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Registro Completo |
Biblioteca(s): |
Embrapa Unidades Centrais. |
Data corrente: |
05/12/2016 |
Data da última atualização: |
05/12/2016 |
Autoria: |
FLÓREZ, L. M. M.; BALLESTERO, H. F.; DUZANSKI, A. P.; BERSANO, P. R. O.; LIMA, J. F.; CRUZ, F. L.; MOTA, L. S.; ROCHA, N. S. |
Afiliação: |
LUIS M. M. FLÓREZ, UNESP/Universidade de Caldas; HALINE F. BALLESTERO, UNESP; ANDERSON P. DUZANSKI, UNESP; PAULO R. O. BERSANO, UECE; JOÃO F. LIMA, CEVAP/UNESP; FERNANDA L. CRUZ, UNESP; LÍGIA S. MOTA, UNESP; NOEME S. ROCHA, UNESP. |
Título: |
Immunocytochemical characterization of primary cell culture in canine transmissible venereal tumor. |
Ano de publicação: |
2016 |
Fonte/Imprenta: |
Pesquisa Veterinária Brasileira, Brasília, DF, v. 39, n. 9, p. 844-850, set. 2016. |
Idioma: |
Inglês |
Conteúdo: |
Immunochemistry with anti-vimentin, anti-lysozyme, anti-alpha 1 antitrypsin, anti-CD3 and anti-CD79α antibodies has been used for characterization of primary cell culture in the transmissible venereal tumor (TVT). Samples for primary cell culture and immunohistochemistry assays were taken from eight dogs with cytological and clinical diagnosis of TVT. To validate the immunochemical results in the primary cell culture of TVT, a chromosome count was performed. For the statistical analysis, the Mann-Whitney test with p<0.05 was used. TVT tissues and culture cells showed intense anti-vimentin immunoreactivity, lightly to moderate immunoreactivity for anti-lysozyme, and mild for anti-alpha-antitrypsin. No marking was achieved for CD3 and CD79α. All culture cells showed chromosomes variable number of 56 to 68. This is the first report on the use of immunocytochemical characterization in cell culture of TVT. Significant statistic difference between immunochemistry in tissue and culture cell was not established, what suggests that the use of this technique may provide greater certainty for the confirmation of tumors in the primary culture. This fact is particularly important because in vitro culture of tumor tissues has been increasingly used to provide quick access to drug efficacy and presents relevant information to identify potential response to anticancer medicine; so it is possible to understand the behavior of the tumor. |
Palavras-Chave: |
Alfa 1 antitripsina; Alpha 1 antitrypsin; Canine transmissible venereal tumo; Isozima; Tumor venéreo transmissível canino; Vimentina. |
Thesagro: |
Citogenética. |
Thesaurus Nal: |
Cytogenetics; Lysozyme; Vimentin. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/151255/1/Immunocytochemical-characterization.pdf
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Marc: |
LEADER 02414naa a2200325 a 4500 001 2057977 005 2016-12-05 008 2016 bl uuuu u00u1 u #d 100 1 $aFLÓREZ, L. M. M. 245 $aImmunocytochemical characterization of primary cell culture in canine transmissible venereal tumor. 260 $c2016 520 $aImmunochemistry with anti-vimentin, anti-lysozyme, anti-alpha 1 antitrypsin, anti-CD3 and anti-CD79α antibodies has been used for characterization of primary cell culture in the transmissible venereal tumor (TVT). Samples for primary cell culture and immunohistochemistry assays were taken from eight dogs with cytological and clinical diagnosis of TVT. To validate the immunochemical results in the primary cell culture of TVT, a chromosome count was performed. For the statistical analysis, the Mann-Whitney test with p<0.05 was used. TVT tissues and culture cells showed intense anti-vimentin immunoreactivity, lightly to moderate immunoreactivity for anti-lysozyme, and mild for anti-alpha-antitrypsin. No marking was achieved for CD3 and CD79α. All culture cells showed chromosomes variable number of 56 to 68. This is the first report on the use of immunocytochemical characterization in cell culture of TVT. Significant statistic difference between immunochemistry in tissue and culture cell was not established, what suggests that the use of this technique may provide greater certainty for the confirmation of tumors in the primary culture. This fact is particularly important because in vitro culture of tumor tissues has been increasingly used to provide quick access to drug efficacy and presents relevant information to identify potential response to anticancer medicine; so it is possible to understand the behavior of the tumor. 650 $aCytogenetics 650 $aLysozyme 650 $aVimentin 650 $aCitogenética 653 $aAlfa 1 antitripsina 653 $aAlpha 1 antitrypsin 653 $aCanine transmissible venereal tumo 653 $aIsozima 653 $aTumor venéreo transmissível canino 653 $aVimentina 700 1 $aBALLESTERO, H. F. 700 1 $aDUZANSKI, A. P. 700 1 $aBERSANO, P. R. O. 700 1 $aLIMA, J. F. 700 1 $aCRUZ, F. L. 700 1 $aMOTA, L. S. 700 1 $aROCHA, N. S. 773 $tPesquisa Veterinária Brasileira, Brasília, DF$gv. 39, n. 9, p. 844-850, set. 2016.
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Registro original: |
Embrapa Unidades Centrais (AI-SEDE) |
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Registro Completo
Biblioteca(s): |
Embrapa Soja; Embrapa Unidades Centrais. |
Data corrente: |
24/03/2011 |
Data da última atualização: |
14/10/2011 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
STOLF-MOREIRA, R.; LEMOS, E. G. de M.; ABDELNOOR, R. V.; BENEVENTI, M. A.; ROLLA, A. A. P.; PEREIRA, S. dos S.; OLIVEIRA, M. C. N. de; NEPOMUCENO, A. L.; MARCELINO-GUIMARÃES, F. C. |
Afiliação: |
RENATA STOLF-MOREIRA, UNESP Jaboticabal; ELIANA GERTRUDES DE MACEDO LEMOS, UNESP Jaboticabal; RICARDO VILELA ABDELNOOR, CNPSO; MAGDA APARECIDA BENEVENTI, UFRGS; AMANDA ALVES PAIVA ROLLA, UEL; SELMA DOS SANTOS PEREIRA, UEL; MARIA CRISTINA NEVES DE OLIVEIRA, CNPSO; ALEXANDRE LIMA NEPOMUCENO, CNPSO; FRANCISMAR CORREA MARCELINO, CNPSO. |
Título: |
Identification of reference genes for expression analysis by real-time quantitative PCR in drought-stressed soybean. |
Ano de publicação: |
2011 |
Fonte/Imprenta: |
Pesquisa Agropecuária Brasileira, Brasília, DF, v. 46, n. 1, p. 58-65, jan. 2011. |
Idioma: |
Inglês |
Conteúdo: |
The objective of this work was to validate, by quantitative PCR in real time (RT-qPCR), genes to be used as reference in studies of gene expression in soybean in drought-stressed trials. Four genes commonly used in soybean were evaluated: GmB-actin, GmGAPDH, GmLectin and GmRNAr18S. Total RNA was extracted from six samples: three from roots in a hydroponic system with different drought intensities (0, 25, 50, 75 and 100 minutes of water stress), and three from leaves of plants grown in sand with different soil moistures (15, 5 and 2.5% gravimetric humidity). The raw cycle threshold (Ct) data were analyzed, and the efficiency of each primer was calculated for an overall analysis of the Ct range among the different samples. The GeNorm application was used to evaluate the best reference gene, according to its stability. The GmGAPDH was the least stable gene, with the highest mean values of expression stability (M), and the most stable genes, with the lowest M values, were the GmB-actin and GmRNAr18S, when both root and leaves samples were tested. These genes can be used in RT-qPCR as reference gene for expression analysis. |
Palavras-Chave: |
Déficit hídrico; Estabilidade de expressão; Expressão gênica; Expression stability; RT-qPCR. |
Thesagro: |
Biotecnologia; Deficiência hídrica; Glycine Max; Soja. |
Thesaurus NAL: |
Agricultural biotechnology; Gene expression; Plant-water relations; Soybeans. |
Categoria do assunto: |
-- F Plantas e Produtos de Origem Vegetal |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/31023/1/46n01a08.pdf
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/168638/1/Identification-of-reference-genes-for-expression.pdf
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Marc: |
LEADER 02275naa a2200373 a 4500 001 1882641 005 2011-10-14 008 2011 bl uuuu u00u1 u #d 100 1 $aSTOLF-MOREIRA, R. 245 $aIdentification of reference genes for expression analysis by real-time quantitative PCR in drought-stressed soybean. 260 $c2011 520 $aThe objective of this work was to validate, by quantitative PCR in real time (RT-qPCR), genes to be used as reference in studies of gene expression in soybean in drought-stressed trials. Four genes commonly used in soybean were evaluated: GmB-actin, GmGAPDH, GmLectin and GmRNAr18S. Total RNA was extracted from six samples: three from roots in a hydroponic system with different drought intensities (0, 25, 50, 75 and 100 minutes of water stress), and three from leaves of plants grown in sand with different soil moistures (15, 5 and 2.5% gravimetric humidity). The raw cycle threshold (Ct) data were analyzed, and the efficiency of each primer was calculated for an overall analysis of the Ct range among the different samples. The GeNorm application was used to evaluate the best reference gene, according to its stability. The GmGAPDH was the least stable gene, with the highest mean values of expression stability (M), and the most stable genes, with the lowest M values, were the GmB-actin and GmRNAr18S, when both root and leaves samples were tested. These genes can be used in RT-qPCR as reference gene for expression analysis. 650 $aAgricultural biotechnology 650 $aGene expression 650 $aPlant-water relations 650 $aSoybeans 650 $aBiotecnologia 650 $aDeficiência hídrica 650 $aGlycine Max 650 $aSoja 653 $aDéficit hídrico 653 $aEstabilidade de expressão 653 $aExpressão gênica 653 $aExpression stability 653 $aRT-qPCR 700 1 $aLEMOS, E. G. de M. 700 1 $aABDELNOOR, R. V. 700 1 $aBENEVENTI, M. A. 700 1 $aROLLA, A. A. P. 700 1 $aPEREIRA, S. dos S. 700 1 $aOLIVEIRA, M. C. N. de 700 1 $aNEPOMUCENO, A. L. 700 1 $aMARCELINO-GUIMARÃES, F. C. 773 $tPesquisa Agropecuária Brasileira, Brasília, DF$gv. 46, n. 1, p. 58-65, jan. 2011.
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