{"title":"Kohlenhydrate und Konjugate","description":"\u003cdiv id=\"loop-meta\" class=\"loop-meta-wrap pageheader-bg-stretch\"\u003e\n\u003cdiv class=\"hgrid\"\u003e\n\u003cdiv class=\"loop-meta  hgrid-span-12\" itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/WebPageElement\"\u003e\n\u003cdiv class=\"loop-description\" itemprop=\"text\"\u003e\n\u003cdiv class=\"term-description\"\u003e\n\u003cp\u003e\u003cstrong\u003eKohlenhydrate, Glykosidase-Inhibitoren, Endotoxin (synthetisch) und Glykopeptide.\u003c\/strong\u003e Seit fast einem halben Jahrhundert befasst sich das Peptid-Institut mit der Synthese biologisch aktiver Peptide mit variablen posttranslationalen Modifikationen. Glykopeptide gehören zu unserem Syntheserepertoire. Diese Glykopeptide enthalten eine Kohlenhydratkomponente, die an der Seitenkette von Serin, Threonin oder Asparagin eingeführt wird, was wiederum deren intrinsische Aktivität mehr oder weniger beeinflusst. Für die Synthese von Glykopeptiden ist sowohl das Wissen der Kohlenhydratchemie als auch das der Peptidchemie erforderlich. Die angebotenen Endotoxin-Reste werden unter Verwendung chemischer Methoden hergestellt und nicht aus biologischen Quellen isoliert. Daher ist bei der Verwendung von \u003cstrong\u003eLipid A\u003c\/strong\u003e oder \u003cstrong\u003eLipid IVA\u003c\/strong\u003e, die von PeptaNova angeboten werden, keine biologische Kontamination zu vermuten. Geschützte Galactose-, Glukose- und Mannose-Derivate sind nützliche Werkzeuge für die chemische Synthese von Kohlenhydraten.\u0026nbsp;\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv id=\"content-wrap\"\u003e\n\u003cdiv\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv class=\"berocket_lgv_widget\"\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003c\/div\u003e","products":[{"product_id":"acetofluoro-alpha-d-glucose-2-3-4-6-tetra-o-acetyl-alpha-d-glucopyranosyl-fluoride","title":"Acetofluoro-alpha-D-glucose\n2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl 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