Human Oxyntomodulin ELISA Kit | EL-213-15

Cat. No: EL-213-15

$859.99 USD

96 wells

1
Target proteinOxyntomodulin
Alternative nameGCG
Gene ID2641
ReactivityHuman
Detection range7.82-500 ng/mL
Sample typeSerum, plasma and other biological fluids
Sample volume50 µL
Assay time2h 20min
PrecisionIntra-assay CV <8%. Inter-assay CV <10%
ComponentsPre-Coated Microplate - 12 strips x 8 wells (4°C/-20°C)
Standard (Lyophilized) - 2 vials (4°C/-20°C)
Biotinylated-Conjugate (100×) - 60 μL (4°C/-20°C)
Streptavidin-HRP (100×) - 120 μL (4°C/-20°C)
Standard/Sample Diluent Buffer - 20 mL (4°C/-20°C)
Biotinylated-Conjugate Diluent - 10 mL (4°C/-20°C)
HRP Diluent - 12 mL (4°C/-20°C)
Wash Buffer (25×) - 20 mL (4°C/-20°C)
TMB Substrate Solution - 10 mL (4°C/-20°C (store in dark))
Stop Reagent - 6 mL (4°C/-20°C)
Plate Covers - 2 pieces (RT)
Storage4°C/-20°C

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Safety Warning: Research Use Only. Not for diagnostic use.

This kit employs a competitive inhibition immunoassay technique to quantify Oxyntomodulin (OXM) in biological samples.

Introduction

Oxyntomodulin is a 37-residue peptide generated when the proglucagon precursor, encoded by the GCG gene, is cleaved in intestinal L cells; its sequence duplicates the 29 amino acids of glucagon but carries an additional eight-residue extension at the carboxy terminus that distinguishes it from its parent hormone. Released after meals alongside GLP-1, oxyntomodulin acts as a dual agonist at both the glucagon receptor and the GLP-1 receptor, slowing gastric emptying, damping gastric acid output, and blunting appetite. These combined actions on food intake and energy expenditure have made oxyntomodulin and its analogs of interest for weight-management and metabolic research. Because it shares nearly its entire sequence with glucagon, reliable measurement depends on antibodies that recognize its unique C-terminal extension rather than the glucagon core it has in common with other proglucagon-derived peptides.

Principle of the Assay

This kit uses a competitive inhibition enzyme immunoassay format to measure Human Oxyntomodulin (OXM). The microtiter plate is pre-coated with Human OXM, and standards or samples are added to the wells simultaneously with a biotin-conjugated antibody specific to Human OXM. Free OXM present in the standard or sample competes with the plate-bound OXM for this limited supply of biotin-conjugated antibody, meaning that higher concentrations of free OXM result in less antibody binding to the plate. Streptavidin-conjugated Horseradish Peroxidase (HRP) is then added to each well and incubated, linking enzymatic activity to the plate-bound antibody. TMB substrate solution is subsequently added to produce a colorimetric signal, and the reaction is terminated by the addition of a sulphuric acid stop solution. Absorbance is measured spectrophotometrically at 450 nm (± 10 nm). Because signal is inversely proportional to analyte concentration, OXM levels in unknown samples are determined by comparing sample optical density values against the standard curve.