Protease Inhibitors and Phosphatase Inhibitors
R&D Systems Leupeptin, CF
A general, reversible cystein protease inhibitor and trypsin-like serine protease inhibitor
Thermo Scientific™ Halt™ Protease and Phosphatase Inhibitor Cocktails
Prevent protein degradation and stabilize phosphorylation with this all-in-one cocktail of protease and phosphatase inhibitors.
Thermo Scientific™ Pierce™ Phosphatase Inhibitor Tablets
Protect serine, threonine and tyrosine phosphorylation in your sample with these broad-spectrum phosphatase inhibitor tablets.
R&D Systems Pepstatin A, CF
A general, reversible inhibitor of aspartyl proteases including renin, pepsin and cathepsin D
Thermo Scientific™ Halt™ Protease Inhibitor Cocktails
Inhibit proteolytic degradation during cell lysis and protein extraction with these ready-to-use concentrated stock solutions of protease inhibitors.
Thermo Scientific™ Pierce™ Protease and Phosphatase Inhibitor Tablets
Ensure complete protection from dephosphorylation and proteolytic degradation with these broad-spectrum protease and phosphatase inhibitor tablets.
Thermo Scientific™ Pierce™ Protease Inhibitors
Customize your protease inhibitor cocktail formulation with these small packages of individual protease inhibitor peptides and compounds.
Thermo Scientific™ Halt™ Phosphatase Inhibitor Cocktail
Stabilize serine, threonine and tyrosine phosphorylation of proteins in cells and tissues with this cocktail of phosphatase inhibitors.
Thermo Scientific™ Pierce™ Protease Inhibitor Tablets
Thermo Scientific™ Pierce Protease Inhibitor Tablets and Mini Tablets are broad-spectrum protease inhibitors that are highly effective at preventing proteolytic degradation for cell lysis and protein extraction experiments.
Thermo Scientific™ Protease Inhibitor Cocktails
Protect your sample from proteolytic degradation during cell lysis with these broad-spectrum protease inhibitor cocktails.
R&D Systems General Caspase Inhibitor Q-VD-OPh
Cell-permeable, irreversible inhibitor of caspase activity. Q-VD-OPh does not exhibit toxic effects at typical working concentrations.
Novex™ SUMO Protease
A recombinant fragment of ULP1 (Ubl-specific protease 1) from Saccharomyces cerevisiae
Invitrogen™ Novex™ AcTEV™ Protease
Specifically recognizes a seven amino acid sequence (Glu-Asn-Leu-Tyr-Phe-Gln-Gly, cleaving between Gln and Gly), ideal for removing affinity tags from fusion proteins
EMD Millipore Calbiochem™ Gabapentin
A water soluble GABA analog that interacts with voltage-gated calcium channels in cortical neurons.
EMD Millipore Calbiochem™ mGluR5 Antagonist, MTEP
The mGluR5 Antagonist, MTEP, also referenced under CAS 329205-68-7, controls the biological activity of mGluR5. This small molecule/inhibitor is primarily used for Neuroscience applications.
EMD Millipore Calbiochem™ Metastin (45-54)
A decapeptide with C-terminally amidated LRF-motif that acts as a potent and selective agonist of AXOR12 and hOT7T175 (a novel human G-protein-coupled receptors).
EMD Millipore Calbiochem™ InhibitorSelect™ p53 Pathway Regulators Panel
The InhibitorSelect™ p53 Pathway Regulators Panel controls the biological activity of InhibitorSelect™. This small molecule/inhibitor is primarily used for Activators/Inducers applications.
EMD Millipore Calbiochem™ InSolution™ Q-VD-OPh, Non-O-methylated
InSolution™ Q-VD-OPh, Non-O-methylated, is a cell-permeable, irreversible, broad-spectrum inhibitor of caspases (IC50 = 50, 100, 430, and <25 nM for caspase-1,-8, -9, and -3, respectively).
EMD Millipore Calbiochem™ 2-Guanidinoethylmercaptosuccinic Acid
Potent inhibitor of a carboxypeptidase B-like processing enzyme referred to as enkephalin convertase (Ki = 8.8 nM).
EMD Millipore Calbiochem™ InSolution™ Tamoxifen, 4-Hydroxy-, (Z)-
A 10 mM (2 mg/516 μL) sterile-filtered solution of (Z)-4-Hydroxytamoxifen in ethanol.
EMD Millipore Calbiochem™ Compound 56
A cell-permeable, reversible, ATP-competitive, highly potent and specific inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (IC50 = 6 pM).
EMD Millipore Calbiochem™ Cytohesin Inhibitor II, Cyplecksin 2
Selectively and covalently modifies the pleckstrin homology domain of the cytohesin family (Kd ≈2 μM to cytohesin-1) and irreversibly inhibits its function.