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Renin active IRMA (CT)

Catalog no.MG11101
Regulatory Status
EU: CE
Kit size
96
Method
IRMA (CT)
Incubation time
1 x 3 h
Standard range
4 - 520 pg/mL
Specimen / Volumes
300 µL EDTA Plasma
Substrate / isotope
125I < 760 kBq

Intended Use

Immunoradiometric assay kit for the quantitative determination of active Renin in human EDTA plasma.

Clinical background

Renin, a polypeptidic enzyme (MW~ 40000) also known as angiotensinogenase, is a circulating protease secreted by juxtaglomerular cells in the juxtaglomerular apparatus of the kidneys in response to low blood volume or low body NaCL content.

Renin activates the renin-angiotensin system by cleaving angiotensinogen produced in the liver into angiotensin I (inactive) which is further converted into angiotensin II (active) in the vascular epithelium of the lung. Angiotensin II can cause vasoconstriction by stimulating the central nervous system , in addition it stimulates ADH (antidiuretic hormone) secretion and aldosterone secretion from the adrenal gland. Regulation of blood pressure and renal glomerular filtration control are the most important functions of renin -angiotensin system. Plasmatic concentration of renin is influenced by concentration of circulating angiotensinogen and subsequently the concentration of angiotensin II. High plasmatic levels of angiotensin II reduce renin secretion.(negative feed back).

Determination of renin plasma levels is useful in the diagnosis of hypertension and in the therapeutic follow up of hypertensive patients. Plasmatic concentration of renin decreases in patients with hypertension due to a primary hyperaldosteronism, contrary to renovascular hypertension where concentrations of renin and aldosterone are both elevated.

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.

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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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