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Pesquisa : E05.599.495 [Categoria DeCS]
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[PMID]:29431326
[Au] Autor:Khripach LV; Zheleznyak EV; Knyazeva TD; Koganova ZI; Salikhova DI; Grishin DA
[Ti] Título:[Method of colored model radicals for assessment of oxidative equilibrium in biologic samples].
[So] Source:Gig Sanit;95(9):884-90, 2016.
[Is] ISSN:0016-9900
[Cp] País de publicação:Russia (Federation)
[La] Idioma:rus
[Ab] Resumo:The most specific method of the recording of the rate offree radical reactions is the method of electron paramagnetic resonance (EPR) spectroscopy, but it is rarely used in applied biology due to expensive equipment and complexity of the execution of measurements. However chemists have found a number of colored organic radicals which lose the coloring under transition into diamagnetic form. In the given paper there are presented results of our studies on the development of methods for the assessment of oxidant equilibrium in biological media with a use of stable radical 2,2-diphenyl-1-picrylhydrazyl (DPPH) and cation-radicals of N,N-diethyl-p-phenylenediamine (DEPPD). We have developed the new modification of DPPH test, replacing methanol-based incubation medium by non-ionic detergent solution, compatible with native blood serum. Modified DPPH test conserved typical biphasic kinetics of the origin variant, had the similar sensitivity to model antioxidants (IC values 49, 38 and 13 mkMfor ascorbate, a-tocopherol and quercetine, correspondingly) and was applied in experiments on laboratory animals treated with nano- and ionic silver, carbon nanotubes, microfine coal and electrolytic dust. We have tried also the assay of serum lipid hydroperoxides based on Fe-initiated DEPPD oxidation (Alberti et al., 2000). The comparison of kinetics of DEPPD oxidation in model (HO/Fe) and biologic (rat serum/Fe) systems, before and after Fe addition, seems to be an evidence that ceruloplasmin (CP) was involved in the resulting process, but failed to determine its polynomial kinetics, at least for the rat serum and DEPPD excess. The use of CP monoclonal antibodies seems to be the best way for the clarification of the mechanism of this reaction.
[Mh] Termos MeSH primário: Compostos de Bifenilo
Oxirredução
Fenilenodiaminas
Picratos
Plasma
[Mh] Termos MeSH secundário: Animais
Fenômenos Bioquímicos
Compostos de Bifenilo/análise
Compostos de Bifenilo/química
Compostos de Bifenilo/metabolismo
Corantes/análise
Corantes/química
Indicadores e Reagentes/análise
Indicadores e Reagentes/química
Modelos Químicos
Fenilenodiaminas/análise
Fenilenodiaminas/química
Fenilenodiaminas/metabolismo
Picratos/análise
Picratos/química
Picratos/metabolismo
Plasma/química
Plasma/metabolismo
Ratos
Kit de Reagentes para Diagnóstico
Reprodutibilidade dos Testes
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Biphenyl Compounds); 0 (Coloring Agents); 0 (Indicators and Reagents); 0 (Phenylenediamines); 0 (Picrates); 0 (Reagent Kits, Diagnostic); 93-05-0 (N,N-diethyl 4-phenylenediamine); DFD3H4VGDH (1,1-diphenyl-2-picrylhydrazyl)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180309
[Lr] Data última revisão:
180309
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180213
[St] Status:MEDLINE


  2 / 83803 MEDLINE  
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[PMID]:29286779
[Au] Autor:Chuang HM; Reifenberger JG; Cao H; Dorfman KD
[Ad] Endereço:Department of Chemical Engineering and Materials Science, University of Minnesota-Twin Cities, 421 Washington Avenue SE, Minneapolis, Minnesota 55455, USA.
[Ti] Título:Sequence-Dependent Persistence Length of Long DNA.
[So] Source:Phys Rev Lett;119(22):227802, 2017 Dec 01.
[Is] ISSN:1079-7114
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Using a high-throughput genome-mapping approach, we obtained circa 50 million measurements of the extension of internal human DNA segments in a 41 nm×41 nm nanochannel. The underlying DNA sequences, obtained by mapping to the reference human genome, are 2.5-393 kilobase pairs long and contain percent GC contents between 32.5% and 60%. Using Odijk's theory for a channel-confined wormlike chain, these data reveal that the DNA persistence length increases by almost 20% as the percent GC content increases. The increased persistence length is rationalized by a model, containing no adjustable parameters, that treats the DNA as a statistical terpolymer with a sequence-dependent intrinsic persistence length and a sequence-independent electrostatic persistence length.
[Mh] Termos MeSH primário: DNA/química
DNA/genética
Modelos Químicos
Modelos Genéticos
[Mh] Termos MeSH secundário: Sequência de Bases
Sequenciamento de Nucleotídeos em Larga Escala/métodos
Seres Humanos
Relação Estrutura-Atividade
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
9007-49-2 (DNA)
[Em] Mês de entrada:1801
[Cu] Atualização por classe:180309
[Lr] Data última revisão:
180309
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171230
[St] Status:MEDLINE
[do] DOI:10.1103/PhysRevLett.119.227802


  3 / 83803 MEDLINE  
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[PMID]:28867554
[Au] Autor:Zhu LJ; Zhao Y; Chen YN; Cui HY; Wei YQ; Liu HL; Chen XM; Wei ZM
[Ad] Endereço:College of Life Science, Northeast Agricultural University, Harbin 150030, China.
[Ti] Título:Characterization of atrazine binding to dissolved organic matter of soil under different types of land use.
[So] Source:Ecotoxicol Environ Saf;147:1065-1072, 2018 Jan.
[Is] ISSN:1090-2414
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Atrazine is widely used in agriculture. In this study, dissolved organic matter (DOM) from soils under four types of land use (forest (F), meadow (M), cropland (C) and wetland (W)) was used to investigate the binding characteristics of atrazine. Fluorescence excitation-emission matrix-parallel factor (EEM-PARAFAC) analysis, two-dimensional correlation spectroscopy (2D-COS) and Stern-Volmer model were combined to explore the complexation between DOM and atrazine. The EEM-PARAFAC indicated that DOM from different sources had different structures, and humic-like components had more obvious quenching effects than protein-like components. The Stern-Volmer model combined with correlation analysis showed that log K values of PARAFAC components had a significant correlation with the humification of DOM, especially for C3 component, and they were all in the same order as follows: meadow soil (5.68)>wetland soil (5.44)>cropland soil (5.35)>forest soil (5.04). The 2D-COS further confirmed that humic-like components firstly combined with atrazine followed by protein-like components. These findings suggest that DOM components can significantly influence the bioavailability, mobility and migration of atrazine in different land uses.
[Mh] Termos MeSH primário: Atrazina/análise
Substâncias Húmicas/análise
Modelos Químicos
Poluentes do Solo/análise
Solo/química
[Mh] Termos MeSH secundário: Agricultura
Atrazina/química
Florestas
Poluentes do Solo/química
Espectrometria de Fluorescência/métodos
Zonas Úmidas
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Humic Substances); 0 (Soil); 0 (Soil Pollutants); QJA9M5H4IM (Atrazine)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180308
[Lr] Data última revisão:
180308
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170905
[St] Status:MEDLINE


  4 / 83803 MEDLINE  
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[PMID]:28278779
[Au] Autor:Lominchar MA; Rodríguez S; Lorenzo D; Santos N; Romero A; Santos A
[Ad] Endereço:a Dpto. Ingeniería Química, Facultad CC, Químicas , Universidad Complutense de Madrid , Madrid , Spain.
[Ti] Título:Phenol abatement using persulfate activated by nZVI, H O and NaOH and development of a kinetic model for alkaline activation.
[So] Source:Environ Technol;39(1):35-43, 2018 Jan.
[Is] ISSN:0959-3330
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Three persulfate (PS) activation methods (nanoparticles of zero-valent iron (nZVI), hydrogen peroxide and alkali) were compared using phenol as target pollutant. Firstly, four experiments were conducted at 25°C in a batch way using the same initial phenol and oxidant concentrations (10 mM and 420 mM, respectively), being the molar ratio activator/PS fixed to 0.005 with nZVI (mass ratio 0.0011 nZVI/PS), to 2 using hydrogen peroxide and to 2 and 4 with NaOH. Phenol and PS conversions and aromatic byproducts profiles during 168 h reaction time were measured and compared, as well as mineralization and ecotoxicity of the samples. It was found that both phenol and aromatic byproducts (catechol and hydroquinone) totally disappeared using PS activated by alkali before 24 h, while a significant amount of aromatic intermediates was obtained with nZVI and H O . Additional runs were carried out using shorter times (0-2 h) to discriminate the oxidation route and the kinetic model of phenol abatement by using PS activated by alkali. Different initial concentrations of phenol (5-15 mM), PS (210 and 420 mM) and molar ratio NaOH/PS (2 and 4) were employed. The kinetic model obtained predicts accurately the evolution of phenol, persulfate, hydroquinone and catechol.
[Mh] Termos MeSH primário: Modelos Químicos
Nanopartículas/química
Fenol/química
Hidróxido de Sódio/química
Sulfatos/química
Poluentes Químicos da Água/química
[Mh] Termos MeSH secundário: Peróxido de Hidrogênio
Ferro
Cinética
Oxirredução
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Sulfates); 0 (Water Pollutants, Chemical); 339NCG44TV (Phenol); 55X04QC32I (Sodium Hydroxide); BBX060AN9V (Hydrogen Peroxide); E1UOL152H7 (Iron)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180308
[Lr] Data última revisão:
180308
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170311
[St] Status:MEDLINE
[do] DOI:10.1080/09593330.2017.1294203


  5 / 83803 MEDLINE  
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[PMID]:28278773
[Au] Autor:Feng Y; Liao C; Li H; Liu C; Shih K
[Ad] Endereço:a Department of Civil Engineering , The University of Hong Kong , Hong Kong.
[Ti] Título:Cu O-promoted degradation of sulfamethoxazole by α-Fe O -catalyzed peroxymonosulfate under circumneutral conditions: synergistic effect, Cu/Fe ratios, and mechanisms.
[So] Source:Environ Technol;39(1):1-11, 2018 Jan.
[Is] ISSN:0959-3330
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:To promote the application of iron oxides in sulfate radical-based advanced oxidation processes, a convenient approach using Cu O as a catalyst additive was proposed. Composite catalysts based on α-Fe O (CTX%Cu O, X = 1, 2.5, 5, and 10) were prepared for peroxymonosulfate (PMS) activation, and sulfamethoxazole was used as a model pollutant to probe the catalytic reactivity. The results show that a synergistic catalytic effect exists between Cu O and α-Fe O , which was explained by the promoted reduction of Fe(III) by Cu(I). Iron K-edge X-ray absorption spectroscopy investigations indicated that the promoted reduction probably occurred with PMS acting as a ligand that bridges the redox centers of Cu(I) and Fe(III). The weight ratio between Cu O and α-Fe O influenced the degradation of sulfamethoxazole, and the optimal ratio depended on the dosage of PMS and catalysts. With 40 mg L PMS and 0.6 g L catalyst, a pseudo-first-order constant of ∼0.019 min was achieved for CT2.5%Cu O, whereas only 0.004 min was realized for α-Fe O . Nearly complete degradation of the sulfamethoxazole was achieved within 180 min under the conditions of 40 mg L PMS, 0.4 g L CT2.5%Cu O, and pH 6.8. In contrast, less than 20% degradation was realized with α-Fe O under similar conditions. The CT2.5%Cu O catalyst had the best stoichiometric efficiency of PMS (0.317), which was 4.5 and 5.8 times higher than those of Cu O (0.070) and α-Fe O (0.054), respectively. On the basis of the products identified, the cleavage of the S-N bond was proposed as a major pathway for the degradation of sulfamethoxazole.
[Mh] Termos MeSH primário: Modelos Químicos
Sulfametoxazol/química
Poluentes Químicos da Água/química
[Mh] Termos MeSH secundário: Cobre/química
Compostos Férricos/química
Ferro/química
Peróxidos/química
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Ferric Compounds); 0 (Peroxides); 0 (Water Pollutants, Chemical); 1K09F3G675 (ferric oxide); 22047-43-4 (peroxymonosulfate); 789U1901C5 (Copper); E1UOL152H7 (Iron); JE42381TNV (Sulfamethoxazole)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180308
[Lr] Data última revisão:
180308
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170311
[St] Status:MEDLINE
[do] DOI:10.1080/09593330.2017.1293164


  6 / 83803 MEDLINE  
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[PMID]:28264625
[Au] Autor:Zhao C; Wang CC; Li JQ; Wang P; Ou JQ; Cui JR
[Ad] Endereço:a Beijing Key Laboratory of Functional Materials for Building Structure and Environment , Remediation Beijing University of Civil Engineering and Architecture , Beijing , People's Republic of China.
[Ti] Título:Interactions between copper(II) and DOM in the urban stormwater runoff: modeling and characterizations.
[So] Source:Environ Technol;39(1):120-129, 2018 Jan.
[Is] ISSN:0959-3330
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Dissolved organic matter (DOM) can strongly interact with both organic and inorganic contaminants to influence their transportation, transformation, bioavailability, toxicity and even their ultimate fate. Within this work, DOM was extracted from urban stormwater runoff samples collected from a regular sampling site of a typical residential area in Beijing, China. Copper(II) ions were selected as model to investigate the interactions between DOM and typical heavy metals. Both ultraviolet (UV) absorbance and fluorescence titration methods were introduced to determine the complex capacities (C ) and conditional stability constants (log K ) of bonding between DOM and copper (II) ions, which revealed that the values of C were 85.62 and 87.23 µmol mg and the log K values were 5.37 and 5.48, respectively. The results suggested the successful complexation between DOM and copper(II) ions. Furthermore, morphology of the DOM binding to copper(II) ions was confirmed by both energy-dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS), which can facilitate to clarify the corresponding mechanism. The Cu 2p peak at 933.7 eV and the characteristic shake-up peaks of Cu-O were found in the XPS spectra, implying that copper(II) ions might coordinate with hydroxyl (aliphatic or phenolic) or carboxyl groups. With these profitable results, it can be concluded that DOM in urban stormwater runoff has a strong binding affinity with copper(II) ions, which may further lead to potentially significant influence on their migration and transformation.
[Mh] Termos MeSH primário: Cobre/química
Modelos Químicos
Chuvas
Poluentes Químicos da Água/química
[Mh] Termos MeSH secundário: Pequim
Substâncias Húmicas/análise
Águas Residuais/química
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Humic Substances); 0 (Waste Water); 0 (Water Pollutants, Chemical); 789U1901C5 (Copper)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180308
[Lr] Data última revisão:
180308
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170308
[St] Status:MEDLINE
[do] DOI:10.1080/09593330.2017.1296893


  7 / 83803 MEDLINE  
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[PMID]:29335413
[Au] Autor:Abberley JP; Killah R; Walker R; Storey JMD; Imrie CT; Salamonczyk M; Zhu C; Gorecka E; Pociecha D
[Ad] Endereço:Department of Chemistry, King's College, University of Aberdeen, Aberdeen, AB24 3UE, UK.
[Ti] Título:Heliconical smectic phases formed by achiral molecules.
[So] Source:Nat Commun;9(1):228, 2018 01 15.
[Is] ISSN:2041-1723
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Chiral symmetry breaking in soft matter is a hot topic of current research. Recently, such a phenomenon was found in a fluidic phase showing orientational order of molecules-the nematic phase; although built of achiral molecules, the phase can exhibit structural chirality-average molecular direction follows a short-pitch helix. Here, we report a series of achiral asymmetric dimers with an odd number of atoms in the spacer, which form twisted structures in nematic as well as in lamellar phases. The tight pitch heliconical nematic (N ) phase and heliconical tilted smectic C (SmC ) phase are formed. The formation of a variety of helical structures is accompanied by a gradual freezing of molecular rotation. In the lowest temperature smectic phase, HexI, the twist is expressed through the formation of hierarchical structure: nanoscale helices and mesoscopic helical filaments. The short-pitch helical structure in the smectic phases is confirmed by resonant X-ray measurements.
[Mh] Termos MeSH primário: Cristais Líquidos/química
Conformação Molecular
Nanoestruturas/química
Transição de Fase
[Mh] Termos MeSH secundário: Dicroísmo Circular
Isomerismo
Microscopia de Força Atômica
Modelos Químicos
Modelos Moleculares
Estrutura Molecular
Difração de Raios X
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180305
[Lr] Data última revisão:
180305
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180117
[St] Status:MEDLINE
[do] DOI:10.1038/s41467-017-02626-6


  8 / 83803 MEDLINE  
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[PMID]:29323115
[Au] Autor:Becker S; Schneider C; Okamura H; Crisp A; Amatov T; Dejmek M; Carell T
[Ad] Endereço:Center for Integrated Protein Science Munich CiPSM at the Department of Chemistry, Ludwig-Maximilians-Universität München, 81377, Munich, Germany.
[Ti] Título:Wet-dry cycles enable the parallel origin of canonical and non-canonical nucleosides by continuous synthesis.
[So] Source:Nat Commun;9(1):163, 2018 01 11.
[Is] ISSN:2041-1723
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:The molecules of life were created by a continuous physicochemical process on an early Earth. In this hadean environment, chemical transformations were driven by fluctuations of the naturally given physical parameters established for example by wet-dry cycles. These conditions might have allowed for the formation of (self)-replicating RNA as the fundamental biopolymer during chemical evolution. The question of how a complex multistep chemical synthesis of RNA building blocks was possible in such an environment remains unanswered. Here we report that geothermal fields could provide the right setup for establishing wet-dry cycles that allow for the synthesis of RNA nucleosides by continuous synthesis. Our model provides both the canonical and many ubiquitous non-canonical purine nucleosides in parallel by simple changes of physical parameters such as temperature, pH and concentration. The data show that modified nucleosides were potentially formed as competitor molecules. They could in this sense be considered as molecular fossils.
[Mh] Termos MeSH primário: Biopolímeros/química
Nucleosídeos/química
RNA/química
Água/química
[Mh] Termos MeSH secundário: Terra (Planeta)
Evolução Química
Modelos Químicos
Estrutura Molecular
Origem da Vida
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Biopolymers); 0 (Nucleosides); 059QF0KO0R (Water); 63231-63-0 (RNA)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180305
[Lr] Data última revisão:
180305
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180112
[St] Status:MEDLINE
[do] DOI:10.1038/s41467-017-02639-1


  9 / 83803 MEDLINE  
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[PMID]:29475280
[Au] Autor:Yuan R; Ye WJ; Xing HY; Li ZJ; Sun TT; Sun YB; Zhu JL; Xiang Y; Zhang ZY; Cai ML
[Ti] Título:Continuously adjustable period optical grating based on flexoelectric effect of a bent-core nematic liquid crystal in planar cells.
[So] Source:Opt Express;26(4):4288-4299, 2018 Feb 19.
[Is] ISSN:1094-4087
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The structures of flexodomains, which are similar to optical gratings and can be controlled by the amplitude of applied voltage and temperature, were verified through polarizing microscopy and light diffraction techniques. The properties of the optical grating induced by a bent-core nematic liquid crystal in planar cells with varied cell gaps and pretilt angles were studied. The period of optical grating decreases with the increase in the amplitude of the applied voltage and pretilt angle. In addition, the period increases with the increase in cell gap and temperature. The period of optical grating has a linear relationship with temperature. The continuously adjustable period has the potential to become an important and extended application of optical grating.
[Mh] Termos MeSH primário: Cristais Líquidos/química
Modelos Químicos
Modelos Moleculares
Óptica e Fotônica
[Mh] Termos MeSH secundário: Simulação por Computador
Módulo de Elasticidade
Campos Eletromagnéticos
Teste de Materiais
Refratometria/métodos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180302
[Lr] Data última revisão:
180302
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180225
[St] Status:MEDLINE
[do] DOI:10.1364/OE.26.004288


  10 / 83803 MEDLINE  
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[PMID]:29241086
[Au] Autor:Hameed R; Huddleston J; Ignatova S
[Ad] Endereço:Advanced Bioprocessing Centre, Institute of Environment, Health and Societies, College of Engineering, Design and Physical Sciences, Brunel University London, Uxbridge, UB8 3PH, UK.
[Ti] Título:Practical aspects of the automated preparation of aqueous two phase systems for the analysis of biological macromolecules.
[So] Source:J Chromatogr B Analyt Technol Biomed Life Sci;1073:60-68, 2018 Jan 15.
[Is] ISSN:1873-376X
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:A robust strategy for the automated preparation of aqueous two-phase systems (ATPS) using a liquid handling sample processor was developed using gravimetric methods: to determine the accuracy of preparation. The major robotic control parameters requiring adjustment were; speed of aspiration and dispense; delay times following aspiration and dispense alongside measures to control cross-contamination during phase sampling. In general mixture compositions of both polymer/polymer and polymer/salt mixtures could be prepared with a target bias accuracy of less than 5%. However, we found that the bias accuracy with which systems of defined TLL and MR could be constructed was highly dependent on the tie line length of the ATPS and the geometrical form of the ATPS co-existence curve. For systems with a very low degree of curvature (PEG/salt systems here) increases in bias (accuracy) are appreciable at relatively long tie line lengths. Where the degree of curvature is more pronounced (PEG/dextran systems) closer approach to the critical point was possible without major effect on bias/accuracy. Application of the strategy to the measurement of the partitioning of phosphorylated and dephosphorylated forms of the model protein ovalbumin are reported. Differences in partition of phosphorylated (native) forms and dephosphorylated forms could be demonstrated. In a PEG/salt system this was manifest as a substantial decrease in solubility based on overall protein recovery derived from accurate knowledge of the system mass ratio. In a PEG/dextran system differences in partition coefficient could be demonstrated between phosphorylated and dephosphorylated forms.
[Mh] Termos MeSH primário: Automação Laboratorial/métodos
Cromatografia Líquida/métodos
Extração Líquido-Líquido/métodos
Modelos Químicos
[Mh] Termos MeSH secundário: Ovalbumina/análise
Ovalbumina/química
Ovalbumina/isolamento & purificação
Isoformas de Proteínas/análise
Isoformas de Proteínas/química
Isoformas de Proteínas/isolamento & purificação
Proteínas Recombinantes/análise
Proteínas Recombinantes/química
Proteínas Recombinantes/isolamento & purificação
Robótica
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Protein Isoforms); 0 (Recombinant Proteins); 9006-59-1 (Ovalbumin)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180302
[Lr] Data última revisão:
180302
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171215
[St] Status:MEDLINE



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