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3 protocols using entinostat

1

HDAC Inhibitor and IL-10 Synthesis Modulator Protocols

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Agent MS275, a selective class 1 HDAC inhibitor [13 (link)] (Entinostat, Santa Cruz Biotechnology, sc-279455), was reconstituted to a stock concentration of 10 mM in DMSO. The immunomodulator AS101 (Santa Cruz Biotechnology, sc-203825) that inhibits IL-10 protein synthesis [14 (link)] was reconstituted at a concentration of 5 mM in DMSO.
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2

Probing Neurotrophic Factor Signaling

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Cleavage-resistant mutated form of proNGF (K103A and R104A) was obtained from Alomone Labs (Jerusalem, Israel). Entinostat was obtained from Santa Cruz Biotechnology (Dallas, TX, USA). MC1568 was from SelleckChem (Houston, TX, USA). Romidepsin, PCI-34051, tubacin, 3-deazaneplanocin A hydrochloride (DZNep), and tazemetostat (TZM) were from MedChem Express Europe (Sollentuna, Sweden). VPA, trichostatin A (TSA), sodium butyrate, neurotensin, and 4’,6-diamidino-2phenylindole dihydrochloride (DAPI) were from Sigma-Aldrich (St. Louis, MO, USA).
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3

Evaluation of Pharmacological Inhibitors

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Recombinant human NT-3 was obtained from ImmunoTools (Friesoythe, Germany). Entinostat and PD 98,059 were obtained from Santa Cruz Biotechnology (Dallas, TX, USA). Vorinostat, romidepsin, PCI-34051, tubacin, 3-deazaneplanocin A hydrochloride, (+)-JQ-1 and tazemetostat were obtained from MedChem Express Europe (Sollentuna, Sweden). VPA and 4′,6-diamidino-2phenylindole dihydrochloride (DAPI) were obtained from Sigma-Aldrich (St. Louis, MO, USA). BIRB 0796 was obtained from Axon Medchem BV (Groningen, The Netherlands), whereas TCS JNK6o was from Tocris Bioscience (Bristol, UK).
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