2004
DOI: 10.1016/j.chroma.2003.10.041
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Contributions of commercial sorbents to the selectivity in immobilized metal affinity chromatography with Cu(II)

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Cited by 43 publications
(40 citation statements)
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“…Lou et al [25] prepared a GMA-co-EDMA monolith to which IDA was immobilised via the reactive epoxide moieties exposed at the monolith surface. Later in 2004, Ren et al [26] immobilised IDA on a GMA-co-EDMA monolith in a disk format (CIM Disk) for separation of histidine-containing peptides.…”
Section: Fabrication and Direct Visualisation Of Imac Stationary Phasmentioning
confidence: 99%
“…Lou et al [25] prepared a GMA-co-EDMA monolith to which IDA was immobilised via the reactive epoxide moieties exposed at the monolith surface. Later in 2004, Ren et al [26] immobilised IDA on a GMA-co-EDMA monolith in a disk format (CIM Disk) for separation of histidine-containing peptides.…”
Section: Fabrication and Direct Visualisation Of Imac Stationary Phasmentioning
confidence: 99%
“…This was followed by the addition of metal ions to this material to form coordination complexes for use in protein separations [88,89]. Similar supports have been placed in capillaries containing GMA/ EDMA monoliths for the separation of histidine-containing proteins by CEC [90].…”
Section: +mentioning
confidence: 99%
“…another study, four commercial IMAC columns charged with Cu 2+ and containing supports ranging from agarose to GMA/EDMA disks were compared in their isolation of histidine-tagged proteins for proteomics [89]. Cryogels containing IDA and Cu 2+ have been utilized to purify histidine-tagged lactate dehydrogenase [73] and Escherichia coli cells [74].…”
Section: Imacmentioning
confidence: 99%
“…Regarding new approaches one should also mention Convective Interaction Media monolithic discs (CIM discs) from BIASeparations, reported to enable immobilization of IDA [41], although the more elaborated larger scale modules are available for ionic and hydrophobic chromatography [38,42]. Currently the applicability of CIM disc monolythic columns for large scale cannot be yet fully assessed, however, good chemical stability, high resolution and especially low backpressure at high flow rates make this material promising for rapid purification of proteins especially when short residential time is needed.…”
Section: Reviewmentioning
confidence: 99%