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Total Insulin Northern Lights MBeads Assay

Mercodia

A high-throughput tool enabling high specificity results from small sample volumes. Total Insulin Northern Lights MBeads Assay is intended to be used for the measurement of insulin in conditioned media from perifusion experiments or other in vitro cultures from cells derived from human and mouse specimens. The assay allows the analysis of multiple samples simultaneously, decreasing the cost per data point and the amount of sa…

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Oxidized LDL ELISA

Mercodia

Mercodia Oxidized LDL ELISA kit is intended to be used for in vitro quantification of oxidized low-density lipoproteins (oxidized LDL) in human serum or plasma. Mercodia Oxidized LDL ELISA is a unique sandwich ELISA based on the proprietary mouse monoclonal antibody 4E6, which is directed against a conformational epitope in oxidized ApoB-100. Elevated plasma levels of oxidized LDL are associated with higher cardiovascular ris…

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Glucagon ELISA

Mercodia

The Mercodia Glucagon ELISA is a CE/IVD-labelled, highly specific, and sensitive immunoassay for measuring glucagon in plasma and serum. The highly specific monoclonal antibodies used in this assay enable accurate determination of glucagon without significant cross-reactivity to other circulating pro-glucagon-derived peptides.  

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Mouse Insulin ELISA

Mercodia

Mercodia Mouse Insulin ELISA is an easy-to-use assay based on highly specific monoclonal antibodies with insignificant or no cross-reactivity to C-peptide or proinsulin. A highly specific assay for the quantitative determination of insulin in mouse serum or plasma.  

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Total GLP-1 NL-ELISA

Mercodia

Mercodia Total GLP-1 NL-ELISA provides a chemiluminescent method for the quantitative determination of amidated GLP-1 (1-36) in human serum or plasma samples. The assay has been validated according to CLSI, FDA and EMA guidelines.

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Total GIP NL-ELISA

Mercodia

The Mercodia Total GIP NL-ELISA provides a method for the quantitative determination of GIP in human samples. Mercodia Total GIP NL-ELISA measures active GIP(1-42) to the same extent as its metabolite GIP(3-42). Thus, the rapid degradation of the active GIP(1-42) form is not a problem for the specificity of the assay. Accurate results are obtained even if samples without any stabilizing additives are analyzed.

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