions indicated that both electrostatic interaction and hydrogen bonding were involved in the adsorption process where the former played a major role.-
dc.description.statementofresponsibilityBin Zhang, Ye Wang, Min Gao, Ming Gu, and Changhai Wang-
dc.language.isoen-
dc.publisherWiley-VCH Verlag-
dc.rights© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim-
dc.source.urihttp://dx.doi.org/10.1002/jssc.201200118-
dc.subjectAdsorption equilibrium; Bovine serum albumin; Protein adsorption; Sepharose HP; Tris(hydroxymethyl)aminomethane-
dc.titleTris(hydroxymethyl)aminomethane-functionalized agarose particles: parameters affecting the binding of bovine serum albumin-
dc.typeJournal article-
dc.identifier.doi10.1002/jssc.201200118-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 7
Chemical Engineering publications

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