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5,5'-(3-Carboxilato-4-oxociclohexa-2,5-dienilidenmetilen)disalicilato de triamonio, en polvo, Sigma-Aldrich®

Numero del catalogo: (A0885-25G)

Proveedor: SIGMA ALDRICH MICROSCOPY

Descripción: Aurintricarboxylic acid ammonium salt has been used as a nuclease inhibitor to study its effects on transfection.

UOM: 1 * 25 g

Promoción

N/A Each

5,5'-(3-Carboxilato-4-oxociclohexa-2,5-dienilidenmetilen)disalicilato de triamonio, Supelco®

Numero del catalogo: (1.00128.0010)

Proveedor: Merck

Descripción: 5,5'-(3-Carboxilato-4-oxociclohexa-2,5-dienilidenmetilen)disalicilato de triamonio, Supelco®

UOM: 1 * 10 g

MSDS Promoción

N/A Each

5,5'-(3-Carboxilato-4-oxociclohexa-2,5-dienilidenmetilen)disalicilato de triamonio ACS, Sigma-Aldrich®

Proveedor: SIGMA ALDRICH MICROSCOPY

Descripción: Reagent for aluminium. Aurintricarboxylic acid readily polymerises in aqueous solution, forming a stable free radical that inhibits protein-nucleic acid interactions. It is a potent inhibitor of ribonuclease and topoisomerase II by preventing the binding of the nucleic acid to the enzyme. It stimulates tyrosine phosphorylation processes including the Jak2/STAT5 pathway in NB2 lymphoma cells, ErbB4 in neuroblastoma cells, and MAP kinases, Shc proteins, phosphatidylinositide 3-kinase and phospholipase C in PC12 cells. Aurintricarboxylic acid inhibits apoptosis in many cell types. Its neuroprotective effect, perhaps due to its ability to prevent down-regulation of Ca²⁺ impermeable GluR2 receptors or to its ability to inhibit calpain, a Ca²⁺-activated protease that is activated during apoptosis.