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C-Peptide ELISA

Catalog no.30253368
Regulatory Status
IVD
Kit size
12 x 8
Method
ELISA
Incubation time
1 x 1h, 1 x 30 min, 1 x 20 min
Standard range
0.2 – 16 ng/mL
Specimen / Volumes
100 µL serum, plasma, urine
Substrate / isotope
TMB 450 nm
instructions for use

Intended Use:

The DRG C-Peptide ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of C-Peptide in serum, plasma (EDTA, lithium heparin or citrate plasma) and urine.

Summary and Explanation:

Insulin is synthesized in the pancreatic beta cells as a 6000 MW component of an 86 amino acid polypeptide called proinsulin. [1, 2, 3] Proinsulin is subsequently cleaved enzymatically, releasing insulin into the circulation along with a residual 3000 MW fragment called connection ("C") peptide, because it connects A and B chains of insulin within the proinsulin molecule. [1, 2, 3, 4] Human C-Peptide, a 31 amino acid residue 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. [4, 5, 6] 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. [7] 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. [3] Also, relative to an insulin assay, the C-Peptide assay's advantage is its ability to distinguish endogenous from injected insulin. 

Thus, low C-Peptide levels are to be expected when insulin is diminished (as in insulin-dependent diabetes) or suppressed (as a normal response to exogenous insulin), whereas elevated C-Peptide levels may result from the increased β-cell activity observed in insulinomas. [3, 6, 9] 

C-Peptide has also been measured as an additional means for evaluating glucose tolerance and glibenclamide glucose tests. [2, 3, 9, 10] 

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. [9] 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. [11, 12, 13] Recently, these indications have been dramatically expanded to permit evaluation of insulin dependence in maturity onset diabetes mellitus.

*Distributed by Tecan.

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

References:

[1] Ashby, J. and Frier, B.: Circulating C-Peptide: Measurement and Clinical Applications. Annals of Clinical Biochemistry. 1981,18:125

[2] Beischer, W.: Proinsulin and C-Peptide in Humans. Hormones in Normal and Abnormal Human Tissues. Volume 3K, Fotherby and Pal, S., ed. (Berlin: Walter DeGruyter). 1983, 1-43

[3] Beyer, J., Krause V., Cordes V.: C-Peptide: Its Biogenesis, Structure, Determination and Clinical Significance. Giornale Italiano di Chimica Clinica 4 Supp. ,1979, 9:22

[4] Bonger, A. and Garcia-Webb, P.: C-Peptide Measurement: Methods and Clinical Utility. CRC Critical Reviews in Clinical Laboratory Sciences. 1984, 19:297

[5] Blix, P. Boddie-Wills, C., Landau, R., Rochman, H. Rubenstein, A.: Urinary C-Peptide: An Indicator of Beta-Cell Secretion under Different Metabolic Conditions. Journal of Clinical Endocrinology and Metabolism. 1982, 54:574,

[6] Rendell, M.: C-Peptide Levels as a Criterion in Treatment of Maturity-Onset Diabetes. Journal of Clinical Endocrinology and Metabolism. 198357 (6): 1198

[7] Horwitz, D., et al.: Proinsulin, Insulin and C-Peptide concentrations in Human Portal and Peripheral Blood. Journal of Clinical Investigation. 1975, 55:1278

[9] Rendell, M.: The Expanding Clinical Use of C-Peptide, Radioimmunoassay. Acta Diabetologica Latina. 1983, 20:105

[10]Heding, L. and Rasmussen, S.: Human C-Peptide in Normal and Diabetic Subjects. Diabetologica. 1975, 11:201,

[11] Canivet, B., Harter, M., Viot, G., Balgrac, N., Krebs, B.: Residual ß-Cell Function in Insulin-Dependent Diabetes: Evaluation by Circadian Determination of C-Peptide Immuno reactivity. Journal of Endocrinological Investigation. 1980, 3:107,

[12] Starr, J., Horwitz, D., Rubenstein, A., Mako, M.: Insulin, Proinsulin and C-Peptide. Methods of Hormone Radioimmunoassay 2nd Ed., Academic Press Inc., 1979.

[13] Rubenstein, A., Kuruya, H., Horwitz, D.: Clinical Significance of Circulating C-Peptide in Diabetes Mellitus and Hypoglycemic Disorders. Archives of Internal Medicine. 1977, 137:625

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