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• W2129311700 endingPage "449" @default.
• W2129311700 startingPage "432" @default.
• W2129311700 abstract "Isomaltose oligosaccharides varying in size from two sugars, isomaltose (IM2), to seven sugars, isomaltohepatose (IM7), were coupled to stearylamine by reductive amination with sodium cyanoborohydride. Each compound was purified by column chromatography to yield a series of glycolipids containing oligosaccharides differing in length. Stearyl-isomaltotriose to stearyl-IM7 could be incorporated into liposomes and could render them agglutinable by specific antibodies to alpha 1 leads to 6 dextran and could be lysed if complement was also added, whereas those containing stearyl-IM2 were not agglutinated or lysed, indicating that stearyl-IM2 may not be protruding from the liposome surface sufficiently to react with the antibody. Stearyl-isomaltosyl oligosaccharides by themselves or incorporated into liposomes were equally antigenic when emulsified in complete Freund's adjuvant. They elicited pauciclonal responses, and the antibodies were alpha 1 leads to 6 specific, cross-reacted with dextran, and gave semirestricted isoelectric focusing patterns." @default.
• W2129311700 created "2016-06-24" @default.
• W2129311700 creator A5058666321 @default.
• W2129311700 creator A5065494170 @default.
• W2129311700 date "1981-08-01" @default.
• W2129311700 modified "2023-09-24" @default.
• W2129311700 title "Immunochemical studies of conjugates of isomaltosyl oligosaccharides to lipid. I. Antigenicity of the glycolipids and the production of specific antibodies in rabbits." @default.
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• W2129311700 doi "https://doi.org/10.1084/jem.154.2.432" @default.
• W2129311700 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2186421" @default.
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• W2129311700 hasPublicationYear "1981" @default.
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