A convenient ready-to-use form of Cycloheximide (Cat. No. 239763). An anti-fungal antibiotic that inhibits protein synthesis in eukaryotes but not in prokaryotes. Interacts directly with the translocase enzyme, interfering with the translocation step. Also inhibits cell-free protein synthesis in eukaryotes. Competitively inhibits hFKBP12 (Ki = 3.4 µM). Triggers apoptosis in HL-60 cells, T-cell hybridomas, Burkitt′s lymphoma cells, and a variety of other cell types, including rodent macrophages. Induces DNA fragmentation in macrophages, but inhibits DNA cleavage in rat thymocytes treated with thapsigargin, methylprednisolone, and ionomycin. Rapidly destroyed in alkaline solutions.
A 100 mg/ml solution of Cycloheximide (Cat. No. 239763) in DMSO (sterile-filtered).
再構成
Following initial use, aliquot and refrigerate (4°C).
その他情報
Christner, C., et al. 1999. J. Med. Chem.42, 3615. Lu, Q. and Mellgreen,R.L. 1996. Arch. Biochem. Biophys.334, 175. Chow, S.C., et al. 1995. Exp. Cell Res.216, 149. Waring, P. 1990. J. Biol. Chem.265, 14476. Obrig, T.G., et al. 1971. J. Biol. Chem.246, 174. Pestka, S. 1971. Annu. Rev. Microbiol.25, 487.
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法的情報
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
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