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Authordc.contributor.authorReyes Solovera, Mónica de los es_CL
Authordc.contributor.authorMedina, G. es_CL
Authordc.contributor.authorPalomino Mackenney, Jaime 
Admission datedc.date.accessioned2012-10-23T13:58:13Z
Available datedc.date.available2012-10-23T13:58:13Z
Publication datedc.date.issued2009-07
Cita de ítemdc.identifier.citationREPRODUCTION IN DOMESTIC ANIMALS Volume: 44 Pages: 350-353es_CL
Identifierdc.identifier.issn0936-6768
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/122442
General notedc.descriptionArtículo de Publicación ISIes_CL
Abstractdc.description.abstractAcrosin is an acrosomal protease synthesized as an inactive precursor, proacrosin, which is processed via autoproteolysis into active forms alpha- and beta-acrosin. In this paper, a comparative study on the immunoreactivity of acrosin during in vitro capacitation of frozen and fresh (control) canine sperm using Western blot analysis is reported. Semen samples were obtained by digital stimulation and ejaculates processed as fresh and frozen samples and then capacitated for 0, 30, 60 and 90 min. At each time period, samples were analyzed with monoclonal antibody C5F10 by Western blot. The antibody specifically recognized, in fresh and frozen/thawed spermatozoa, a 40-, 32- and 27-kDa bands corresponding to proacrosin, alpha- and beta-acrosin, respectively, during capacitation. Western immunoblots showed that the beta-acrosin reactivity in fresh sperm was directly proportional to the time of capacitation, whereas a decreased reactivity of active form of acrosin was observed with frozen-thawed sperm (p < 0.05). These results suggest that proacrosin is activated to beta-acrosin earlier in frozen/thawed dog spermatozoa than in fresh dog spermatozoa.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherWILEY-BLACKWELL PUBLISHING, INCes_CL
Keywordsdc.subjectZONA-PELLUCIDAes_CL
Títulodc.titleWestern Blot Analysis of Proacrosin/Acrosin in Frozen Dog Sperm During In Vitro Capacitationes_CL
Document typedc.typeArtículo de revista


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