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Co and Rh containing samples were proved to be stable catalysts, the impregnated Ni catalyst only slightly, while sol gel Ni samples slowly deactivated during the long term overnight run.
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The samples were proven to be non-toxic to tenocytes.
The samples were proven to have a potential use in photocatalyst, but suffered from photodissolution and memory effect.
All of the transformation events were confirmed by PCR, and representative samples were proven transgenic by Southern blotting.
The hydrogen peroxide scavenging activities of in vivo grown samples were proven to be more effective (P < 0.05) than the in vitro grown and callus samples, as revealed by the comparison with the EC50 values.
All analyzed tissue samples were proven to be of high molecular quality, and thorough histopathological evaluation to characterize the composition of the relative amounts of cancer and normal tissue was performed.
The RNA quality and quantity of all samples were proven using the Agilent 2100 Bioanalyzer and the RNA 6000 Nano Kits (Agilent, Waldbronn, Germany) and the Nanodrop 1000 Spectrophotometer (Thermo Scientific, MA, USA).
The presence of grafted protein on modified samples was proved using mass spectrometry.
The samples are proving tricky to get.
In the present study, an indirect competitive ELISA for the structure specific detection of cyathane type diterpenoids using polyclonal antibodies was developed, and its potential for the analysis of biological samples was proven.
In comparison to host guest polymer composite systems, long lifetime and high stability of the photorefractive sample was proved.
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