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Phospho s6 ribosomal protein235 236

Manufactured by Cell Signaling Technology
Sourced in China

The Phospho-S6 ribosomal protein235/236 is a specific antibody that recognizes the phosphorylated form of the S6 ribosomal protein at serine residues 235 and 236. This antibody is used to detect and quantify the phosphorylation levels of the S6 ribosomal protein, which is a downstream target of the mTOR signaling pathway and is involved in the regulation of protein synthesis.

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2 protocols using phospho s6 ribosomal protein235 236

1

Intracellular Signaling Pathway Analyses

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NIH 3T3 fibroblasts were obtained from ATCC (Manassas, VA) and maintained in DMEM (HyClone, Logan, UT) supplemented with 10% fetal bovine serum, 100 units/ml penicillin, and 100 µg/ml streptomycin in a 5% CO2 incubator at 37°C. Primary antibodies against phospho-AktS473, phospho-MekS217/221, Pan-Mek, phospho-S6 ribosomal protein235/236, phosphop-70S6KT421/S424, phospho-ERK1/242/44, phospho-4EBP37/46 and pan-Akt were purchased from Cell Signaling (Boston, MA). Primary antibodies against phospho-p70S6KSer411 were purchased from Abcam (Cambridge, MA). Bleomycin and primary antibodies against β-actin and fibronectin were purchased from Sigma (St. Louis, MO). Anti-collagen-I was purchased from Rockland (Gilbertsville, PA). All HRP-conjugated secondary antibodies were obtained from Bio-Rad (Hercules, CA) and Alexa-labelled secondary antibodies were purchased from Life Technologies (Carlsbad, CA). TGFβ was purchased from R&D (Minneapolis, MN), whereas LY294002 inhibitor, U0126 inhibitor, and Rapamycin were purchased from EMD Millipore Bioscience (San Diego, CA). PF4708671 inhibitor was obtained from Santa Cruz Biotechnology (Dallas, TX). Adenoviral particles encoding CA-Mek1 and DN-Mek1 were obtained from Cell Biolabs, Inc. (San Diego, CA), whereas retroviral plasmids encoding CA-Akt1 and DN-Akt1 were generated in the laboratory [6 (link)].
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2

Western Blot Analysis of Cellular Proteins

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Cells were washed two times with pre-chilled phosphate-buffered saline (PBS) and collected with lysis buffer. The protein concentrations of the lysates were detected using the BCA assay. An equivalent of 50  μ g was separated by 12% or 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and then transferred to nitrocellulose membranes. Subsequently, the membranes were blocked with 5% BSA in TBST, followed by incubation with primary antibodies against KLF13 (LifeSpan Biosciences, Seattle, WA), Phospho-Akt-Ser473 (Cell Signaling Technology, Danvers, MA), Akt (Cell Signaling Technology, Danvers, MA), Phospho-S6 Ribosomal Protein (235/236) (Cell Signaling Technology, Danvers, MA), S6 Ribosomal Protein (Cell Signaling Technology, Danvers, MA), PARP1 (Proteintech, Wuhan, China), BAX (Proteintech, Wuhan, China), GAPDH (Santa Cruz Biotechnology, Shanghai, China) at 4 C overnight. Then, the membranes were hybridized with the IRDye secondary antibodies at room temperature for 1.5 h. The immunoreactive bands were visualized using Odyssey Infrared Imaging System (Lincoln, NE, USA).
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