A life-cycle stage-specific antigen of Theileria parva recognized by anti-macroschizont monoclonal antibodies

Four monoclonal antibodies, raised against macroschizonts ofTheileria parva, were studied to characterize their antigen binding specificity. The indirect fluorescent antibody test showed that the antigen(s) recognized were present in the macroschizont stage of the parasite life-cycle but not in piro...

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Autores principales: Shapiro, S.Z., Fujisaki, K., Morzaria, S.P., Webster, P., Fujinaga, T., Spooner, P.R., Irvin, A.D.
Formato: Journal Article
Lenguaje:Inglés
Publicado: Cambridge University Press 1987
Materias:
Acceso en línea:https://hdl.handle.net/10568/29396
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author Shapiro, S.Z.
Fujisaki, K.
Morzaria, S.P.
Webster, P.
Fujinaga, T.
Spooner, P.R.
Irvin, A.D.
author_browse Fujinaga, T.
Fujisaki, K.
Irvin, A.D.
Morzaria, S.P.
Shapiro, S.Z.
Spooner, P.R.
Webster, P.
author_facet Shapiro, S.Z.
Fujisaki, K.
Morzaria, S.P.
Webster, P.
Fujinaga, T.
Spooner, P.R.
Irvin, A.D.
author_sort Shapiro, S.Z.
collection Repository of Agricultural Research Outputs (CGSpace)
description Four monoclonal antibodies, raised against macroschizonts ofTheileria parva, were studied to characterize their antigen binding specificity. The indirect fluorescent antibody test showed that the antigen(s) recognized were present in the macroschizont stage of the parasite life-cycle but not in piroplasm, kinete or sporozoite stages. Immunoblot analysis of macroschizont stage antigens suggested that all four antibodies recognized the same antigen. This was a molecule which varied in molecular mass between different parasite stocks, ranging from 68000 to 95000 Da. The antigen was localized by immunoelectron microscopy to the surface of the intracellular macroschizonts.
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spelling CGSpace293962024-11-15T08:52:01Z A life-cycle stage-specific antigen of Theileria parva recognized by anti-macroschizont monoclonal antibodies Shapiro, S.Z. Fujisaki, K. Morzaria, S.P. Webster, P. Fujinaga, T. Spooner, P.R. Irvin, A.D. theileria parva monoclonal antibodies antigens antibodies infectious diseases parasitology Four monoclonal antibodies, raised against macroschizonts ofTheileria parva, were studied to characterize their antigen binding specificity. The indirect fluorescent antibody test showed that the antigen(s) recognized were present in the macroschizont stage of the parasite life-cycle but not in piroplasm, kinete or sporozoite stages. Immunoblot analysis of macroschizont stage antigens suggested that all four antibodies recognized the same antigen. This was a molecule which varied in molecular mass between different parasite stocks, ranging from 68000 to 95000 Da. The antigen was localized by immunoelectron microscopy to the surface of the intracellular macroschizonts. 1987-02 2013-06-11T09:23:25Z 2013-06-11T09:23:25Z Journal Article https://hdl.handle.net/10568/29396 en Limited Access Cambridge University Press Parasitology;94: 29-37
spellingShingle theileria parva
monoclonal antibodies
antigens
antibodies
infectious diseases
parasitology
Shapiro, S.Z.
Fujisaki, K.
Morzaria, S.P.
Webster, P.
Fujinaga, T.
Spooner, P.R.
Irvin, A.D.
A life-cycle stage-specific antigen of Theileria parva recognized by anti-macroschizont monoclonal antibodies
title A life-cycle stage-specific antigen of Theileria parva recognized by anti-macroschizont monoclonal antibodies
title_full A life-cycle stage-specific antigen of Theileria parva recognized by anti-macroschizont monoclonal antibodies
title_fullStr A life-cycle stage-specific antigen of Theileria parva recognized by anti-macroschizont monoclonal antibodies
title_full_unstemmed A life-cycle stage-specific antigen of Theileria parva recognized by anti-macroschizont monoclonal antibodies
title_short A life-cycle stage-specific antigen of Theileria parva recognized by anti-macroschizont monoclonal antibodies
title_sort life cycle stage specific antigen of theileria parva recognized by anti macroschizont monoclonal antibodies
topic theileria parva
monoclonal antibodies
antigens
antibodies
infectious diseases
parasitology
url https://hdl.handle.net/10568/29396
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