Diabetes & Obesity
Product name |
Intact Proinsulin (TECO®)![]() |
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Cat-Nr. | TE1012 | ||||||||||||
Range | ~ 3 – 100 pmol/l | ||||||||||||
Sensitivity | 0.3 pmol/l | ||||||||||||
Incubation time | 2.5 hours | ||||||||||||
Sample volume | 50 µl | ||||||||||||
Sample type |
Serum, EDTA / Heparin plasma, cell culture |
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Sample preparation |
Fasting blood sample collection. |
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Reference values |
After fasting: mean 3.99 pmol/l +/- 1.58 SD |
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Species |
Human |
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Specificity |
No cross-reactivity has been observed:
* not present in Serum and Plasma samples |
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Tests | 96 tests | ||||||||||||
Method | ELISA | ||||||||||||
Intended use |
Proinsulin is produced in the pancreatic ß-cells and is normally further processed to insulin and C-peptide. It is only seen in low concentrations in the plasma of healthy subjects. An increase in the insulin demand, as provided by insulin resistance in later stages of type 2 diabetes mellitus, can result in increased expression of proinsulin into the blood. Intact proinsulin is rapidly degraded, but is considered to be an independent cardiovascular risk factor. The intact molecule and its degradation products are known to block fibrinolysis because of plasminogen-activator inhibitor (PAI-1) stimulation. In clinical practice, fasting morning intact proinsulin can be used as highly specific indicator of clinically relevant insulin resistance, to serve as the basis for the selection of an insulin resistance therapy, and to monitor the therapeutic effect on ß-cell dysfunction. Patients with type 2 diabetes mellitus and with elevated fasting intact proinsulin levels should be regarded and treated as insulin resistant, in order to reduce the risk for further cardiovascular damage. |
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Product informations |