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  • Author or Editor: J. Kőmives x
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Changes in the water content of aluminium sulphate hydrate were investigated gravimetrically at room temperature in air with different relative humidities. The samples conditioned in this way were characterized by thermoanalytical (TG, DTG, DSC) and X-ray diffraction measurements. Industrial aluminium sulphate hydrate obtained by freezing the melt has a partly crystalline structure. After grinding, this material crystallizes during storage. This process requires a humid atmosphere; increasing relative humidity brings about more intensive crystallization.

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The gibbsite →χ-alumina decomposition (in air) and theχ-alumina → boehmite transformation (under hydrothermal conditions) were investigated isothermally. Reaction products were characterized by TG and X-ray diffraction.

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Thermogravimetry was applied in studies of aluminium foils for electrolytic capacitors. Scanning electron microscopy, X-ray diffraction and surface area determination were also used in the interpretation of the results.

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As DNA methylation patterns are inherited (‘epigenetic memory’) gsh I transgenic poplar ( Populus × canescens ) clones (11 ggs and 6 Lgl ) were treated with the DNA demethylating drug DHAC (5,6-dihydro-5′-azacytidine hydrochloride) at 10 −4 M for 7 days in order to study acquired plant molecular defense mechanisms in novel plant sources. In this study, the response of relative gene expression levels of transgene gsh I and poplar gene gsh 1 to DHAC treatment were analyzed by qRT-PCR ( q uantitative r everse t ranscriptase PCR). High expression levels of transgene gsh I were observed in the 6 Lgl clone (13.5-fold increase) compared to 11 ggs (1.0) sample. The expression level doubled (1.8-fold increase) in the DHAC-treated 6 Lgl samples but not in the 11 ggs clone (0.4-fold). Contrary to this, the relative copy number of transgene gsh I in the 6 Lgl clone was found to be 60% less (1.0) than in the 11 ggs sample (1.6). Relative expression level of endogenous poplar gene gsh 1 showed significantly higher responsiveness to DHAC-induced demethylation than the transgene gsh I with the highest expression level in the untransformed WT poplar (19.7-fold increase) compared to transformed clones of 6 Lgl (8.7-fold increase) and 11 ggs (2.5-fold increase), respectively. Competition in the reactivation capacity between transgene gsh I and poplar gsh 1 of 6 Lgl clone was also observed as the relative gene expression level of transgene gsh I increased from a high relative expression level (13.5) up by about twofold (1.8 times) rate (to 23.7) compared to poplar gsh 1 gene that increased by an 8.7 increment from a lower level (1.6 rel. expression) to 13.9.

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