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Also, IGF binding ability was confirmed by western-ligand blot analysis by utilizing DIG-labeled IGF-1 according to previous study [46].
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Western blot analysis was utilized to demonstrate CDC25s expression in vulvar cancer cell lines.
To further understand the molecular mechanisms of ARV S1133-induced andophapoptosispoptosis, co-immunoprecipitation followed by Western blotting analysis was utilized to detect the protein complex formation.
Fractions with the highest antibodies as judged by western blot analysis against TAp63 were utilized for subsequent experiments.
Hence, western blot analysis of MAPKs protein was utilized to study the mechanism by which PTE pre-treatment protects dIMR32 cells against neuronal cell death induced by H2O2.
Northern blot analysis of Atlantic salmon tissues utilized the same probe 1 described for the Southern blot analysis.
However, since anti-CDC25B used for immunohistochemistry was not recommended by the supplier to use for Western blot analysis, an alternative anti-CDC25B was utilized for Western blot analysis.
A western blot analysis of KCNMA1 expression was performed, utilizing the same cell lines previously examined by northern blot (Figure 2B) for KCNMA1 transcript expression.
The karyotypically silent t(4 14) translocation, undetectable by conventional cytogenetic analysis, was identified independently by two groups utilizing southern blot analysis of cell line and patient samples.
The expression level of APP in multiple breast cancer cell lines was measured by Western blot analysis and the breast cancer tissue microarray was utilized to analyze the expression pattern of APP in human patient specimens.
To understand the molecular mechanism of cell cycle regulation by TGFβ1, we utilized western blot analysis.
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