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a bibo:Issue;
dcterms:medium ;
rdau:P60049 ;
rdau:P60050 ;
rdau:P60048 ;
dc:identifier "(DE-101)1328965295";
umbel:isLike , ;
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a bibo:Article;
dc:title "An antiserum which recognizes lipopolysaccharidereactive B cells in the mouse";
dcterms:creator _:node1jup961v3x58106520 .
_:node1jup961v3x58106520 gndo:preferredName "Forni, Luciana" .
marcRole:aut _:node1jup961v3x58106521 .
_:node1jup961v3x58106521 gndo:preferredName "Forni, Luciana" .
marcRole:aut _:node1jup961v3x58106522 .
_:node1jup961v3x58106522 gndo:preferredName "Coutinho, A." .
bibo:pageStart "56";
bibo:pageEnd "62";
dcterms:extent "7 S.";
dcterms:isPartOf ;
dcterms:description "Abstract: Rabbit antisera have been prepared against spleen B cells from C3H/Tif mice, high responders to lipopolysaccharide (LPS). After complete absorption on tissues of C3H/HeJ mice (LPS nonresponders), such antisera specifically stain and kill (in the presence of complement) a fraction of the B cells from a number of LPS high responder strains, and fail to recognize any cells in two different LPS nonresponder strains, C3H/HeJ and C57Bl/10.Sc.Cr. The ontogeny, organ and strain distribution of this B cell marker parallels LPS reactivity. Frequencies of cells stained by this antiserum correspond to the frequencies of LPS‐reactive B cell precursors recently determined. This antigen (s) is expressed by LPS‐activated B cell blasts but not by cells which remain small after 48 h in the presence of LPS. Removal of the cells recognized by the antisera leads to depletion of LPS‐reactive cells, while enriching for reactivity to another B cell mitogen, e.g. lipoprotein."@de;
dcterms:license ;
wdrs:describedby .
dcterms:license ;
dcterms:modified "2024-05-13T18:25:41.000"^^xsd:dateTime .
dcterms:issued "2005";
bibo:issue "8.2005, 1";
owl:sameAs .