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Expression and Characterization of alpha-Methylacyl CoA Racemase from Anisakis simplex Larvae
Artículo en Inglés | WPRIM (Pacífico Occidental) | ID: wpr-146175
Biblioteca responsable: WPRO
ABSTRACT
Larval excretory-secretory products of Anisakis simplex are known to cause allergic reactions in humans. A cDNA library of A. simplex 3rd-stage larvae (L3) was immunoscreened with polyclonal rabbit serum raised against A. simplex L3 excretory-secretory products to identify an antigen that elicits the immune response. One cDNA clone, designated as alpha-methylacyl CoA racemase (Amacr) contained a 1,412 bp cDNA transcript with a single open reading frame that encoded 418 amino acids. A. simplex Amacr showed a high degree of homology compared to Amacr orthologs from other species. Amacr mRNA was highly and constitutively expressed regardless of temperature (10-40degrees C) and time (24-48 hr). Immunohistochemical analysis revealed that Amacr was expressed mainly in the ventriculus of A. simplex larvae. The Amacr protein produced in large quantities from the ventriculus is probably responsible for many functions in the development and growth of A. simplex larvae.
Asunto(s)

Texto completo: Disponible Base de datos: WPRIM (Pacífico Occidental) Asunto principal: Filogenia / Inmunohistoquímica / Datos de Secuencia Molecular / Análisis por Conglomerados / Biblioteca de Genes / Secuencia de Aminoácidos / Clonación Molecular / Homología de Secuencia de Aminoácido / Anisakis / Racemasas y Epimerasas Límite: Animales / Humanos Idioma: Inglés Revista: The Korean Journal of Parasitology Año: 2012 Tipo del documento: Artículo
Texto completo: Disponible Base de datos: WPRIM (Pacífico Occidental) Asunto principal: Filogenia / Inmunohistoquímica / Datos de Secuencia Molecular / Análisis por Conglomerados / Biblioteca de Genes / Secuencia de Aminoácidos / Clonación Molecular / Homología de Secuencia de Aminoácido / Anisakis / Racemasas y Epimerasas Límite: Animales / Humanos Idioma: Inglés Revista: The Korean Journal of Parasitology Año: 2012 Tipo del documento: Artículo
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