Isotopic Labelling
Mostrando 1-11 de 11 artigos, teses e dissertações.
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1. Geração de ozônio isotopicamente marcado com átomo de oxigênio-18, (18O3), formando oxigênio-18 molecular singlete, 18O2 (1Δg), e modificações na 2\ - desoxiguanosina / Isotopically labeled ozone, 18O3, generate 18O-labeled singlet molecular oxygen, 18O2 (1Δg), and oxidation of product of the purine moiety of 2\ -deoxyguanosine.
O ozônio (O3) é um poderoso oxidante e quantidades significativas podem ser formadas em ambientes urbanos, como resultado de uma série de eventos fotoquímicos, sendo um risco para a saúde humana. Devido a sua reatividade química, o ozônio é capaz de promover modificações oxidativas em diversas biomoléculas, tais como, DNA, proteínas e lipídios.
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 28/07/2011
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2. Oxidação do triptofano pelo oxigênio molecular no estado singlete [O2 (1Δg)]: estudos mecanísticos envolvendo marcação isotópica, espectrometria de massa e quimiluminescência / Tryptophan oxidation by singlet molecular oxygen [(O2(1Δg): mechanistic studies using isotopic labelling, mass spectrometry analysis and chemiluminescence
As proteínas são consideradas importantes alvos para os oxidantes, devido à abundância em sistemas biológicos e às altas constantes de reações com estas espécies. Adicionalmente, têmse demonstrado que o triptofano (W) é um aminoácido extremamente susceptível a oxidação, inclusive pelo oxigênio singlete (1O2). A reação do W com o 1O2 tem des
Publicado em: 2008
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3. Lipid hydroperoxides as a biological source of singlet oxygen: studies using isotopic labelling, mass spectrometry and luminescence / Hidroperóxidos de lipídios como fonte biológica de oxigênio singlete: estudos com marcação isotópica, espectrometria de massas e luminescência
Evidences point to the involvement of lipid peroxidation in several diseases. Lipid hydroperoxides (LOOH) are the primary products of lipid peroxidation and their decomposition generates more reactive and toxic compounds, such as peroxyl radicals. These radicals play an important role in the propagation of lipid peroxidation and may also generate singlet mol
Publicado em: 2005
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4. Aplicação da espectroscopia de ressonância magnética nuclear para estudos de difusão molecular em líquidos: a técnica DOSY
Diffusion coefficients provide uniquely detailed and easily interpreted information on molecular organization and phase structure. They are quite sensitive to structural changes, and to binding and association phenomena, in particular for liquid colloidal or macromolecular systems. This paper describes the principles of diffusion measurements in liquids by p
Química Nova. Publicado em: 2002-11
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5. Distribution of the marking with nitrogen 15 of protéicas fractions of beans-common (PHASEOLUS VULGARIS, L.) e isotópica dilution in the digestibilidade process in vitro. / Distribuição da marcação com nitrogenio 15 de frações proteicas de feijão-comum (Phaseolus vulgars L.) e diluição isotopica no processo de digestibilidade in vitro.
The aim of the present work was to verify if the isotope labelling with nitrogen 15 (15N) obtained in whole lyophilized beans, which had been labelled isotopically with 1.385% of 15N atoms of the total, was the same in the protein and protein fractions extracted from the beans. The aim was also to verify isotopic dilution of 15N, which occurs during in vitro
Publicado em: 1998
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6. A comparative study of digoxigenin, 2,4-dinitrophenyl, and alkaline phosphatase as deoxyoligonucleotide labels in non-radioisotopic in situ hybridisation.
AIM: To determine the optimum form of labelling and the most efficient reporter molecule for non-radioisotopic in situ hybridisation (ISH). METHODS: Nine deoxyoligonucleotides complementary to histone mRNA were synthesised and labelled either enzymatically or during solid-phase synthesis with the reporter molecules digoxigenin, 2,4-dinitrophenyl (DNP), or al
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7. Modification degrees at specific sites on heparan sulphate: an approach to measure chemical modifications on biological molecules with stable isotope labelling
Chemical modification of biological molecules is a general mechanism for cellular regulation. A quantitative approach has been developed to measure the extent of modification on HS (heparan sulphates). Sulphation on HS by sulphotransferases leads to variable sulphation levels, which allows cells to tune their affinities to various extracellular proteins, inc
Portland Press Ltd..
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8. Detection of specific DNA sequences using antibodies recognizing UV-labelled DNA.
This non-isotopic method for detection of nucleic acids is based on the in situ labelling of the nucleic acid by exposure to UV-irradiation. The different UV-induced photoproducts, mainly of the thymidine dimer type, are recognized by purified rabbit antibodies specific to the lesions introduced. The UV-labelled nucleic acids can then be visualized by conven
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9. A general protocol for evaluating the specific effects of DNA replication inhibitors.
Inhibitors of DNA replication in mammalian cells are of great interest because of their potential use in chemotherapy and in cell synchronizing protocols in the laboratory. We have used a combination of isotopic labelling protocols and a two-dimensional gel replicon mapping procedure to determine the specific effects of five different replication inhibitors
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10. Numerical chromosomal aberrations in Hodgkin's disease detected by in situ hybridisation on routine paraffin sections.
AIMS: To visualise directly numerical chromosomal aberrations and polyploidy in both Hodgkin and Reed Sternberg (HRS) cells and background cells from cases of Hodgkin's disease using in situ hybridisation. METHODS: Non-isotopic DNA in situ hybridisation was applied to interphase cell nuclei of Hodgkin's disease within routine paraffin embedded tissue section
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11. Non-isotopic in situ hybridisation and immunophenotyping of infected cells in the investigation of human fetal parvovirus infection.
AIMS: To compare the use of biotinylated and digoxigenin labelled probes for diagnosis of human fetal parvovirus B19 infection in formalin fixed, paraffin wax embedded tissues; and to assess the cellular distribution of the virus in positive cases. METHODS: Sections of lung tissue from 23 cases of anatomically normal non-immune fetal hydrops presenting betwe