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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.
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 Serine/Threonine Kinase Inhibitor Set controls the biological activity of Serine/Threonine Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
The VEGFR2 Kinase Inhibitor III, also referenced under CAS 204005-46-9, controls the biological activity of VEGFR2 Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
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 EGF/FGF/PDGF Receptor Tyrosine Kinase Inhibitor controls the biological activity of EGF/FGF/PDGF Receptor Tyrosine Kinase. Primarily used for Phosphorylation & Dephosphorylation applications.
The Bcl-2 Inhibitor III, EM20-25, also referenced under CAS 141266-44-6, controls the biological activity of Bcl-2. This small molecule/inhibitor is primarily used for Activators/Inducers applications.
The Casein Kinase II Inhibitor VI, TMCB, also referenced under CAS 905105-89-7, controls the biological activity of Casein Kinase II. This small molecule/inhibitor is primarily used for Phosphorylation and Dephosphorylation applications.
A naturally occurring cell-permeable Chaetomium fungal epi-dithio-diketopiperazine that potently inhibits the H3K9 histone methyltransferase activity of Drosophila melanogaster SU(VAR)3-9 and its human homologue SUV39H1 (IC50 = 600 and 800 nM, respectively) in a SAM-competitive manner, while exhibiting much reduced potency against murine G9a or Neurospora crassa DIM5 H3K9 HMT (IC <sub
The S1P1 Receptor Agonist, SEW2871, controls the biological activity of S1P1 Receptor. This small molecule/inhibitor is primarily used for Activators/Inducers applications.
A highly potent and selective CAAX peptidomimetic of the carboxyl terminal of Ras proteins that inhibits farnesyl transferase (FTase) in vitro (IC50 = 500 pM).
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