Human CMV IgM ELISA Kit (DEIA466)

Regulatory status: For research use only, not for use in diagnostic procedures.

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Species Reactivity
Intended Use
The test is intended for the diagnosis of CMV-caused or CMV-associated diseases suchas infectious mononucleosis (IM), CMV syndrome or organ-associated CMV infection in immunocompromised patients, acute CMV infection in infants and congenital CMV infection in newborns. In complex with other serological tests(TORCH) it can be used for diagnosis of acute CMV infection in pregnant women.
Contents of Kit
1. ELISA break-away strips
2. Negative control serum
3. Calibrator
4. Lyofilizedmixture of CMV specific antigens
5. Proxidase conjugate
6. Wash buffer
7. Dilution buffer (DB)
8. Chromogenic substrate (TMB substrate)
9. Stop solution
Store the kit reagents at 2-8°C. For longer period make aliquots and keep them at -20°C. Avoid repeated thawing and freezing. For more detailed information, please download the following document on our website
Diagnostic sensitivity and specificity of the test was 96.2% and 96%, respectively.


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Lee, KA; Kim, YW; et al. Distinct patterns of C4d immunoreactivity in placentas with villitis of unknown etiology, cytomegaloviral placentitis, and infarct. PLACENTA 34:432-435(2013).
Gaj, Z; Wilczynski, J; et al. Decrease in 3-nitrotyrosine in the amniotic fluid of women with cytomegalovirus infection. JOURNAL OF OBSTETRICS AND GYNAECOLOGY 34:251-254(2014).

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