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Infromación Gnral Reactivos |
Cell Technology fue fundada en 1998 para proporcionar soluciones para la investigación académica, biotecnológica y farmacéutica. Su objetivo es desarrollar ensayos únicos que permiten a los investigadores estudiar las funciones celulares utilizando reactivos que penetran la membrana celular. Este proceso permite la detección in situ de eventos c...
Cell Technology fue fundada en 1998 para proporcionar soluciones para la investigación académica, biotecnológica y farmacéutica. Su objetivo es desarrollar ensayos únicos que permiten a los investigadores estudiar las funciones celulares utilizando reactivos que penetran la membrana celular. Este proceso permite la detección in situ de eventos celulares o de tejidos específicos, asegurando el mantenimiento de la morfología y de la arquitectura. Su primer lanzamiento fue una línea de productos que detectan células apoptóticas mediante la medición de las caspasas activas y la pérdida de potencial de membrana mitocondrial. Se ha ampliado su catálogo con productos altamente específicos de detección de caspasa, así como para la detección de los productos de la catepsina y productos ELISA. Se seguirá ampliando con productos con el compromiso de desarrollar reactivos únicos, de alta tecnología.
A sensitive, one-step, no wash assay for the sensitive monitoring of catalase activity by measuring residual hydrogen peroxide substrate. A non-fluorescent detection reagent generates a fluorescent signal in the presence of peroxidase and resorufin.
A non-radioactive cytotoxicity assay allowing phenotyping of a heterogeneous target cell population and detection of cytolytic activity at the cellular level, using flow cytometry.
A non-fluorescent detection reagent is reduced in the presence of NADPH to produce its fluorescent analog and NADP. NADP is further converted to NADPH via an enzyme-coupled reaction. The kit specifically detects NADP/NADPH and not NAD/NADH.
An oxidation/reduction-based reagent quantitatively measures the reducing power of living cells. The cell-permeable reagent is blue in color, but non-fluorescent. When reduced by viable cells, it fluoresces red. Read in a fluorescent plate reader.
This one step, no-wash assay utilizes a non-fluorescent detection reagent, which is oxidized in the presence of hydrogen peroxide and Eosinophil Peroxidase to produce its fluorescent analog. Read in absorbance or fluorescence formats. HTS adaptable.
A bioluminescence, non-radioactive cytotoxicity assay designed to quantitatively measure the release of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from mammalian cell lines or bacterial cells.
A homogenous fluorescent assay that utilizes the quenched (z-DEVD)2-R110 peptide substrate for caspase 3/7 detection. The assay can be used for high throughput screening
The kit uses a fluorescent readout to specifically detect NAD/NADH, with no reactivity with NADP/NADPH. It is suitable for use with cells and tissue from a range of sources such as animals, plants, bacteria and fungi.
A kit to determine acetylcholinesterase activity in red blood cells, saliva, or lysates using the natural substrate, acetylcholine. In addition, the use of specific inhibitors can be used to detect Ache activity in a variety of samples.
This kit utilizes a cell permeable two-color stain to simultaneously detect caspase activity and mitochondrial membrane potential (MMP) in cells. Active caspase-1 is detected with the caspase probe FAM-YVAD-FMK and MMP with a cationic dye.
A general selective indicator for the detection of highly Reactive Oxygen Species (hROS), such as Hydroxyl Radical (•OH), Peroxynitrite(ONOO-), and hypochlorite (-OCl). It has little reactivity with other ROS.
A rapid and extremely sensitive assay for acetylcholinesterase using the natural substrate acetylcholine. A series of coupled reactions generate a bioluminescent signal. Ideal for identifying and characterizing acetylcholinesterase inhibitors.