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2 protocols using antibody for gapdh

1

Protein Expression Profiling of Oral Cancer Spheres

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Cell lysates were prepared from parental and oralspheres derived from each of Cal27 and OSC19 cell lines. Proteins were separated by SDS-PAGE and transferred onto 0.45 μM nitrocellulose membrane. Membranes were blocked using 5% low fat dry milk in TBST and probed with the following primary antibodies. Proteins were detected using ECL Western Blotting Substrate (Thermo Scientific) and autoradiography. Protein loads were normalized using antibody for GAPDH (Cell Signaling Technologies). The following antibodies were used in this study: Nanog, Notch1, Slug (Cell Signaling Technologies), and c-Fos (Santa Cruz Biotechnology).
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2

Investigating Key Apoptotic Regulators

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The primary antibodies Bax (Cat# AF1020), Bcl-2 (Cat# AF6139), TFAM (Cat# DF3232), and TNF-α (Cat# AF7014) were acquired from Affinity Biosciences (Cincinnati, OH, USA). Antibody for GAPDH (Cat# 2118S) was obtained from Cell Signaling Technology, Inc (Danvers, MA, USA). Antibodies for SIRT1 (Cat# 60303-1-Ig), PGC-1α (Cat# 66369-1-Ig), Nrf2 (Cat# 16396-1-AP), PARP1 (Cat# 13371-1-AP), and Caspase3 (Cat# 19677-1-AP) were purchased from Proteintech Group, Inc (Wuhan, China). Goat anti-rabbit IgG-HRP (Cat# 98164S) and anti-mouse IgG-HRP (Cat# 91196S) were purchased from Cell Signaling Technology, Inc (Danvers, MA, USA) and Proteintech Group, Inc (Wuhan, China), respectively.
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