524628
Phosphatase Inhibitor Cocktail IV
liquid, for the inhibition of serine/threonine and alkaline phosphatases
Sinónimos:
Phosphatase Inhibitor
Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
About This Item
Código UNSPSC:
12352200
NACRES:
NA.54
Formulario:
liquid
temp. de almacenamiento:
−20°C
Productos recomendados
Nombre del producto
Phosphatase Inhibitor Cocktail Set IV, Phosphatase inhibitor Cocktail Set IV is a cocktail of three phosphatase inhibitors for the inhibition of both serine/threonine and alkaline phosphatases.
Formulario
liquid
fabricante / nombre comercial
Calbiochem®
condiciones de almacenamiento
OK to freeze
protect from light
Condiciones de envío
wet ice
temp. de almacenamiento
−20°C
Descripción general
A cocktail of three phosphatase inhibitors for the inhibition of both serine/threonine and alkaline phosphatases. Available as a 1 ml vial or as a set of five 1 ml vials. Each vial contains a 1 ml solution with the following components: 500 µM Cantharidin (Cat. No. 210155), 2.5 mM (-)-p-Bromotetramisole oxalate, and 1 µM Calyculin A, Discodermia calyx (Cat. No. 208851).
A cocktail of three phosphatase inhibitors specially formulated for inhibition of alkaline phosphatases as well as serine/threonine protein phosphatases such as PP1 and PP2A. May be used with cell lysates and tissue extracts, including extracts containing detergents. Supplied as 1 ml or a set of five 1 ml vials. Each vial contains 1 ml phosphatase inhibitor cocktail solubilized in 95% DMSO, consisting of the following components:
Acciones bioquímicas o fisiológicas
Cell permeable: no
Primary Target
Serine/threonine and alkaline phosphatases
Serine/threonine and alkaline phosphatases
Product does not compete with ATP.
Reversible: no
Advertencia
Toxicity: Highly Toxic (H)
Forma física
In 95% DMSO.
Reconstitución
For long-term storage, aliquot and freeze (-20°C). Dilute 1:50 just prior to use.
Información legal
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 1
Punto de inflamabilidad (°F)
188.6 °F - (refers to pure substance)
Punto de inflamabilidad (°C)
87 °C - (refers to pure substance)
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Los clientes también vieron
Stephane Angers
Methods in molecular biology (Clifton, N.J.), 468, 223-230 (2008-12-23)
Multiple screens performed in Drosophila, Caenorhabditis elegans, Xenopus, and zebrafish have identified dozens of proteins participating in Wnt signal transduction. Epistasis experiments, enhancer and suppressor screens, and protein-protein interaction techniques have also been efficient at finding new pathway members, connecting
Jooyoung Lim et al.
International journal of stem cells, 17(3), 284-297 (2024-04-12)
Acetaldehyde dehydrogenase 2 (ALDH2) is the second enzyme involved in the breakdown of acetaldehyde into acetic acid during the process of alcohol metabolism. Roughly 40% of East Asians carry one or two ALDH2*2 alleles, and the presence of ALDH2 genetic
Chunwan Lu et al.
Oncogene, 41(18), 2651-2662 (2022-03-31)
The role of glucose-6-phosphate dehydrogenase (G6PD) in human cancer is incompletely understood. In a metabolite screening, we observed that inhibition of H3K9 methylation suppressed aerobic glycolysis and enhances the PPP in human mesothelioma cells. Genome-wide screening identified G6PD as an
Heeju Han et al.
Scientific reports, 12(1), 6416-6416 (2022-04-21)
Post-inflammatory hyperpigmentation is a skin discoloration process that occurs following an inflammatory response or wound. As the skin begins to heal, macrophages first exhibit a proinflammatory phenotype (M1) during the early stages of tissue repair and then transition to a
T Pulinilkunnil et al.
International journal of obesity (2005), 38(2), 205-215 (2013-07-03)
Although obesity increases the risk of developing cardiomyopathy, the mechanisms underlying the development of this cardiomyopathy are incompletely understood. As obesity is also associated with increased intramyocardial triacylglycerol (TAG) deposition, also referred to as cardiac steatosis, we hypothesized that alterations
Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.
Póngase en contacto con el Servicio técnico