Calcitonin test system

A cell-permeable benzodiazepine compound that binds the tandem bromodomains of BET (bromodomain and extra terminal domain) family members BRD2 (1-473), BRD3 (1-434), and BRD4 (1-477) with high affinity ( K d = 61.3, 50.

A cell-permeable, reversible and competitive inhibitor of rat brain CaM kinase II (K i = 370 nM). Selectively binds to the CaM binding site of the enzyme and prevents the association of CaM with CaMKII.

A cell-permeable, reversible and competitive inhibitor of rat brain CaM kinase II (K i = 370 nM). Selectively binds to the CaM binding site of the enzyme and prevents the association of CaM with CaMKII.

A potent, specific, cell-permeable, reversible and ATP-competitive inhibitor of protein kinase A (K i = 56 nM) that is prepared by a chemical modification of K-252a. Does not significantly affect the activities of PKC, PKG, and MLCK.

A potent, specific, cell-permeable, reversible and ATP-competitive inhibitor of protein kinase A (K i = 56 nM) that is prepared by a chemical modification of K-252a. Does not significantly affect the activities of PKC, PKG, and MLCK.

A cell-permeable phenoxyacetic acid derivative that acts as a potent and selective peroxisome proliferator activator receptor &#948 (PPAR&#948) agonist (K i = 6 nM for hPPAR &#948 and 730 nM for hPPAR&#947). Induces adipocyte differentiation in

A free radical scavenger and antioxidant that reduces post-ischemic brain injury. Inhibits iron-dependent peroxidation in rat brain homogenates (IC 50 = 15 &#181M).

A cell-permeable, orally active NSAID (nonsteroidal antiinflammatory drug) that blocks cellular Cox pathway PGE2 (prostaglandin E 2 ) production by inhibiting COX-1 and mPGES-1 (microsomal PGE 2 synthase-1), but not COX-2, activity (IC 50 = 8, 2,

Cell-permeable superoxide dismutase (SOD) mimetic. Catalyzes the dismutation of O 2 &#8211 &#8226 (rate constant ~4 x 10 7 M -1 s -1 ) even in the presence of excess EDTA.

Membrane-permeable yellow dye that is reduced by mitochondrial reductases in living cells to form the dark blue product, MTT-formazan. Spectrophotometric measurement of MTT-formazan at 540 or 570 nm allows quantitation of cell viability.

Membrane-permeable yellow dye that is reduced by mitochondrial reductases in living cells to form the dark blue product, MTT-formazan. Spectrophotometric measurement of MTT-formazan at 540 or 570 nm allows quantitation of cell viability.

Suitable for a wide range of molecular biology applications. Molecular biology grade.