Article No
AG-CN2-0418-M001
Ionomycin . calcium salt
Ionomycin . calcium salt
Chemicals & Biochemicals
Specifications
| CAS No | 56092-82-1 |
| MW | 707.0 . 40.1 |
| Article No | AG-CN2-0418-M001 |
| Country Availability | SE, FI, DK, NO, IS, EE, LV, LT |
| Description | Ionomycin . calcium salt |
| Supplier | Adipogen Life Sciences |
| Format | Powder |
| Notes | Antibiotic [1]. Potent and highly selective Ca2+ ionophore. Commonly used to modify intracellular calcium levels to study calcium transport across biological membranes and to calibrate fluorescent Ca2+ indicators [2, 3]. Ionomycin also transports Pb2+ and some other divalent cations, as well as several lanthanide series trivalent cations at efficiencies that are greater than or equal to those for Ca2+ [3, 9]. Apoptosis inducer [4, 7]. Induces apoptotic neuronal degeneration in embryonic cortical neurons and cell cycle arrest at G1 phase and induces central demyelination [6]. Used to stimulate the intracellular production of the cytokines, interferon, perforin, IL-2 and IL-4 usually in conjunction with PMA [5, 8]. ADAM10 agonist [10]. Potent inducer of shedding CXCL16 [10]. TREK-1 channels inhibitor [11]. PPARgamma ligand with a unique binding mode. Shows effective glucose-lowering activity in a mouse model of diabetes [12].|Chemical. CAS: 56092-82-1. Formula: C41H70O9 . Ca. MW: 707.0 . 40.1. Isolated from Streptomyces conglobatus. Antibiotic. Potent and highly selective Ca2+ ionophore. Commonly used to modify intracellular calcium levels to study calcium transport across biological membranes and to calibrate fluorescent Ca2+ indicators. Ionomycin also transports Pb2+ and some other divalent cations, as well as several lanthanide series trivalent cations at efficiencies that are greater than or equal to those for Ca2+. Apoptosis inducer. Induces apoptotic neuronal degeneration in embryonic cortical neurons and cell cycle arrest at G1 phase and induces central demyelination. Used to stimulate the intracellular production of the cytokines, interferon, perforin, IL-2 and IL-4 usually in conjunction with PMA. ADAM10 agonist. Potent inducer of shedding CXCL16. TREK-1 channels inhibitor. PPARgamma ligand with a unique binding mode. Shows effective glucose-lowering activity in a mouse model of diabetes. |
| Molecular Formula | C41H70O9 . Ca |
| Alias Names | Antibiotic SQ 23377; EM 94 |
| Product Type | Chemicals & Biochemicals |
| Purity | >98% |
| Research area | Metabolism |
| Shipping Information | RT |
| Size | 1 mg |
| Solubility | Soluble in DMSO, ethanol or methanol. |
| Stability | Stable for at least 2 years after receipt when stored at -20°C. |
| Storage | -20°C, 4°C |
| Technical Specifications | Chemical. CAS: 56092-82-1. Formula: C41H70O9 . Ca. MW: 707.0 . 40.1. Isolated from Streptomyces conglobatus. Antibiotic. Potent and highly selective Ca2+ ionophore. Commonly used to modify intracellular calcium levels to study calcium transport across biological membranes and to calibrate fluorescent Ca2+ indicators. Ionomycin also transports Pb2+ and some other divalent cations, as well as several lanthanide series trivalent cations at efficiencies that are greater than or equal to those for Ca2+. Apoptosis inducer. Induces apoptotic neuronal degeneration in embryonic cortical neurons and cell cycle arrest at G1 phase and induces central demyelination. Used to stimulate the intracellular production of the cytokines, interferon, perforin, IL-2 and IL-4 usually in conjunction with PMA. ADAM10 agonist. Potent inducer of shedding CXCL16. TREK-1 channels inhibitor. PPARgamma ligand with a unique binding mode. Shows effective glucose-lowering activity in a mouse model of diabetes. |
| Product Page Updated | 2024-02-01T08:25:01.492Z |
