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Equine Glucagon Like Peptide 1 (GLP1) ELISA Kit-Competitive

Cat. No.EK12F882

Product TypeAnimal Immunoassay Kits

Size 96T

Product Overview

BioVenic Equine Glucagon Like Peptide 1 (GLP1) ELISA Kit-Competitive is designed for the quantitative determination of Equine Glucagon Like Peptide 1 (GLP1) in serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids using a Competitive ELISA method. For research use only.

Specifications

Assay Type ELISA-Competitive
Specificity The assay kit is specific for Equine GLP1.
Target Species Equine
Species Reactivity Equine
Detection Range 62.5-4000 pg/mL
Sensitivity 23.85 pg/mL
Recovery 80%-102%
Reproducibility Intra-Assay: CV < 10%; Inter-Assay: CV < 10%
Assay Time Around 150 min
Sample Requirement Serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids.

Target Information

Circulating concentrations of the incretin hormone, glucagon-like peptide-1 (GLP-1) correlate with an increased insulin response to carbohydrate intake in animals with Equine metabolic syndrome (EMS). Circulating concentrations of the principal incretin hormone, GLP-1, are lower in horses, than humans, as is their capacity to supplement post-prandial insulin secretion. Research has shown that active GLP-1 is increased in insulin-dysregulated ponies, compared to normal ponies, and likely plays a role in metabolic dysfunction.

Target/Biomarker Equine GLP1
Target Synonym Glucagon Like Peptide 1; GLP-1; glucagon-like peptide-1

Shipping and Storage

This product is shipped with gel ice packs. It is recommended to store at 2-8 °C (Up to 6 months).

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

  1. Kheder, M. H. et al. Equine glucagon-like peptide-1 receptor physiology. PeerJ. 2018, 6: e4316. DOI: 10.7717/peerj.4316
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