54807
Mono Q® 5/50 GL
10 μm particle size, L × I.D. 5 cm × 5 mm
Sinônimo(s):
Amersham Biosciences Ion Exchange Columns
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About This Item
Código UNSPSC:
23151817
NACRES:
NA.56
Produtos recomendados
C × D.I.
5 cm × 5 mm
Nível de qualidade
Matriz
MonoBeads
Grupo ativo da matriz
quaternary amine
tamanho de partícula
10 μm
compatibilidade
mode of use ion exchange
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Descrição geral
Mono columns are highly efficient, pH-stable columns designed for high performance ion exchange separations of proteins, peptides, and polynucleotides, in applications including peptide mapping and monoclonal antibody purification. The unique properties of these columns are based on MonoBeads support – a beaded hydrophilic material with the narrowest particle size distribution of any chromatographic support. This monodispersity permits high flow rates at relatively low backpressures.
Mono columns are highly efficient, pH-stable columns designed for high performance ion exchange separations of proteins, peptides, and polynucleotides. The unique properties of these columns are based on MonoBeads support, a beaded hydrophilic material with the narrowest particle size distribution of any chromatographic support. This monodispersity permits high flow rates at relatively low backpressures.
Aplicação
Mono columns are used in applications including peptide mapping and monoclonal antibody purification. Mono Q columns have been used to develop a method for high-resolution analysis and purification of oligonucleotide dithioates and to investigate separation of DNA restriction fragments.
Informações legais
Mono Q is a registered trademark of Cytiva
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Xianbin Yang et al.
Analytical biochemistry, 306(1), 92-99 (2002-06-19)
A method using a strong anion-exchange liquid-chromatography column, Mono-Q, has been developed for high-resolution analysis and purification of oligonucleotide dithioates, which were synthesized by an automated, solid-phase, phosphorothioamidite chemistry. High-resolution separation of oligonucleotide phosphorodithioates from monothiophosphate impurities was obtained. High-resolution
E Westman et al.
Analytical biochemistry, 166(1), 158-171 (1987-10-01)
Separation of DNA restriction fragments by FPLC ion-exchange chromatography on Mono Q and Mono P columns was investigated. The columns were found to be particularly suitable for the separation of fragments up to 500-600 bp long. Larger fragments can also
Chromatograms
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