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  • Fonte: Protein Expression and Purification. Unidade: FFCLRP

    Assuntos: NANOPARTÍCULAS, ASCOMYCOTA, CINÉTICA, ENZIMAS

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    • ABNT

      CARLI, Sibeli et al. Immobilization of a β-glucosidase and an endoglucanase in ferromagnetic nanoparticles: a study of synergistic effects. Protein Expression and Purification, v. 160, p. 28-35, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2019.03.016. Acesso em: 27 jun. 2024.
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      Carli, S., Carneiro, L. A. B. de C., Ward, R. J., & Meleiro, L. P. (2019). Immobilization of a β-glucosidase and an endoglucanase in ferromagnetic nanoparticles: a study of synergistic effects. Protein Expression and Purification, 160, 28-35. doi:10.1016/j.pep.2019.03.016
    • NLM

      Carli S, Carneiro LAB de C, Ward RJ, Meleiro LP. Immobilization of a β-glucosidase and an endoglucanase in ferromagnetic nanoparticles: a study of synergistic effects [Internet]. Protein Expression and Purification. 2019 ; 160 28-35.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2019.03.016
    • Vancouver

      Carli S, Carneiro LAB de C, Ward RJ, Meleiro LP. Immobilization of a β-glucosidase and an endoglucanase in ferromagnetic nanoparticles: a study of synergistic effects [Internet]. Protein Expression and Purification. 2019 ; 160 28-35.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2019.03.016
  • Fonte: Protein Expression and Purification. Unidade: IB

    Assuntos: ENZIMAS, SOLUBILIZAÇÃO, BACTÉRIAS PATOGÊNICAS, PROTEÍNAS, BIOLOGIA MOLECULAR, BIOQUÍMICA

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    • ABNT

      LEMKE, Laura Simoni et al. Investigation on solubilization protocols in the refolding of the thioredoxin TsnC from Xylella fastidiosa by high hydrostatic pressure approach. Protein Expression and Purification, v. 106, p. 72-77, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2014.10.013. Acesso em: 27 jun. 2024.
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      Lemke, L. S., Chura-Chambi, R. M., Rodrigues, D., Cussiol, J. R. R., Malavasi, N. V., Alegria, T. G. P., et al. (2015). Investigation on solubilization protocols in the refolding of the thioredoxin TsnC from Xylella fastidiosa by high hydrostatic pressure approach. Protein Expression and Purification, 106, 72-77. doi:10.1016/j.pep.2014.10.013
    • NLM

      Lemke LS, Chura-Chambi RM, Rodrigues D, Cussiol JRR, Malavasi NV, Alegria TGP, Netto LES, Morganti L. Investigation on solubilization protocols in the refolding of the thioredoxin TsnC from Xylella fastidiosa by high hydrostatic pressure approach [Internet]. Protein Expression and Purification. 2015 ; 106 72-77.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2014.10.013
    • Vancouver

      Lemke LS, Chura-Chambi RM, Rodrigues D, Cussiol JRR, Malavasi NV, Alegria TGP, Netto LES, Morganti L. Investigation on solubilization protocols in the refolding of the thioredoxin TsnC from Xylella fastidiosa by high hydrostatic pressure approach [Internet]. Protein Expression and Purification. 2015 ; 106 72-77.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2014.10.013
  • Fonte: Protein Expression and Purification. Unidade: IFSC

    Assuntos: CLONAGEM, ENZIMAS, PROTEÍNAS (CARACTERÍSTICAS)

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    • ABNT

      CAMILO, Cesar M. e POLIKARPOV, Igor. High-throughput cloning, expression and purification of glycoside hydrolases using Ligation-Independent Cloning (LIC). Protein Expression and Purification, v. 99, p. 35-42, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2014.03.008. Acesso em: 27 jun. 2024.
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      Camilo, C. M., & Polikarpov, I. (2014). High-throughput cloning, expression and purification of glycoside hydrolases using Ligation-Independent Cloning (LIC). Protein Expression and Purification, 99, 35-42. doi:10.1016/j.pep.2014.03.008
    • NLM

      Camilo CM, Polikarpov I. High-throughput cloning, expression and purification of glycoside hydrolases using Ligation-Independent Cloning (LIC) [Internet]. Protein Expression and Purification. 2014 ; 99 35-42.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2014.03.008
    • Vancouver

      Camilo CM, Polikarpov I. High-throughput cloning, expression and purification of glycoside hydrolases using Ligation-Independent Cloning (LIC) [Internet]. Protein Expression and Purification. 2014 ; 99 35-42.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2014.03.008
  • Fonte: Protein Expression and Purification. Unidade: IFSC

    Assuntos: RNA DE TRANSFERÊNCIA, FLUORESCÊNCIA, ENZIMAS

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    • ABNT

      MANZINE, Livia Regina et al. An efficient protocol for the production of tRNA-free recombinant Selenocysteine Synthase (SELA) from Escherichia coli and its biophysical characterization. Protein Expression and Purification, v. 88, n. 1, p. 80-84, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2012.12.005. Acesso em: 27 jun. 2024.
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      Manzine, L. R., Cassago, A., Silva, M. T. A. da, & Thiemann, O. H. (2013). An efficient protocol for the production of tRNA-free recombinant Selenocysteine Synthase (SELA) from Escherichia coli and its biophysical characterization. Protein Expression and Purification, 88( 1), 80-84. doi:10.1016/j.pep.2012.12.005
    • NLM

      Manzine LR, Cassago A, Silva MTA da, Thiemann OH. An efficient protocol for the production of tRNA-free recombinant Selenocysteine Synthase (SELA) from Escherichia coli and its biophysical characterization [Internet]. Protein Expression and Purification. 2013 ; 88( 1): 80-84.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2012.12.005
    • Vancouver

      Manzine LR, Cassago A, Silva MTA da, Thiemann OH. An efficient protocol for the production of tRNA-free recombinant Selenocysteine Synthase (SELA) from Escherichia coli and its biophysical characterization [Internet]. Protein Expression and Purification. 2013 ; 88( 1): 80-84.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2012.12.005
  • Fonte: Protein Expression and Purification. Unidades: FFCLRP, IQ

    Assuntos: ESCHERICHIA COLI, ENZIMAS

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    • ABNT

      ALMEIDA, Fabiana Maria de et al. Heterologous expression in Escherichia coli of Neurospora crassa neutral trehalase as an active enzyme. Protein Expression and Purification, v. 65, n. 2, p. 185-189, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2008.11.010. Acesso em: 27 jun. 2024.
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      Almeida, F. M. de, Bonini, B. M., Beton, D., Jorge, J. A., Terenzi, H. F., & Da Silva, A. M. (2009). Heterologous expression in Escherichia coli of Neurospora crassa neutral trehalase as an active enzyme. Protein Expression and Purification, 65( 2), 185-189. doi:10.1016/j.pep.2008.11.010
    • NLM

      Almeida FM de, Bonini BM, Beton D, Jorge JA, Terenzi HF, Da Silva AM. Heterologous expression in Escherichia coli of Neurospora crassa neutral trehalase as an active enzyme [Internet]. Protein Expression and Purification. 2009 ; 65( 2): 185-189.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2008.11.010
    • Vancouver

      Almeida FM de, Bonini BM, Beton D, Jorge JA, Terenzi HF, Da Silva AM. Heterologous expression in Escherichia coli of Neurospora crassa neutral trehalase as an active enzyme [Internet]. Protein Expression and Purification. 2009 ; 65( 2): 185-189.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2008.11.010
  • Fonte: Protein Expression and Purification. Unidades: IQSC, IFSC

    Assuntos: ENZIMAS, CLONAGEM, ESPECTROSCOPIA, FLUORESCÊNCIA, PROTEÍNAS, BACTÉRIAS FITOPATOGÊNICAS, FRUTAS CÍTRICAS

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    • ABNT

      TRAVENSOLO, Regiane de Fátima et al. Cloning, expression, purification and characterization of recombinant glutathione-S-transferase from Xylella fastidiosa. Protein Expression and Purification, v. 59, n. 1, p. 153-160, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2008.01.017. Acesso em: 27 jun. 2024.
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      Travensolo, R. de F., Garcia, W., Muniz, J. R. C., Caruso, C. S., Lemos, E. G. M., Carrilho, E., & Araújo, A. P. U. de. (2008). Cloning, expression, purification and characterization of recombinant glutathione-S-transferase from Xylella fastidiosa. Protein Expression and Purification, 59( 1), 153-160. doi:10.1016/j.pep.2008.01.017
    • NLM

      Travensolo R de F, Garcia W, Muniz JRC, Caruso CS, Lemos EGM, Carrilho E, Araújo APU de. Cloning, expression, purification and characterization of recombinant glutathione-S-transferase from Xylella fastidiosa [Internet]. Protein Expression and Purification. 2008 ; 59( 1): 153-160.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2008.01.017
    • Vancouver

      Travensolo R de F, Garcia W, Muniz JRC, Caruso CS, Lemos EGM, Carrilho E, Araújo APU de. Cloning, expression, purification and characterization of recombinant glutathione-S-transferase from Xylella fastidiosa [Internet]. Protein Expression and Purification. 2008 ; 59( 1): 153-160.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2008.01.017
  • Fonte: Protein Expression and Purification. Unidade: IFSC

    Assuntos: ENZIMAS, PROTEÍNAS

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    • ABNT

      REYES, Luis F. et al. Expression, purification, and structural analysis of HIS UBE2G2 (human ubiquitin-conjugating enzyme). Protein Expression and Purification, v. 45, n. 2, p. 324-328, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2005.08.018. Acesso em: 27 jun. 2024.
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      Reyes, L. F., Sommer, C. A., Beltramini, L. M., & Silva, F. H. (2006). Expression, purification, and structural analysis of HIS UBE2G2 (human ubiquitin-conjugating enzyme). Protein Expression and Purification, 45( 2), 324-328. doi:10.1016/j.pep.2005.08.018
    • NLM

      Reyes LF, Sommer CA, Beltramini LM, Silva FH. Expression, purification, and structural analysis of HIS UBE2G2 (human ubiquitin-conjugating enzyme) [Internet]. Protein Expression and Purification. 2006 ; 45( 2): 324-328.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2005.08.018
    • Vancouver

      Reyes LF, Sommer CA, Beltramini LM, Silva FH. Expression, purification, and structural analysis of HIS UBE2G2 (human ubiquitin-conjugating enzyme) [Internet]. Protein Expression and Purification. 2006 ; 45( 2): 324-328.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2005.08.018
  • Fonte: Protein Expression and Purification. Unidade: IFSC

    Assuntos: ENZIMAS, CRISTALOGRAFIA, PROTEÍNAS, GLÂNDULA TIREOIDE

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    • ABNT

      SANTOS, Maria A. M. et al. Expression, purification, and characterization of rat protein tyrosine phosphatas 'eta'atalytic domain. Protein Expression and Purification, v. 41, n. 1, p. 113-120, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2005.01.018. Acesso em: 27 jun. 2024.
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      Santos, M. A. M., Santos, S. M., Matozo, H. C., Portugal, R. V., Iuliano, R., Fusco, A., & Polikarpov, I. (2005). Expression, purification, and characterization of rat protein tyrosine phosphatas 'eta'atalytic domain. Protein Expression and Purification, 41( 1), 113-120. doi:10.1016/j.pep.2005.01.018
    • NLM

      Santos MAM, Santos SM, Matozo HC, Portugal RV, Iuliano R, Fusco A, Polikarpov I. Expression, purification, and characterization of rat protein tyrosine phosphatas 'eta'atalytic domain [Internet]. Protein Expression and Purification. 2005 ; 41( 1): 113-120.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2005.01.018
    • Vancouver

      Santos MAM, Santos SM, Matozo HC, Portugal RV, Iuliano R, Fusco A, Polikarpov I. Expression, purification, and characterization of rat protein tyrosine phosphatas 'eta'atalytic domain [Internet]. Protein Expression and Purification. 2005 ; 41( 1): 113-120.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2005.01.018
  • Fonte: Protein Expression and Purification. Unidade: IFSC

    Assuntos: ENZIMAS, BIOFÍSICA, CRISTALOGRAFIA, PROTEÍNAS

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    • ABNT

      PIERI, Celina de et al. Overexpression, purification, and biochemical characterization of GumC, an enzyme involved in the biosynthesis of exopolysaccharide by Xylella fastidiosa. Protein Expression and Purification, v. 34, n. 2, p. 223-228, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2003.11.003. Acesso em: 27 jun. 2024.
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      Pieri, C. de, Beltramini, L. M., Selistre-de-Araújo, H. S., Vettore, A. L., Silva, F. R. da, Arruda, P., et al. (2004). Overexpression, purification, and biochemical characterization of GumC, an enzyme involved in the biosynthesis of exopolysaccharide by Xylella fastidiosa. Protein Expression and Purification, 34( 2), 223-228. doi:10.1016/j.pep.2003.11.003
    • NLM

      Pieri C de, Beltramini LM, Selistre-de-Araújo HS, Vettore AL, Silva FR da, Arruda P, Oliva G, Souza DHF de. Overexpression, purification, and biochemical characterization of GumC, an enzyme involved in the biosynthesis of exopolysaccharide by Xylella fastidiosa [Internet]. Protein Expression and Purification. 2004 ; 34( 2): 223-228.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2003.11.003
    • Vancouver

      Pieri C de, Beltramini LM, Selistre-de-Araújo HS, Vettore AL, Silva FR da, Arruda P, Oliva G, Souza DHF de. Overexpression, purification, and biochemical characterization of GumC, an enzyme involved in the biosynthesis of exopolysaccharide by Xylella fastidiosa [Internet]. Protein Expression and Purification. 2004 ; 34( 2): 223-228.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2003.11.003
  • Fonte: Protein Expression and Purification. Unidade: IFSC

    Assuntos: ENZIMAS, CRISTALOGRAFIA, DNA

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      RAZZERA, Guilherme et al. Expression, purification, and initial structural characterization of rat orphan nuclear receptor NOR-1 LDB domain. Protein Expression and Purification, v. 37, n. 2, p. 443-449, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2004.06.024. Acesso em: 27 jun. 2024.
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      Razzera, G., Vernal, J., Portugal, R. V., Calgaro, M. R., Fernandez, P., Zakin, M. M., et al. (2004). Expression, purification, and initial structural characterization of rat orphan nuclear receptor NOR-1 LDB domain. Protein Expression and Purification, 37( 2), 443-449. doi:10.1016/j.pep.2004.06.024
    • NLM

      Razzera G, Vernal J, Portugal RV, Calgaro MR, Fernandez P, Zakin MM, Polikarpov I, Terenzi H. Expression, purification, and initial structural characterization of rat orphan nuclear receptor NOR-1 LDB domain [Internet]. Protein Expression and Purification. 2004 ; 37( 2): 443-449.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2004.06.024
    • Vancouver

      Razzera G, Vernal J, Portugal RV, Calgaro MR, Fernandez P, Zakin MM, Polikarpov I, Terenzi H. Expression, purification, and initial structural characterization of rat orphan nuclear receptor NOR-1 LDB domain [Internet]. Protein Expression and Purification. 2004 ; 37( 2): 443-449.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.pep.2004.06.024
  • Fonte: Protein Expression and Purification. Unidades: FFCLRP, FMRP

    Assuntos: QUÍMICA, PROTEÍNAS, ENZIMAS

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    • ABNT

      WARD, Richard John et al. Refolding and purification of Bothropstoxin-I, a Lys49-phospholipase 'A IND.2' homologue, expressed as inclusion bodies in Escherichia coli. Protein Expression and Purification, v. 21, p. 134-140, 2001Tradução . . Disponível em: http://www.idealibrary.com/links/doi/10.1006/prep.2000.1353/pdf. Acesso em: 27 jun. 2024.
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      Ward, R. J., Oliveira, A. H. C. de, Bortoleto, R. K., Rosa, J. C., Faça, V. M., & Greene, L. J. (2001). Refolding and purification of Bothropstoxin-I, a Lys49-phospholipase 'A IND.2' homologue, expressed as inclusion bodies in Escherichia coli. Protein Expression and Purification, 21, 134-140. Recuperado de http://www.idealibrary.com/links/doi/10.1006/prep.2000.1353/pdf
    • NLM

      Ward RJ, Oliveira AHC de, Bortoleto RK, Rosa JC, Faça VM, Greene LJ. Refolding and purification of Bothropstoxin-I, a Lys49-phospholipase 'A IND.2' homologue, expressed as inclusion bodies in Escherichia coli [Internet]. Protein Expression and Purification. 2001 ; 21 134-140.[citado 2024 jun. 27 ] Available from: http://www.idealibrary.com/links/doi/10.1006/prep.2000.1353/pdf
    • Vancouver

      Ward RJ, Oliveira AHC de, Bortoleto RK, Rosa JC, Faça VM, Greene LJ. Refolding and purification of Bothropstoxin-I, a Lys49-phospholipase 'A IND.2' homologue, expressed as inclusion bodies in Escherichia coli [Internet]. Protein Expression and Purification. 2001 ; 21 134-140.[citado 2024 jun. 27 ] Available from: http://www.idealibrary.com/links/doi/10.1006/prep.2000.1353/pdf

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