1000 resultados para antisérum polyclonal SA
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Comprend : Déclaration de Pierre Calas. [À Châtelaine, 23 juillet 1762.]
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Comprend : Dépêche de Lord Whitworth, ambassadeur d'Angleterre en France, au cabinet britannique (Lord Hawkesbury) ; Déclaration adressée au ministre des Etats-Unis, ainsi qu'aux autres ministres et agens de puissances neutres, près le Gouvernement britannique ; Décret de Berlin, en notre camp impérial de Berlin ; Ordre du Conseil britannique ; Ordre du Conseil britannique ; Décret de Milan, en notre palais royal de Milan ; Ordre du Conseil britannique ; Ordre du Conseil britannique ; Rapport adressé à l'Empereur Napoléon par son ministre des relations extérieures / et communiqué au Sénat françois, dans la séance du 10 mars 1812 ; Déclaration du Gouvernement britannique ; Extrait du Traité de navigation et de commerce ; Extrait du Traité maritime conclu entre la Russie et l'Angleterre ; Déclaration de S. M. l'Impératrice de toutes les Russies aux Cours de Londres, de Versailles, et de Madrid ; Extrait de la déclaration de S. M. l'Empereur de toutes les Russies, publiée à St. Petersbourg
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Titre original : Reise um die Welt in den Jahren 1803, 1804, 1805 und 1806, auf Befehl seiner... Majestät Alexander des Ersten auf den Schiffen "Nadeshda" und "Newa"
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Collection : Les archives de la Révolution française ; 8.1033
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Congrès de la Société Française de Pédiatrie et de l'Association des Pédiatres de Langue Française (APLF)
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Collection : Science et religion ; 580
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The objective of this work was to produce and characterize specific antisera against Brazilian isolates of Grapevine leafroll-associated virus 2 (GLRaV-2) and Grapevine virus B (GVB), developed from expressed coat proteins (CPs) in Escherichia coli, and to test their possible use for the detection of these two viruses in diseased grapevines. The coat protein (CP) genes were RT-PCR-amplified, cloned and sequenced. The CP genes were subsequently subcloned, and the recombinant plasmids were used to transform E. coli cells and express the coat proteins. The recombinant coat proteins were purified, and their identities were confirmed by SDS-PAGE and Western blot and used for rabbit immunizations. Antisera raised against these proteins were able to recognize the corresponding recombinant proteins in Western blots and to detect GLRaV-2 and GVB in infected grapevine tissues, by indirect ELISA, discriminating healthy and infected grapevines with absorbances (A405) of 0.08/1.15 and 0.12/1.30, respectively. Expressing CP genes can yield high amount of viral protein with high antigenicity, and GLRaV-2 and GVB antisera obtained in this study can allow reliable virus disease diagnosis.
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Coordinated interactions between T and B cells are crucial for inducing physiological B cell responses. Mutant mice in which tyrosine 136 of linker for activation of T cell (LAT) is replaced by a phenylalanine (Lat(Y136F)) exhibit a strong CD4(+) T cell proliferation in the absence of intended immunization. The resulting effector T cells produce high amounts of T(H)2 cytokines and are extremely efficient at inducing polyclonal B cell activation. As a consequence, these Lat(Y136F) mutant mice showed massive germinal center formations and hypergammaglobulinemia. Here, we analyzed the involvement of different costimulators and their ligands in such T-B interactions both in vitro and in vivo, using blocking antibodies, knockout mice, and adoptive transfer experiments. Surprisingly, we showed in vitro that although B cell activation required contact with T cells, CD40, and inducible T cell costimulator molecule-ligand (ICOSL) signaling were not necessary for this process. These observations were further confirmed in vivo, where none of these molecules were required for the unfolding of the LAT CD4(+) T cell expansion and the subsequent polyclonal B cell activation, although, the absence of CD40 led to a reduction of the follicular B cell response. These results indicate that the crucial functions played by CD40 and ICOSL in germinal center formation and isotype switching in physiological humoral responses are partly overcome in Lat(Y136F) mice. By comparison, the absence of CD80-CD86 was found to almost completely block the in vitro B cell activation mediated by Lat(Y136F) CD4(+) T cells. The role of CD80-CD86 in T-B cooperation in vivo remained elusive due to the upstream implication of these costimulatory molecules in the expansion of Lat(Y136F) CD4(+) T cells. Together, our data suggest that CD80 and CD86 costimulators play a key role in the polyclonal B cell activation mediated by Lat(Y136F) CD4(+) T cells even though additional costimulatory molecules or cytokines are likely to be required in this process.