MG-132 50mg 50mg | Purity Not Available
Adooq Bioscience
MG-132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 ??M).
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MG-132 25mg 25mg | Purity Not Available
Adooq Bioscience
MG-132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 ??M).
More Information Supplier PageMG-132 10mM * 1mL in DMSO 10mM * 1mL in DMSO | Purity Not Available
Adooq Bioscience
MG-132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 ??M).
More Information Supplier PageMG-132 100mg 100mg | Purity Not Available
Adooq Bioscience
MG-132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 ??M).
More Information Supplier PageMG-132 10mg 10mg | Purity Not Available
Adooq Bioscience
MG-132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 ??M).
More Information Supplier PageTubastatin A HCl 50mg 50mg | Purity Not Available
Adooq Bioscience
Tubastatin A HCl is a potent HDAC inhibitor that demonstrates over more selectivity than all other HDAC isoforms (IC50s >16 uM), excluding HDAC8 (IC50 = 0.9 M).
More Information Supplier PageTubastatin A HCl 25mg 25mg | Purity Not Available
Adooq Bioscience
Tubastatin A HCl is a potent HDAC inhibitor that demonstrates over more selectivity than all other HDAC isoforms (IC50s >16 uM), excluding HDAC8 (IC50 = 0.9 M).
More Information Supplier PageAR-42 50mg 50mg | Purity Not Available
Adooq Bioscience
AR-42 is a novel HDAC inhibitor, exhibits biologic activity against malignant mast cell lines via down-regulation of constitutively activated Kit.
More Information Supplier PageAR-42 5mg 5mg | Purity Not Available
Adooq Bioscience
AR-42 is a novel HDAC inhibitor, exhibits biologic activity against malignant mast cell lines via down-regulation of constitutively activated Kit.
More Information Supplier PageAR-42 25mg 25mg | Purity Not Available
Adooq Bioscience
AR-42 is a novel HDAC inhibitor, exhibits biologic activity against malignant mast cell lines via down-regulation of constitutively activated Kit.
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