![]() |
Link a Tocris |
![]() |
Información esencial Tocris |
![]() |
Posters y Guias Tocris |
![]() |
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.
This kit measures monoamine oxidase activity using a non-fluorescent detection reagent to measure H2O2 produced from the conversion of a substrate to its aldehyde via MAO-A/B. The H2O2 oxidizes the reagent to the fluorescent product resorufin.
This kit utilizes a cell permeable two-color stain to simultaneously detect caspase activity and mitochondrial membrane potential (MMP) in cells. Active caspase-3 and -7 are detected with the caspase probe FAM-DEVD-FMK and MMP with a cationic dye.
The kit utilizes a non-fluorescent detection reagent, which is reduced in the presence ADP and a coupled enzyme reaction to produce its fluorescent analog. The kit can be used with mammalian cells and tissues, and bacterial, fungal and plant cells.
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.
Flo200-2 is an easy to use kit which measures mitochondrial membrane potential using flow cytometry. Useful for analysing both suspension and monolayer adherent cell lines.
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.
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.
A simple one step assay which can be used either as a Fluorometric or Colorimetric assay to detect the level of total cholesterol in samples. Cholesterol esters are hydrolyzed by cholesterol esterase. Cholesterol is detected via cholesterol oxidase.
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.
Commercially available ADP is contaminated with trace amounts of ATP. In bioluminescence assays this trace ATP contamination results in high backgrounds and reduces assay sensitivity. ICT's ADP is purified to remove these trace ATP contaminants and as a result produces ADP that is greater than 99.9% pure.
A sensitive kit to detect myeloperoxidase activity in neutrophils and macrophages as well as detecting PMN infiltration in tissue samples. Enables monitoring of multiple time points to follow kinetics and is adaptable to high throughput screening.