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Both the control mice and the genetically modified group had "normal background levels of autophagy" during everyday circumstances, Dr. Levine points out.
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Only background levels of staining were observed (data not shown).
Background levels of genetic alterations.
Only background levels of 3-nitroTyr were detected with dONOO.
Background levels of empty clones were less than 10%.
This can be the background level of translational selection.
Protein levels of autophagy markers LC3B and p62 were decreased and increased, respectively.
Exposure to H2O2 upregulated the levels of autophagy marker LC3-II in a time-course manner (Fig. 3A).
Low levels of autophagy may also critically contribute to the selective survival and growth of UV-irradiated melanoma-cell escapers.
Levels of autophagy protein marker Atg5, and LC3B were decreased and level of p62 was elevated in hyperglycemic condition, the effects of which were reversed by ALHD2.
We determined if CD40 not only increased expression of autophagy protein but also enhanced basal levels of autophagy.
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