
recomDot EBV IgG
recomDot EBV IgM
Protein microarray with recombinant antigens for the detection of IgG or IgM antibodies against Epstein-Barr Virus (EBV) in human serum and plasma
The Epstein-Barr virus, an ubiquitously occurring herpes virus, can cause the symptoms of infectious mononucleosis (Pfeiffer´s disease) on primary infection. Moreover, as a result of the lifelong persistence of this pathogen,reactivations can occur, especially in immunoincompetent persons.
Due to the diversity of symptoms caused by EBV infection and their correspondence with the symptoms of other diseases, a secure EBV diagnosis is of great relevance for differential diagnostics. One of the main tasks in routine diagnosis is therefore the serological differentiation of a primary infection from a past infection and the exclusion of an EBV infection.
The recomDot EBV is based on recombinant, highly specific, immunodominant and phase-specific EBV antigens, whose reactivities can be detected individually. The protein microarray technique combines the high informative value of the Line immunoassay with easy, automated processing on standard ELISA instruments.
recomDot – Your Intelligent Assistant for Routine Laboratory Work
- Multiplex diagnostics – all immunologically relevant antigens are presented separately
- Convenient handling – exchangeable reagents and identical processing for all recomDot tests
- Absolute reliablility – validation by means of integrated controls
- Full automation possible – can be processed on standard ELISA instruments
- Intuitive and user-friendly software – easy test validation and clear result presentation
- Easy data transfer – array reader with LIMS connectivity
Product advantages
- High diagnostic precision – use of recombinant, phase-specific EBV antigens:
- Reliable differentiation of recent/past infections due to the combination of EBNA-1 and the Mikrogen-specific p18MK
- Reliable detection of acute infections due to the high sensitivity of the early antigens
- CE label: The recomDot EBV tests meet the high standard of the EC directive 98/79/EC on in vitro diagnostic medical devices