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Pf364402

Manufactured by Merck Group
Sourced in United States

PF364402 is a lab equipment product from Merck Group. It is a compact and versatile device designed for laboratory use. The core function of this product is to perform specific tasks required in a research or testing environment. However, a detailed description of its intended use or capabilities cannot be provided in an unbiased and factual manner without the risk of interpretation or extrapolation.

Automatically generated - may contain errors

3 protocols using pf364402

1

Evaluating Cell Death Pathways

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Tert-butyl hydroperoxide (t-BHP, #A13926) was purchased from Alfa Aesar, MAPKAPK2 inhibitor PF-364402 (#PZ0188) and H2O2 (#H1009) from Sigma, AMZ30 (#539695) from Millipore, Z-VAD-FMK (#S8102) from Bio-Connect and necrostatin-1 (#T1547) from Tebubio.
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2

Evaluating MK2 Inhibitor in Murine Tumor Model

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CT26 cell were purchased from ATCC (Manassas, VA). Cells were cultured in complete RPMI with 5% FBS, 1% penicillin/streptomycin, and 1% L-glutamine. CT26 cells were treated for 48 hours before injection with either 50uM of MK2 inhibitor PF364402 (Sigma Aldrich, St. Louis, MO) or DMSO vehicle control. Cells were injected at 105 in 50μl of PBS into the flank of 6–8 week old Balb/c mice. Some mice injected with cells exposed to MK2 inhibitors were treated with recombinant IL-1β, IL-6, and TNFα to replenish cytokine production in amounts of, 25 ng of IL-1β (Biolegend, San Diego, CA), 25 ng of TNFα (Biolegend), and 1 μg of IL-6 (Shenandoah, Warwick, PA). Treatments were administered 3 times/week from day 2 until day 13.
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3

Investigating the Role of MK2 Inhibitor in Tumor Progression

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CT26 cells were purchased from ATCC (Manassas, VA, USA) and MC38 cells were obtained from NIH. Cells were cultured in complete RPMI with 10% FBS, 1% penicillin/streptomycin, and 1% l-glutamine. CT26 or MC38 cells were treated for 48 h before injection with either 50 μM of MK2 inhibitor PF364402 (Sigma Aldrich, St. Louis, MO, USA) or DMSO vehicle control. Cells were injected at 105 for CT26 and 2 × 106 for MC38 in 100 µl of PBS into the flank of 6- to 8-week-old Balb/c mice or C57/Bl6 mice. Some mice injected with cells exposed to MK2 inhibitors were injected intratumorally with recombinant MCP-1 (800 ng), Mip-1α (50 ng), and Mip-2α (700 ng) in 100 µl of PBS to replenish cytokine production or vehicle control. Treatments were administered 3 times/week from day 2 until day 13. Tumors were measured using calipers and divided for culture and RNA work.
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