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Cells starved of glucose and/or glutamine for 24–36 hr were stimulated as indicated. Cells were transfected with JetPEI Polyplus reagent (Genycell Biotech) and treated as indicated 24 hr later. |
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Protocol tips |
Cells starved of glucose and/or glutamine for 24–36 hr were stimulated as indicated. Cells were transfected with JetPEI Polyplus reagent (Genycell Biotech) and treated as indicated 24 hr later. |
Publication protocol
Tumor enteroendocrine STC-1, ovary carcinoma OVCAR-3, mammary adenocarcinoma MDA-MB-231, and colorectal adenocarcinoma HT-29 cells were cultured in Dulbecco’s modified Eagle’s medium and pancreatic carcinoma AsPC-1 in RPMI. Both media were supplemented with 10% fetal bovine serum. Cells starved of glucose and/or glutamine for 24–36 hr were stimulated as indicated. Cells were transfected with JetPEI Polyplus reagent (Genycell Biotech) and treated as indicated 24 hr later. Recombinant Wnt-3a proteins were from PeproTech. The GloMax 96 Luminometer (Promega) and Dual-Luciferase kit were used. Fractionation was as in Andrews and Faller (1991).
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Paper title
Glucose-induced β-catenin acetylation enhances Wnt signaling in cancer.
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