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2 protocols using imatinib im

1

Antibodies and Inhibitors for Protein Analysis

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Polyclonal antibodies to KIT (western), MAPK, GAPDH and HSP90 were purchased from Dako (Carpinteria, CA), Life Technologies (Carlsbad, CA), Proteintech Group Inc. (Rosemont, IL) and Santa Cruz Biotechnology (Santa Cruz, CA), respectively. All phospho-antibodies, polyclonal antibodies to AKT and the monoclonal antibody to S6 were purchased from Cell Signaling Technology (Beverly, MA). Monoclonal mouse antibodies to KIT (co-IP) and CK2 (Santa Cruz Biotechnology, CA), CDC37 (Abcam Biotechnology, Cambridge, MA) and β-actin (Sigma-Aldrich, St. Louis, MO) were used. Anti-mouse normal IgG was purchased from Cell Signaling Biotechnology. CX4945 (CX) and imatinib (IM) were purchased from Selleck (Houston, TX) and LC Laboratories (Woburn, MA, USA), respectively. Lentiviral CK2 shRNA constructs were purchased from The RNAi Consortium (TRC, Cambridge, MA, USA). Crystal violet and propidium iodide solution were purchased from Sigma-Aldrich. Protein A, Protein G beads, Lipofectamine and Plus reagent were purchased from Invitrogen (LIFE Technologies, USA). Puromycin and polybrene were purchased from Sigma (St. Louis, MO, USA).
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2

Imatinib, 17-DMAG, and Novobiocin Therapy

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From day 10 after transplantation, the recipient mice were treated once daily with 50 mg/kg imatinib (IM) (S1026; Selleck) in 0.2 mL 0.5% CMC-Na (S6703; Selleck) or 0.5% CMC-Na as a control by gavage. The 17-DMAG was dissolved in 5% DMSO + 40% PEG300 + 5% Tween-80 + 50% water, and novobiocin was dissolved in water. The 17-DMAG (25 mg/kg) and novobiocin (100 mg/kg) were administered by intraperitoneal injection, once daily. The treatments were continued until the recipient mice were euthanized. The weight and appearance of the treated mice were monitored every other day and they were euthanized when they appeared moribund.
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