Western blot analysis confirmed that CHO (Chinese Hamster Ovary) cells do not constitutively express LOX-1 (data not shown).
Western blot analysis confirmed that SPOP overexpression led to a marked increase of TRIM24 ubiquitination (Fig. 3e).
Northern blot analysis confirmed that both hmg1 and hmg2 transcripts possessed a size of 2.4 kb.
Reverse transcription-PCR (RT-PCR) and western blot analysis confirmed that the cloned tissues expressed tissue-specific mRNA and proteins while expressing a different mitochondrial DNA (mtDNA) haplotype.
Western blot analysis confirmed that IFNγ MSA was expressed as a fusion protein, but hardly formed dimer as IFNγ did.
Western blot analysis confirmed that the modified IIIa proteins were expressed in infected cells and incorporated into virions.
Western blot analysis confirmed that the expressions of CAMK4, THEMIS, and CD3G, which were involved in the upregulated pathways, were induced upon PFOS exposure.
Similarly, western blot analysis confirmed that Runx2 and OCN expression was significantly decreased under inflammatory conditions as well as under osteo-inductive conditions with P2X7R antagonist addition (p < 0.001; Fig. 2e, f).
Western blot analysis confirmed that the purified protein was HBD3 (Fig. 2d).
Western Blot analysis confirmed that this purified protein corresponded to VEGF165 (Fig. 3d, lane 2).
Western blot analysis confirmed that the protein abundance of NADPH oxidase subunit p47phox and the AT1 but not the AT2 receptor was enhanced in HG myocytes.
