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MetCombi Plasma ELISA (Metanephrine / Normetanephrine)

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Catalog no.RE59202
Regulatory Status
EU: CE
Kit size
2 x (12 x 8)
Method
ELISA
Incubation time
1 x 1h, 1 x 2h, 2 x 30min
Standard range
MN: 0 - 2500 pg/mL; NMN: 0 - 3000 pg/mL
Specimen / Volumes
50 µl Plasma EDTA
Substrate / isotope
TMB 450nm

Fast and reliable assay for assessing plasma free metanephrines

Enzyme immunoassay for the quantitative determination of free metanephrine and normetanephrine in human plasma.

Catecholamines and their metabolites, metanephrine and normetanephrine, are secreted in excessive amount by various tumors, including paraganglioma, neuroblastoma, and in particular pheochromocytoma. The clinical manifestation of these tumors is highly variable and often resembles symptoms associated with common maladies, predominantly hypertension, headache and sweating.

Biochemical testing for pheochromocytoma is indicated not only in symptomatic patients, but also in patients with adrenal incidentalomas or identified genetic predispositions. It involves measurements of catecholamines (adrenaline, noradrenaline and dopamine) and their metabolites (metanephrine, normetanephrine and vanillylmandelic acid) in plasma or urine.

Numerous studies have shown that free metanephrines in plasma are the best markers for the diagnosis of pheochromocytomes (Grossmann et al, 2006; Lenders et al., 2005; Eisenhofer et al., 2000)

SensitivitySpecificity
Plasma–free metanephrines99%89%
Urinary–fractionated metanephrines97%69%
Urinary catecholamines86%88%
Plasma catecholamines84%83%
Total urinary metanephrines77%93%
Vanillylmandelic acid (VMA)64%95%
Table 1
Lenders et al. Lancet (2005)

IBL International’s MetCombi Plasma ELISA has been improved

  1. Shorter assay time: ca. 4.5 h
  2. Calibrated to LC–MS/MS
  3. Automated test procedure (DSX)
  4. Smaller sample volume: 200 µL
  5. Higher sensitivity:
       Metanephrine: 7pg⁄mL
       Normetanephrine: 7pg/mL
Corrolation IBL MetcombiCorrolation IBL Metcombi
Fig.1
IBL International MetCombi Plasma ELISA correlates well to LC–MS⁄MS.
Manual and automated IBL MetCombiManual and automated IBL MetCombi
Fig. 2
The manual and automated performances of IBL International MetCombi ELISA correlate well.


Excerpt from the Instructions for Use

Enzyme immunoassay for the quantitative determination of free metanephrine and normetanephrine in human plasma. The catecholamines adrenalin, noradrenalin and dopamine are synthesized in the adrenal medulla, the sympathetic nervous system and in the brain. They influence virtually all tissues and are involved together with other hormonal and neuronal systems in the regulation of a wide variety of physiological processes.

As catecholamines and their metabolites metanephrine and normetanephrine are secreted in increasing amounts in a number of diseases, they may be used for diagnostic purposes.

In this context, diagnosis as well as the follow-up of tumor diseases of the nervous system are of special importance. This applies primarily to the pheochromocytoma, but also the neuroblastoma and the ganglioneuroma.

Malignant growth is described in 10 % of pheochromocytomas. Furthermore, an increase of catecholamines and their metabolites metanephrine and normetanephrine can be observed in the carcinoid.

Data of the last years have shown that the metanephrines in plasma are the best marker for diagnosis and follow-up of pheochromocytoma.

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.

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