Name | MG-132 |
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Supplier | Cell Signaling Technology |
Catalog | 2194 |
Prices | $59.00 |
Sizes | 1 mg |
Formula | C26H41N3O5 |
Molecular Weight | 475.6 g/mol |
Purity | >98% |
Description | MG-132 is a potent proteasome and calpain inhibitor. Research studies have shown that MG-132 prevents degradation of the proteasome substrates SucLLVY-MCA and ZLLL-MCA with an IC 50 of 850 nM and 100 nM, respectively, as well as inhibits casein-degrading activity of m-calpain with an IC 50 of 1.25 µM (1). Investigators have demonstrated that MG-132 inhibits TNF-α-induced NF-κB activation and IL-8 release in A549 cells (2). Proteasome inhibition with MG-132 prevents degradation of short-lived proteins, which correlates with increased expression of HSP and ER chaperone proteins (3). MG-132 induces apoptosis in Hep G2 cells in a time- and dose-dependent manner (4). Proteasome inhibitors like MG-132 are important research tools for studying cellular degradation of the ubiquitin-proteasome pathway. |
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