Especialista en estudio de funciones celulares, en el desarrollo de productos que detectan células en apoptosis y la pérdida de potencial de membrana mitocondrial
ICT’s Fluoro ATP assay provides a reliable, sensitive fluorimetric assay for the quantification of ATP in biological samples., Detection of ATP in cells or tissue extracts., Detection of ATP in cell death, energy metabolism, mitochondria function., ATP measurement in ATP consuming enzymes such as Kinases and ATPases., ATP detection in Bacterial, Fungal...
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.
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.
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.
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.
Two cell-permeable dyes hydroxyphenyl fluorescein (HPF) and aminophenyl fluorescein (APF) detect hypochlorite production in cells. Hypochlorite production is observed by increased fluorescence of APF loaded cells with no increase in HPF loaded cells.
This kit provides a reliable, sensitive fluorometric method for the quantification of lactate in biological samples such as serum, plasma, urine, and tissue extracts. The assay plate can be incubated and read in 15-30 min.
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.
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.
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.
This kit provides a simple, one-step fluorometric or colorimetric method for determination of phosphate in serum and plasma samples. The assay is based on an enzyme-coupled reaction that detects inorganic phosphate.
This kit provides a reliable, sensitive fluorometric assay for quantifying sarcosine in biological samples. A non-fluorescent detection reagent, is reduced via an enzyme-coupled reaction in the presence of sarcosine to yield a fluorescent product.