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Mg 132 z lll cho

Manufactured by Merck Group
Sourced in United States

MG-132 (Z-LLL-CHO) is a proteasome inhibitor, a class of compounds that inhibit the activity of the proteasome, a multi-subunit protein complex responsible for the degradation of cellular proteins. It functions by blocking the chymotrypsin-like activity of the proteasome.

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2 protocols using mg 132 z lll cho

1

Bortezomib and Proteasome Inhibition

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Bortezomib (VELCADE®) was generously provided by Millennium Pharmaceuticals Inc. (Cambridge, MA, USA). MG‐132 (Z‐LLL‐CHO) and Lactacystin was purchased from Sigma Aldrich. Antibodies against human PARP, actin and α‐tubulin were purchased from Santa Cruz biotechnology 37, 38. Sequencing Grade Modified Trypsin V511A was obtained from Promega.
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2

Peptide FRET Substrates for Protease Assays

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Peptide FRET substrates with ten glutamine residues were procured from GenScript (Piscataway, NJ, USA); the substrate with five glutamine residues was purchased from Peptide Protein Research Ltd. (Fareham, UK). The standard fluorescent substrates for proteasome assays (N-succinyl-Leu-Leu-Val-Tyr-7-amino-4-methylcoumarin, Suc-LLVY-AMC) and HIV protease substrate 1 (Arg-Glu(EDANS)-Ser-Gln-Asn-Tyr-Pro-Ile-Val-Gln-Lys(Dabcyl)-Arg) were from Sigma-Aldrich (St. Louis, MO, USA) and Invitrogen (Carlsbad, CA, USA), respectively. Ac-RLR-AMC and Z-LLE-AMC were from UBPBio (Dallas, TX, USA). Bortezomib was from LC Laboratories (Woburn, MA, USA), MG-132 (Z-LLL-CHO), leupeptin (as hemisulfate salt), and marizomib was from Sigma-Aldrich, and Z-P-nLeu-D-CHO was from Enzo Life Science (Farmingdale, NY, USA). All other reagents were of the highest quality available or for molecular biology grades and were used without additional purification.
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