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cAMP Radioimmunoassay

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Catalog no.RE11021
Regulatory Status
EU: CE, CDN: IVD
Kit size
100
Method
RIA (DAK)
Incubation time
1 x 20 h
Standard range
0.05 - 15 pmol/mL acetylation, 1.5 - 450 pmol/mL without acetylation
Specimen / Volumes
20 µL acetyl. plasma, urine, cell and tissue suspension
Substrate / isotope
125I ≤ 150 kBq

Radio immunoassay for the in-vitro diagnostic quantitative determination of cAMP in human plasma and urine. The test can also be used for non-clinical applications in other biological material. Cyclic adenosin-3',5'-monophosphate (cAMP) serves as a second messenger in signal transduction of various hormones, like adrenaline, ACTH, LH, FSH, glucagon and calcitonin. The hormone itself is the first messenger, binding to specific membrane receptors of hormone-responsive cells. This leads to the activation of an enzyme located at the inner side of the cell membrane, called adenylate cyclase, which catalyses the synthesis of cAMP from ATP. The increased cellular level of cAMP initiates the activation of protein kinases. The determination of cAMP in urine (or plasma) has become more and more important in the clinical assessment of parathyroid functions. The parathyroid hormone (PTH) stimulates the synthesis of cAMP in the renal cortex and an increased secretion of cAMP. The nephrogenic cAMP is a specific marker of circulating PTH: 90 % of patients with hyperparathyroidism show increased levels of nephrogenic cAMP. The determination of nephrogenic cAMP is also significant for the differential diagnosis of hypercalcemia. Urinary levels of cAMP support the diagnosis of hypoparathyroidism and pseudohypoparathyroidism: The administration of PTH to patients with pseudohypoparathyroidism does not lead to an increased cAMP secretion, which is indicative of a defective adenylate cyclase in the renal cortex. Total urinary cAMP levels comprise the nephrogenic cAMP and the plasma cAMP which is not resorbed in the kidneys. In most cases the determination of total urinary cAMP is sufficient, because the concentration of plasmatic cAMP is more or less constant.

For concrete data please consult the Instruction for Use in the download box on the top right side.

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Our comprehensive immunoassay portfolio includes a number of specialty diagnostic immunoassays for endocrinology, immunology and autoimmunity, as well as for diagnosis of multiple infectious diseases. We are pioneers and market leaders in saliva diagnostics, with over 40 years of experience supplying a broad portfolio of luminescence- and ELISA-based tests, including our highly acclaimed HMGB1 and MuSK-Ab ELISAs.

And as experts in laboratory automation, we can support our customers with the protocols for open ELISA platforms, such as the Freedom EVOlyzer or Thunderbolt®.

All products are only available for sale to laboratory professionals and may not be available in all countries. Availability and regulatory status may vary across regions depending on local country-specific registration. Please always read and follow the instructions for use. 

All of our assays have been designed and manufactured to meet the highest global regulatory requirements and quality standards. Tecan is certified under ISO 9001:2015, ISO 13485:2016 and is audited by a notified body according to Medical Device Single Audit Program (MDSAP).

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As part of the Tecan Group, we have a leading market position in diagnostics and research, with over 40 years of experience in the development, manufacture and supply of enzyme-, radiolabel- and luminescence-based immunoassays.

Our range of high-quality immunoassays is supported by a diverse portfolio of automated solutions, making us the perfect partner for you and your customers.

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