Calcium test system

A cell-permeable inhibitor of phospholipase A 2 that blocks epinephrine-stimulated thromboxane production in platelets. Inhibits ATP-stimulated phosphatidylcholine (PC) secretion in alveolar type II cells.

A cell-permeable amphiphilic diamine that blocks cholesterol biosynthesis and its esterification. Specifically blocks 7-dehydrocholesterol reductase (&#916 7 -sterol reductase) activity with IC 50 = 13 nM.

This certified reference material (CRM) is produced in accordance with ISO 17034 and characterized in accordance with ISO/IEC 17025. This CRM is traceable to SI unit kg and measured against primary material from a National Metrology Institute

A selective inhibitor of MMP-13 (IC 50 = 10 &#181M) that does not appear to act by chelating Zn 2+ . Binds within the entire S1&#8242 pocket of MMP-13, docking with the morpholine ring adjacent to the catalytic zinc atom.

Polymeric 7.5% cross-linked soft-gel columns for cation, ligand exchange separations of carbohydrates.

A non-ionic surfactant used in the isolation and purification of functional membrane protein complexes and in two-dimensional (2D) gel electrophoresis. Similar in usage to NP-40 and TRITON &#8482 X-100 Detergent(Cat.

A non-ionic surfactant used in the isolation and purification of functional membrane protein complexes and in two-dimensional (2D) gel electrophoresis. Similar in usage to NP-40 and TRITON &#8482 X-100 Detergent(Cat.

A non-ionic surfactant used in the isolation and purification of functional membrane protein complexes and in two-dimensional (2D) gel electrophoresis. Similar in usage to NP-40 and TRITON &#8482 X-100 Detergent(Cat.

A cell-permeable, potent and selective inhibitor of nitric oxide (NO)-sensitive guanylyl cyclase (IC 50 = 20 nM). In incubated cerebellum slices, ODQ reversibly inhibits the NO-dependent cGMP response to glutamate receptor agonists without

Formula: NH₂C(CH₂OH)₃ Formula Weight: 121.14 CAS Number: 77-86-1 Synonym(s): Tris(Hydroxymethyl)Aminomethane

A potent, cell-permeable, reversible, competitive, and selective p38 MAP kinase inhibitor (IC 50 = 89 nM). Inhibition of p38 MAP kinase by PD 169316 blocks apoptosis induced by trophic factor withdrawal in non-neuronal and neuronal cell lines.

A potent, reversible, ATP-competitive, and cell-permeable inhibitor of Src-family tyrosine kinases that is &gt800 times more selective for the I338G mutant v-Src (IC 50 = 1.5 nM) compared to wild-type v-Src (IC 50 = 1.