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C-Peptide IRMA

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產(chǎn)品名稱: C-Peptide IRMA
產(chǎn)品型號: DE35100
產(chǎn)品展商: 原裝進口
產(chǎn)品文檔: 無相關(guān)文檔

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C-Peptide IRMA


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C-Peptide IRMA

產(chǎn)品名稱:C-Peptide IRMA
產(chǎn)    地:Demeditec
產(chǎn)品貨號:DE35100
產(chǎn)品規(guī)格:100 Tests
產(chǎn)品說明:
Special remarks:
The C-PEPTIDE [125I] IRMA system provides a direct quantitative determination of C-peptide in human serum and urine. C-peptide can be assayed in the range of 0?30ng/ml (in human serum) and 0-300 ng/ml (in urine) using 50 µl serum samples. Each kit contains materials sufficient for 100 assay tubes permitting the construction of one standard curve and the assay of 42 unknowns in duplicate. Introduction C-peptide (connective peptide) is a polypeptide with a molecular weight of 3600,containing 31 amino acid. It derives from proinsulin produced in pancreatic beta cells. Proinsulin is converted to insulin and C-peptide, which are then secreted into the portal blood in an equimolar quantity. Contrary to insulin, C-peptide is not extracted by the liver, but enters the systemic circulation. In the diagnosis of diabetes, C-peptide is a more reliable indicator of insulin secretion than is the insulin itself. Further­more, the concentration of C-peptide is not affected by inter­ference from insulin antibodies often present in patients receiving insulin therapy. The assessment of residual endo­genous insulin secretion by the measurement of C-peptide is an indispensable tool for the diagnosis and treatment of diabetes mellitus.
Principle of method
The technology uses two high affinity monoclonal antibodies in an immuno- radiometric assay (IRMA) system. The 125I labelled signal-antibody binds to an epitope of the C-peptid molecule, which is different from that recognised by the unlabelled capture-antibody. The two antibodies react simul­taneously with the antigen present in standards or samples which leads to the formation of a capture antibody - antigen - signal antibody complex, also referred to as a “sandwich”. During a 3-hour incubation period with continuous agitation immuno-complex is immobilised on the reactive surface of test tubes. Reaction mixture is then discarded, test tubes are washed exhaustively, and the radioactivity is measured in a gamma counter. The concentration of antigen is directly proportional to the radio­activity measured in test tubes. By constructing a calib­ration curve plotting binding values against a series of standards containing known amount of C-peptid, the unknown concentration of C-peptid in patient samples can determined.
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