Cromatest

Extrawash cuvettes solution should be used on board KROMA automatic analyzers for additional cuvette washing.

Systemic solution should be used to prepare the systemic solution for the general washing of cuvettes and needles used in KROMA automatic analyzers.

Cleaning solution for the routine washing application of the automatic Clinical Chemistry instrument LIDA 500 for its internal washing and cleaning.

Extrawash cuvettes solution should be used on board LIDA 500 automatic analyzers for additional cuvette washing.

Surfactant solution for routine cleaning of automatic

C3 at is a turbidimetric assay for the quantification of the C3 component of complement in human serum or plasma. Human anti-C3 antibodies form immune complexes with the C3 complement present in the patient's sample

Urea is hydrolysed by urease to ammonia and carbon dioxide. Ammonia is converted to glutamate by glutamate dehydrogenase (GlDH) in the presence of NADH and ketoglutarate. The reaction is measured kinetically at 340 nm through the decrease in absorbance resulting from the oxidation of NADH to NAD+, proportional to the concentration of urea present in the sample.

Urea is hydrolysed by urease to ammonia and carbon dioxide. Ammonia is converted to glutamate by glutamate dehydrogenase (GlDH) in the presence of NADH and ketoglutarate. The reaction is measured kinetically at 340 nm through the decrease in absorbance resulting from the oxidation of NADH to NAD+, proportional to the concentration of urea present in the sample.

Urea is hydrolysed by urease to ammonia and carbon dioxide. Ammonia is converted to glutamate by glutamate dehydrogenase (GlDH) in the presence of NADH and ketoglutarate. The reaction is measured kinetically at 340 nm through the decrease in absorbance resulting from the oxidation of NADH to NAD+, proportional to the concentration of urea present in the sample.

Uric acid is oxidised by the action of uricase to allantoin and hydrogen peroxide. In the presence of peroxidase (POD) the mixture of dichlorophenol sulphonate (DCBS) and 4-aminoantipyrine (4-AA) are condensed by the action of hydrogen peroxide, forming a coloured quinonaimine proportional to the concentration of uric acid in the sample.

Uric acid is oxidised by the action of uricase to allantoin and hydrogen peroxide. In the presence of peroxidase (POD) the mixture of dichlorophenol sulphonate (DCBS) and 4-aminoantipyrine (4-AA) are condensed by the action of hydrogen peroxide, forming a coloured quinonaimine proportional to the concentration of uric acid in the sample.

Uric acid is oxidised by the action of uricase to allantoin and hydrogen peroxide. In the presence of peroxidase (POD) the mixture of dichlorophenol sulphonate (DCBS) and 4-aminoantipyrine (4-AA) are condensed by the action of hydrogen peroxide, forming a coloured quinonaimine proportional to the concentration of uric acid in the sample.