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- Antigène Voir toutes C-Peptide Kits ELISA
- C-Peptide
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Reactivité
- Humain
- Méthode de détection
- Colorimetric
- Type de méthode
- Competition ELISA
- Application
- ELISA
- Fonction
- The C-Peptide Elisa Kit is based on the competition principle and the microplate separation. An unknown amount of C-Peptide present in the sample and a fixed amount of C-Peptide Conjugate compete for the binding sites of a polyclonal C-Peptide antiserum coated onto the wells. In a second step an Enzyme Complex binds to C-Peptide Conjugate. The unbound Enzyme Complex is washed off. Having added the Substrate Solution, the concentration of C-Peptide in the samples is inversely proportional to the optical density measured.
- Analytical Method
- Quantitative
- Featured
- Discover our best selling C-Peptide Kit ELISA
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- Discover our top product C-Peptide Kit ELISA
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- Plaque
- Pre-coated
- Restrictions
- For Research Use only
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- Stock
- 4 °C
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Plasma phospholipids, non-esterified plasma polyunsaturated fatty acids and oxylipids are associated with BMI." dans: Prostaglandins, leukotrienes, and essential fatty acids, Vol. 95, pp. 31-40, (2015) (PubMed).
: "Adaptive human CDKAL1 variants underlie hormonal response variations at the enteroinsular axis." dans: PLoS ONE, Vol. 9, Issue 9, pp. e105410, (2014) (PubMed).
: "Cross-sectional analysis of obesity and serum analytes in males identifies sRAGE as a novel biomarker inversely associated with diverticulosis." dans: PLoS ONE, Vol. 9, Issue 4, pp. e95232, (2014) (PubMed).
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Plasma phospholipids, non-esterified plasma polyunsaturated fatty acids and oxylipids are associated with BMI." dans: Prostaglandins, leukotrienes, and essential fatty acids, Vol. 95, pp. 31-40, (2015) (PubMed).
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- Antigène Voir toutes C-Peptide Kits ELISA
- C-Peptide
- Abstract
- C-Peptide Produits
- Synonymes
- insulin 2 Kit ELISA, Ins2 Kit ELISA
- Sujet
- Human C-Peptide has a molecular mass of approximately 3000 daltons. C-Peptide has no metabolic function. However, since C-Peptide and insulin are secreted in equimolar amounts, the immunoassay of C-Peptide permits the quantitation of insulin secretion. This is the reason for the clinical interest of serum and urinary determinations of C-Peptide. Moreover, C-Peptide measurement has several advantages over immunoassays of insulin.The half-life of C-Peptide in the circulation is between two and five times longer than that of insulin. Therefore, C-Peptide levels are a more stable indicator of insulin secretion than the more rapidly changing levels of insulin. A very clear practical advantage of C-Peptide measurement arising from its relative metabolic inertness as compared to insulin is that C-Peptide levels in peripheral venous blood are about 5-6 times greater than insulin levels. Also, relative to an insulin assay, the C-Peptide assay's advantage is its ability to distinguish endogenous from injected insulin. C-Peptide has also been measured as an additional means for evaluating glucose tolerance and glibenclamide glucose tests.C-Peptide levels are in many ways a better measurement of endogenous insulin secretion than peripheral insulin levels. C-Peptide may be measured in either blood or urine. With improved sensitive C-Peptide immunoassays, it is now possible to measure C-Peptide values at extremely low levels. The clinical indications for C-Peptide measurement include diagnosis of insulinoma and differentiation from factitious hypoglycemia, follow-up of pancreatectomy, and evaluation of viability of islet cell transplants. Recently, these indications have been dramatically expanded to permit evaluation of insulin dependence in maturity onset diabetes mellitus.
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