Noradrenaline/ Dopamine-Sensitive

Highly sensitive enzyme immunoassay for the quantitative determination of Noradrenaline & Dopamine in urine, plasma, cell culture samples, tissue homogenates and other biological fluids.

Clinical Fields: Endocrinology, Oncology, Psychiatry
Diseases: Pheochromocytoma, neuroblastoma, ganglioneuroma, degenerative cardiac diseases, hyper- and hypotension, schizophrenia, manic-depressive psychosis, stress, burn-out syndrome

Catalog No Size
Product Catalog No: EA631/192 Pack Size: 96 wells

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Summary

Procedure
Sample Preparation 2 hours (Extraction & Acylation), ELISA incubation over night (15 – 20 h)

Characteristics

Highly sensitive ELISA

Small sample volume only (1 – 500 µl)

Sample stabilizer included

For research use only

Test Principle

Catecholamine is the name of a group of aromatic amines (noradrenaline, adrenaline, dopamine, and their derivatives) which act as hormones and neurotransmitter, respectively. Adrenaline and noradrenaline are formed from dopamine. They act on the cardiac musculature and the metabolism (adrenaline) as well as on the peripheral circulation (noradrenaline) and help the body to cope with acute and chronic stress.

An increased production of catecholamines can be found with tumours of the chromaffine system (pheochromocytoma, neuroblastoma, ganglioneuroma). An increased or decreased concentration of the catecholamines can also be found with hypertension, degenerative cardiac diseases, schizophrenia and manic-depressive psychosis.

The assay kit provides materials for the quantitative measurement of noradrenaline and dopamine in low concentrated samples and for small sample volumes. Noradrenaline and dopamine are extracted using a cisdiol-specific affinity gel and acylated to N-acylnoradrenaline and Nacyldopamine and then converted enzymatically into N-acylnormetanephrine and N-acyl-3-methoxytyramine.

The competitive Noradrenaline / Dopamine – Sensitive – ELISA kit uses the microtitre plate format. Noradrenaline and dopamine, respectively, are bound to the solid phase of the microtiter plate. Acylated catecholamine from the sample and solid phase bound catecholamine compete for a fixed number of antiserum binding sites. When the system is in equilibrium, free antigen and free antigen-antiserum complexes are removed by washing. The antibody bound to the solid phase catecholamine is detected by anti-rabbit IgG / peroxidase. The substrate TMB / peroxidase reaction is monitored at 450 nm. The amount of antibody bound to the solid phase catecholamine is inversely proportional to the catecholamine concentration of the sample.

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