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Registros recuperados : 6 | |
2. | | MACHADO, M. A.; BAPTISTA, C. R.; CRISTOFANI, M.; CARVALHO, S. A.; TARGON, M. L. N. Atividade do laboratorio de Biotecnologia em citros do Centro de Citricultura do IAC. Laranja, Cordeiropolis, v.14, n.2, p.499-511, 1993. Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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5. | | SILVA-PINHATI, A. C.; BOSCARIOL-CAMARGO, R. L.; MALOSSO, A.; SOUZA, A. A. de; AMARAL, A. M. do; CARLOS, E. F.; FREITAS-ASTUA, J.; TAKITA, M. A.; TARGON, M. L. N. P.; MACHADO, M. A. ESTs of roots of different citrus species and differential expression of genes associated to drought tolerance. In: THE INTERNATIONAL CONFERENCE ON THE STATUS OF PLANT & ANIMAL GENOME RESEARCH, 16., 2008, San Diego. Final abstracts guide. San Diego: Illumina, 2008. Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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6. | | SILVA-PINHATI, A. C.; BOSCARIOL-CAMARGO, R. L.; MALOSSO, A.; SOUZA, A. A. de; AMARAL, A. M. do; CARLOS, E. F.; FREITAS-ASTUA, J.; TAKITA, M. A.; TARGON, M. L. N. P.; MACHADO, M. A. ESTs of roots of different citrus species and differential expression of genes associated to drought tolerance. In: INTERNATIONAL PLANT & ANIMAL GENOMES CONFERENCE, 17., 2009, San Diego, CA. [Proceedings...]. [S. l.: s.n.], 2009. W112 Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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Registros recuperados : 6 | |
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Registro Completo
Biblioteca(s): |
Embrapa Uva e Vinho. |
Data corrente: |
06/07/2022 |
Data da última atualização: |
06/09/2023 |
Tipo da produção científica: |
Artigo em Anais de Congresso |
Autoria: |
NICKEL, O.; FAJARDO, T. V. M.; TARGON, M. L. N. P.; MACHADO, M. A. |
Afiliação: |
OSMAR NICKEL, CNPUV; THOR VINICIUS MARTINS FAJARDO, CNPUV; M. L. N. P. TARGON, Centro Avançado de Pesquisa Tecnológica do Agronegócio de Citros Sylvio Moreira; M. A. MACHADO, Centro Avançado de Pesquisa Tecnológica do Agronegócio de Citros Sylvio Moreira. |
Título: |
Production and Use of Polyclonal Antibodies to the Coat Protein of Apple stem grooving virus expressed in Escherichia coli. |
Ano de publicação: |
2004 |
Fonte/Imprenta: |
Acta Horticulturae, v. 657, p. 35-40, ISHS 2004. |
Idioma: |
Inglês |
Conteúdo: |
The coat protein (cp) gene of Apple stem grooving Capillovirus was amplified by RT-PCR, cloned, sequenced and subcloned in the expression plasmid pMal-c2. The ASGV cp gene was expressed in E. coli as a fusion protein (fp) containing a fragment of E. coli maltose binding protein (MBP). Bacterial cells were disrupted by sonication and the ASGVcp/MBP-fp was purified by amylose resin affinity chromatography. Polyclonal antibodies from rabbits immunized with the fp, gave specific reactions to ASGV from several infected apple cultivars at dilutions of up to 1:2000 in indirect ELISA. The ASGVcp/MBP-fp reacted to antisera raised against it as well as to commercial antisera against ASGV virions in immunoblotting. These results are a fundamental contribution to the development of an efficient ASGVindexing of propagative and mother stock materials in Southern Brazil. |
Palavras-Chave: |
ASGV; Recombinant viral antigen. |
Thesagro: |
Elisa. |
Thesaurus NAL: |
Antibodies; Apples; Recombinant antigens. |
Categoria do assunto: |
F Plantas e Produtos de Origem Vegetal |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1144491/1/Nickel-ISHS-657-2003-p35-40.pdf
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Marc: |
LEADER 01541nam a2200217 a 4500 001 2144491 005 2023-09-06 008 2004 bl uuuu u00u1 u #d 100 1 $aNICKEL, O. 245 $aProduction and Use of Polyclonal Antibodies to the Coat Protein of Apple stem grooving virus expressed in Escherichia coli.$h[electronic resource] 260 $aActa Horticulturae, v. 657, p. 35-40, ISHS 2004.$c2004 520 $aThe coat protein (cp) gene of Apple stem grooving Capillovirus was amplified by RT-PCR, cloned, sequenced and subcloned in the expression plasmid pMal-c2. The ASGV cp gene was expressed in E. coli as a fusion protein (fp) containing a fragment of E. coli maltose binding protein (MBP). Bacterial cells were disrupted by sonication and the ASGVcp/MBP-fp was purified by amylose resin affinity chromatography. Polyclonal antibodies from rabbits immunized with the fp, gave specific reactions to ASGV from several infected apple cultivars at dilutions of up to 1:2000 in indirect ELISA. The ASGVcp/MBP-fp reacted to antisera raised against it as well as to commercial antisera against ASGV virions in immunoblotting. These results are a fundamental contribution to the development of an efficient ASGVindexing of propagative and mother stock materials in Southern Brazil. 650 $aAntibodies 650 $aApples 650 $aRecombinant antigens 650 $aElisa 653 $aASGV 653 $aRecombinant viral antigen 700 1 $aFAJARDO, T. V. M. 700 1 $aTARGON, M. L. N. P. 700 1 $aMACHADO, M. A.
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Embrapa Uva e Vinho (CNPUV) |
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