Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies. Carbohydrate research [Carbohydr Res] Journal article | | Title | Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies. | | Author(s) | Fekete A, Borbás A, Antus S, Lipták A | | Institution | Research Group for Carbohydrates of the Hungarian Academy of Sciences, H-4010, Debrecen, PO Box 94, Hungary. | | Source | Carbohydr Res 2009 May 3. | | Abstract | Synthesis of tetra- and hexasaccharides built up from a beta-(1-->6)-linked galactopyranosyl backbone with arabinofuranosyl side chains at position 3 and with a 3-aminopropyl spacer related to arabinogalactans is described. These oligosaccharides were prepared for investigation of monoclonal antibodies raised against arabinogalactan proteins (AGPs) from pressed juice of Echinacea purpurea. | | Language | ENG | | Pub Type(s) | JOURNAL ARTICLE
| | PubMed ID | 19467537 |
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