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|Method & Line||Sample & Target||Product||Package Info||Product||Package Info|
|MicroELISA||Serum||EIAgen TMPA IgM Kit||Tests per Package: 96|
|EIAgen||The EIAgen TMPA IgM Kit is an immunoenzymatic capture method for the qualitative determination of IgM-class antibodies to treponema pallidum in human serum.||Code: 081021D||Package: 1 Microplate|
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The EIAgen TMPA IgM Kit is an immunoenzymatic capture method for the qualitative determination of IgM-class antibodies to treponema pallidum in human serum.
The serological diagnosis of Syphilis is performed by demonstrating the presence of significant levels of specific antibodies for Treponema pallidum in the patient's serum.
The reference method used is the FTA-ABS technique which allows the detection of both IgG and IgM. However, its execution is laborious and the interpretation of the results is not simple; alternative methods have therefore been found to simplify the procedure. ELISA gives completely automated, reproducible and specific results, and for this reason is proposed by many operators. The specific assay of IgM as opposed to IgG is of great importance in the diagnosis of congenital Syphilis.
The test for the assay of Treponema pallidum IgM is based on the principle of the capture of these immunoglobulins and the subsequent identification of those which are specific, making use of their ability to bind an antigen conjugated to peroxidase. The capture is performed using monoclonal antibodies bound to the solid phase (microtiter wells). The antigen is composed of purified recombinant proteins of Treponema Pallidum, labelled with peroxidase (1-6).
The kit contains reagents for 96 tests (code 081021D).
Bring reagents to room temperature before use.
Wash Buffer Conc. 10x
Sample Diluent 10
Number of tests