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Gel shift and luciferase reporter assays were performed to examine the activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) and Toll-like-receptor 4 (TLR4).
In this manuscript, we examine the activation of these composites by performing analytical, numerical, and experimental studies of the temperature distribution, thermal history, and phase transition.
More specifically we examine the activation of water over Pt, PtRu, and Ru surfaces in the presence as well as the absence of solution.
Western blotting of cell lysates with anti-phosphated-Smad2/3 and anti-total Smad2/3 antibodies was performed to examine the activation of TGF-β pathway.
We used Fos-immunoreactivity (Fos-IR) to examine the activation of several subregions of the HPC and striatum in ovariectomized female rats with or without estradiol replacement 30 min after place or response learning.
Six animals were used to examine the activation of the brain and at six time points after the injection blood was taken to measure the response of corticosterone.
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Indeed, our study is limited as we have not examined the activation of stress-activated protein kinase/jun N-terminal kinase by IL-1, TNF-α or APS.
The activity of BRAFV600E was confirmed by examining the activation of ERK1/2 using an antibody against phosphorylated ERK1/2 (Figure 2A).
To confirm our hypothesis that SIRT1 promotes cell proliferation by activating some kinase signaling, we examined the activation of ERK, AKT and p70 S6K1 in different batches of transformations.
To further determine whether the dimerization of Fu is sufficient to activate the Hh pathway, we examined the activation of the Hh pathway by dimerized Fu in vivo.
To determine whether MAPK kinase signaling pathway was activated after liver transplantation, we examined the activation of JNK1/2 and p38 MAPK.
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