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Low sensor temperature to measure H2 is explained by a higher activity of H2 compared with CH4 and CO activities in oxidation reaction on the sensor surface.
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The study addresses a fundamental understanding of the effects of reaction conditions (syngas pressure, temperature and GHSV) and Re promotion on the Co activity and selectivity by SSITKA.
In Arabidopsis, 14-3-3 proteins alsoalso implicated in the regulation of CO activity [80].
CO activity is proposed to be restricted to LDs by an external coincidence model in which circadian clock control and light signalling combine to trigger CO activity (Searle and Coupland, 2004; Imaizumi and Kay, 2006).
The mechanism by which CO activity is controlled by day length involves both transcriptional and post-translational regulation.
Therefore, if COP1 exerts an effect to repress CO activity this should be reflected in reduced FT mRNA levels.
Two conserved cysteine and histidine amino acids in the Zn finger domain are essential for CO activity [ 6].
The expression of FT mRNA in cop1 4 mutants requires CO activity, as demonstrated by the absence of FT mRNA in cop1 4 co-10 plants.
The genetic and molecular experiments described earlier supported the hypothesis that COP1 negatively regulates CO activity at the post-transcriptional level.
Rather, PARP1's transcriptional co-activator activity is modified [ 150, 151].
However, while providing important information on gray matter activation, no information is gathered on the co-activity along white matter tracts in neural networks.
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