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Glucagon ELISA

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Catalog no.30227003
Regulatory Status
RUO
Kit size
12x8
Method
ELISA
Incubation time
overnight; 60 minutes
Standard range
0.31 - 20 pmol/L
Specimen / Volumes
EDTA-plasma
Substrate / isotope
TMB
instructions for use

Glucagon ELISA

Glucagon is a peptide hormone secreted from the alpha cells of the pancreatic islets of Langerhans. The peptide consists of 29 amino acid residues and derives from the precursor proglucagon. (1) As a counterregulatory hormone for insulin, glucagon plays a critical role in maintaining glucose homeostasis in vivo in both animals and humans by stimulating hepatic glucose production. (1, 2) Glucagon acts as a glucose-mobilizing hormone. High plasma glucose concentrations stimulating insulin secretion from pancreatic beta cells, inhibit glucagon secretion whereas low plasma glucose concentrations represent one of the most potent glucagon secretory stimuli. (1) Hypoglycemia (low glucose level) is physiologically the most potent secretory stimulus and the best-known action of glucagon. It stimulates glucose production in the liver and thereby enables adequate plasma glucose concentrations. (1) Glucagon has a crucial role in the pathophysiology of diabetes, obesity and hepatic steatosis, which is discussed vastly in the literature. (1, 4) Proglucagon is a precursor of glucagon, which via post-translational processes produces various peptides like glicentin and oxyindomodulin which have distinct and complementary biological functions. (3) Therefore, an overlap in sequences exists. For example, is the mature form of glicentin composed of 69 amino acids and contains the entire sequences of glucagon and oxyntomodulin. (4) Therefore, the use of an assay system which specifically detects glucagon and does not cross reacts to similar peptides for accurately evaluating glucagon in blood, is required. The Glucagon ELISA kit can specifically measure glucagon produced in α-cells of pancreas by combining antibodies that recognize both the C-terminus and the N-terminus.

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

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

1. Rix Brooks, B., Wood, J. H., Diaz, M., Czerwinski, C., Georges, L. P., Sode, J., ... & Engel, W. K. (1980). Extracellular cyclic nucleotide metabolism in the human central nervous system. Neurobiology of Cerebrospinal Fluid 1, 113-139.

2. Jiang, G., & Zhang, B. B. (2003). Glucagon and regulation of glucose metabolism. American Journal of Physiology-Endocrinology And Metabolism, 284(4), E671-E678.

3. Lee, Y. H., Wang, M. Y., Yu, X. X., & Unger, R. H. (2016). Glucagon is the key factor in the development of diabetes. Diabetologia, 59, 1372-1375.

4. Raffort J, Lareyre F, Massalou D, Fénichel P, Panaïa-Ferrari P, Chinetti G. Insights on glicentin, a promising peptide of the proglucagon family. Biochem Med (Zagreb). 2017 Jun 15;27(2):308-324. doi: 10.11613/BM.2017.034. PMID: 28736498; PMCID: PMC5508206.

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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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