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Murine heart tissue protein was extracted according to the manufacturer's instructions.
The let-7 family has been shown to be one of the most abundant miRNAs in murine heart tissue [ 46].
Other studies have shown that circadian clock genes in murine heart tissue are regulated differently under fasting and feeding conditions (22, 23).
These results were validated in vivo in a xenograft mouse model, as well as in murine heart tissue known to constitutively express B7-H1.
As shown in Figure 2, SIRT6 protein expression was detected in murine heart tissue isolated from the young, aged, and aged with ICA intervention groups.
Beyond this, hybrid variants of immunoproteasomes with constitutive subunits also have been identified in murine heart tissue as well as in human liver, colon, small intestine, kidneys, tumor cells and DCs [ 9].
Local NO levels in murine heart tissue were detected by spin trapping with iron dithiocarbamate complexes which is one of the most specific methods for NO detection in biological tissue.
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ICA can upregulate SIRT6 protein expression and downregulate NF- κB (p65) protein expression in murine heart tissues and in an aortic EC model.
In order to determine the best markers to isolate murine cardiac endothelial cells by flow cytometry, we first study the expression of several endothelial and other cell surface markers by immunohistochemistry of murine heart tissues.
BbCRASP expression in cultured spirochetes grown in vitro to a density of 107/ml and in infected murine skin and heart tissue samples at 12 days of infection is presented (Fig. 6).
Here, we characterize the mechanical behavior of tissue simulant gel candidates comprising a chemically crosslinked polydimethylsiloxane (PDMS) network loaded with a non-reactive PDMS solvent, and compare this response with that of tissue from murine heart and liver under comparable loading conditions.
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