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Cocktails, tablets, capsules, and individual purified formulations of protease inhibitors and phosphatase inhibitors designed to protect proteins from degradation during cell lysis and extraction.
A cell-permeable compound that targets the conserved C-terminal domain of SPAK and OSR1 via reversible binding (Kd = 20 μM; rat SPAK-CCT452-553 GST fusion).
The PPM1D Phosphatase Inhibitor, also referenced under CAS 1087-07-6, controls the biological activity of PPM1D Phosphatase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
The widely used MMP substrate FS-1 is modified by an N-terminal lysine elongation to produce a broad-spectrum MMP and TACE substrate that displays improved water solubility and substrate sensitivities.
A panel containing 14 potent, selective, reversible and cell-permeable inhibitors useful for the study of multiple signaling pathways activated by FGF: 1 mg of Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 (Cat
The Caspase Inhibitor, Negative Control, also referenced under CAS 105637-38-5, controls the biological activity of Caspase. This small molecule/inhibitor is primarily used for Cancer applications.
The S1P1 Receptor Agonist, SEW2871, controls the biological activity of S1P1 Receptor. This small molecule/inhibitor is primarily used for Activators/Inducers applications.
The EGF/FGF/PDGF Receptor Tyrosine Kinase Inhibitor controls the biological activity of EGF/FGF/PDGF Receptor Tyrosine Kinase. Primarily used for Phosphorylation & Dephosphorylation applications.
A highly potent and specific oxysterol EBI2 (GPR183) agonist with a kd of 450 pM in a saturation binding analysis, and activates EBI2 (EC50 140 pM compared wit