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Coupling of m-aminophenyl boronate to the TSKgel 5PW polymeric support results in a ligand capable of forming a tetrahedral boronate anion under alkaline pH conditions. This anionic structure can bind with 1,2 cis-diol groups such as those found in carbohydrates, carbohydrate containing compounds and catecholamines. Interaction between the boronate anion and the 1,2 cis-diol groups is enhanced in the presence of Mg2+ ions and is inhibited by amine-containing buffers. Adsorption onto the TSKgel Boronate-5PW matrix takes place in basic buffers such as HEPES and morpholine while desorption takes place in carbohydrate or amine-containing mobile phase like sorbitol or Tris.
Applications include: nucleic acids, catecholamines, nucleosides and nucleotides. |
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Application |
Isocratic separation of nucleosides

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Ordering information: To place an order please contact Customer Service.
| P/N |
Description |
Pore size |
Particle size
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Dimension
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| 14449 |
TSKgel Boronate-5PW, Glass |
1,000 Å |
10 μm |
5 mm ID x 5 cm L
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| 13066 |
TSKgel Boronate-5PW |
1,000 Å |
10 μm |
7.5 mm ID x 7.5 cm L
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| 14451 |
TSKgel Boronate-5PW Glass Guardgel kit for P/N 14449 |
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20 μm |
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| 13125 |
TSKgel Boronate-5PW Guardgel kit for P/N 13066 |
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