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Registro Completo |
Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
Data corrente: |
09/09/2021 |
Data da última atualização: |
09/09/2021 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
CRUZ NETO, A. J. da; ANDRADE, E. C. de; BARBOSA, C. de J.; SCHNADELBACH, A. S. |
Afiliação: |
ALÍRIO JOSE DA CRUZ NETO, UFS; EDUARDO CHUMBINHO DE ANDRADE, CNPMF; CRISTIANE DE JESUS BARBOSA, CNPMF; ALESSANDRA SELBACH SCHNADELBACH, UFBA. |
Título: |
Caracterização molecular de um isolado do Papaya meleira vírus 2 (PMeV2) oriundo da região Nordeste do Brasil. |
Ano de publicação: |
2020 |
Fonte/Imprenta: |
In: JORNADA CIENTÍFICA EMBRAPA MANDIOCA E FRUTICULTURA, 14., 2020. Ciência em tempos de crise: resumos. Cruz das Almas, BA: Embrapa Mandioca e Fruticultura, 2020. 112 p. il. |
Idioma: |
Português |
Thesagro: |
Doença de Planta; Mamão. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/225793/1/p7.pdf
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Marc: |
LEADER 00671nam a2200157 a 4500 001 2134158 005 2021-09-09 008 2020 bl uuuu u00u1 u #d 100 1 $aCRUZ NETO, A. J. da 245 $aCaracterização molecular de um isolado do Papaya meleira vírus 2 (PMeV2) oriundo da região Nordeste do Brasil.$h[electronic resource] 260 $aIn: JORNADA CIENTÍFICA EMBRAPA MANDIOCA E FRUTICULTURA, 14., 2020. Ciência em tempos de crise: resumos. Cruz das Almas, BA: Embrapa Mandioca e Fruticultura, 2020. 112 p. il.$c2020 650 $aDoença de Planta 650 $aMamão 700 1 $aANDRADE, E. C. de 700 1 $aBARBOSA, C. de J. 700 1 $aSCHNADELBACH, A. S.
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Embrapa Mandioca e Fruticultura (CNPMF) |
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| Acesso ao texto completo restrito à biblioteca da Embrapa Pecuária Sul. Para informações adicionais entre em contato com cppsul.biblioteca@embrapa.br. |
Registro Completo
Biblioteca(s): |
Embrapa Pecuária Sul. |
Data corrente: |
23/01/2019 |
Data da última atualização: |
23/01/2019 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
B - 1 |
Autoria: |
NICIURA, S. C. M.; CRUVINEL, G. G.; MORAES, C. V.; DONATONI, F. A. B.; MALAGO JUNIOR, W.; BENAVIDES, M. V.; CHAGAS, A. C. de S. |
Afiliação: |
SIMONE CRISTINA MEO NICIURA, CPPSE; Giovanna Gabrielle Cruvinel, UNICEP; Caroline Valério Moraes, UFSCar; FLAVIA ALINE BRESSANI DONATONI, CPPSE; WILSON MALAGO JUNIOR, CPPSE; MAGDA VIEIRA BENAVIDES, CPPSUL; ANA CAROLINA DE SOUZA CHAGAS, CPPSE. |
Título: |
PCR-based genotyping of SNP markers in sheep. |
Ano de publicação: |
2018 |
Fonte/Imprenta: |
Molecular Biology Reports, v. 45, n. 4, p. 651-654, Aug. 2018. |
DOI: |
https://doi.org/10.1007/s11033-018-4206-8 |
Idioma: |
Inglês |
Conteúdo: |
Single nucleotide polymorphisms (SNPs) are the main type of variation in genome, enabling them to be associated with traits of economic importance in livestock. Genome-wide association studies (GWAS) have led to the discovery of SNPs associated with desirable traits in sheep. However, in these studies, SNPs are genotyped by high-throughput methods in genome scale, which are expensive and require sophisticated equipment and analysis methods. Therefore, the goal of this study was to develop a reliable, rapid, and inexpensive polymerase chain reaction (PCR)-based method to genotype a medium number of animals for a few candidate SNPs previously associated with desirable phenotypes in sheep by GWAS, using markers associated with gastrointestinal nematode resistance as a model. DNA extracted from white-blood cells of 150 sheep was submitted to PCR amplification followed by agarose gel electrophoresis and determination of banding pattern. Tetra-primer ARMS-PCR was successfully optimized after changes in annealing temperature; annealing and extension times; concentration of MgCl2 and DNA; ratios of inner, outer, forward and reverse primer; and addition of adjuvants, for genotyping the OAR2_14765360, OAR6_81718546, OAR11_62887032, and OAR12_69606944 SNPs in sheep. An extensive optimization of tetra-primer ARMS-PCR resulted in a suitable, simple, cost-effective PCR-based method of genotyping four SNP markers previously detected by chip arrays. |
Palavras-Chave: |
PCR RFLP; Resistência nematódeo gastrintestinal; Tetra primer ARMS PCR. |
Thesagro: |
Marcador Molecular; Ovino. |
Thesaurus NAL: |
Genome. |
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
Marc: |
LEADER 02277naa a2200277 a 4500 001 2104694 005 2019-01-23 008 2018 bl --- 0-- u #d 024 7 $ahttps://doi.org/10.1007/s11033-018-4206-8$2DOI 100 1 $aNICIURA, S. C. M. 245 $aPCR-based genotyping of SNP markers in sheep.$h[electronic resource] 260 $c2018 520 $aSingle nucleotide polymorphisms (SNPs) are the main type of variation in genome, enabling them to be associated with traits of economic importance in livestock. Genome-wide association studies (GWAS) have led to the discovery of SNPs associated with desirable traits in sheep. However, in these studies, SNPs are genotyped by high-throughput methods in genome scale, which are expensive and require sophisticated equipment and analysis methods. Therefore, the goal of this study was to develop a reliable, rapid, and inexpensive polymerase chain reaction (PCR)-based method to genotype a medium number of animals for a few candidate SNPs previously associated with desirable phenotypes in sheep by GWAS, using markers associated with gastrointestinal nematode resistance as a model. DNA extracted from white-blood cells of 150 sheep was submitted to PCR amplification followed by agarose gel electrophoresis and determination of banding pattern. Tetra-primer ARMS-PCR was successfully optimized after changes in annealing temperature; annealing and extension times; concentration of MgCl2 and DNA; ratios of inner, outer, forward and reverse primer; and addition of adjuvants, for genotyping the OAR2_14765360, OAR6_81718546, OAR11_62887032, and OAR12_69606944 SNPs in sheep. An extensive optimization of tetra-primer ARMS-PCR resulted in a suitable, simple, cost-effective PCR-based method of genotyping four SNP markers previously detected by chip arrays. 650 $aGenome 650 $aMarcador Molecular 650 $aOvino 653 $aPCR RFLP 653 $aResistência nematódeo gastrintestinal 653 $aTetra primer ARMS PCR 700 1 $aCRUVINEL, G. G. 700 1 $aMORAES, C. V. 700 1 $aDONATONI, F. A. B. 700 1 $aMALAGO JUNIOR, W. 700 1 $aBENAVIDES, M. V. 700 1 $aCHAGAS, A. C. de S. 773 $tMolecular Biology Reports$gv. 45, n. 4, p. 651-654, Aug. 2018.
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Embrapa Pecuária Sul (CPPSUL) |
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