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Protease Inhibitors and Phosphatase Inhibitors

Cocktails, tablets, capsules, and individual purified formulations of protease inhibitors and phosphatase inhibitors designed to protect proteins from degradation during cell lysis and extraction.
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631 – 645 of 3,680 results
631

MilliporeSigma™ Calbiochem™ CL316243 Hydrate

A very potent agonist highly selective for β3 adrenoceptors (EC50 =

632

MilliporeSigma™ Calbiochem™ Trichostatin A, Streptomyces sp.

A potent and reversible, cell-permeable inhibitor of histone deacetylase.

633

MilliporeSigma™ Calbiochem™ TRPC3 Channel Inhibitor III, Pyr10

A cell-permeable pyrazole derivative that acts as a selective blocker of the transient receptor potential cation channel TRPC3-medated ROCE (receptor-operated Ca2+ entry) and inhibits Carbachol- (

634

MilliporeSigma™ Calbiochem™ TrpA1 Antagonist, HC-030031

The TrpA1 Antagonist, HC-030031, also referenced under CAS 349085-38-7, controls the biological activity of TrpA1. This small molecule/inhibitor is primarily used for Neuroscience applications.

635

MilliporeSigma™ Calbiochem™ Ubiquitin Aldehyde

Potent and specific inhibitor of multiple ubiquitin hydrolases involved in pathways of intracellular protein modification and turnover.

636

MilliporeSigma™ Calbiochem™ Ursolic Acid

A cell-permeable plant-derived pentacyclic triterpene acid that displays anti-inflammatory, immunomodulatory, and antitumor activities.

637

MilliporeSigma™ Calbiochem™ InSolution™ AG490

Potent inhibitor of epidermal growth factor receptor kinase autophosphorylation (IC50 = 100nM)

638

MilliporeSigma™ Calbiochem™ AG 1295

A cell-permeable, reversible, ATP-competitive, and selective inhibitor of platelet-derived growth factor (PDGF) receptor kinase (IC50 = 500nM) and PDGF-dependent DNA synthesis (IC50 = 2.5μM) in Swiss/3T3 cells.

639

MilliporeSigma™ Calbiochem™ Urokinase Substrate III, Fluorogenic

Suitable for the quantitative direct fluorescent assay of urokinase.

640

MilliporeSigma™ Calbiochem™ InSolution™ Y-27632 in DMSO

InSolution™ Y-27632 is a 10mm solution in DMSO. A highly potent, cell-permeable, reversible, and selective inhibitor of Rho-associated protein kinases (Ki = 140nM for p160ROCK).

642

MilliporeSigma™ Calbiochem™ Iron Chelator IV, 21H7

The Iron Chelator IV, 21H7 controls the biological activity of iron-regulated enzymes. This small molecule/inhibitor is primarily used for Cancer applications.

643

MilliporeSigma™ Calbiochem™ Wortmannin

Wortmannin, CAS 19545-26-7, is a cell-permeable, potent, selective, and irreversible inhibitor of PI3-Kinase (IC50 = 5 nM). Does not affect any upstream signaling events.

644

MilliporeSigma™ Calbiochem™ Wnt/β-catenin Inhibitor, Cardamonin

The Wnt/β-catenin Inhibitor, Cardamonin, also referenced under CAS 19309-14-9, controls the biological activity of Wnt/β-catenin. This small molecule/inhibitor is primarily used for Cancer applications.