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In Europe, FSME (Tick-borne Encephalitis referred to as TBE) and Lyme Disease (Borreliosis) are the most frequent tick-borne infections. Borreliosis is very widespread but TBE is confined to special endemic regions (in Southern Germany, Thuringia, Austria, Switzerland, Hungary, Sweden, Czech, Slovak Republics, Croatia, Slovenia as well as some regions of former Soviet Union, etc.). Both infections are similar in their development, consisting of two or more phases. The viraemic phase of TBE has an incubation period of 3-14 days with influenza-like symptoms in the first phase (1-8 days). After a non-febrile interval of about one week the infection may enter into a second phase, characterized by neurological symptoms of varying intensity. This stage may last for many weeks. At the beginning of the second sickness phase, usually anti-TBE-IgM antibodies are detectable. Antibody levels reach their peak after 2-6 weeks. It can take 10 months for antibodies to fall below the level of detection. Anti-TBE-IgG antibodies are detectable simultaneously or a few days after the appearance of IgM-antibodies. Infection means immunity which mostly lasts a lifetime. Vaccination will also prevent the disease. Regular serological checks establish whether boosters are required ('vaccination management'). TBE-specific antibodies in Cerebrospinal Fluid (CSF) may be caused by a dysfunction of the hemato-encephalic barrier before or during an immune response to TBE antigens or may be the result of a local immune response. The antibody level fluctuations in the CSF may differ from those prevalent in serum/plasma. With TBE IgM and TBE IgG it is possible to differentiate between specific TBE antibodies of the IgG and the IgM classes. Rheumatic factors and specific IgG do not interfere with IgM determination due to the addition of the RF/IgG-Absorbent. The combination of both test systems allows the determination of the humoral immune status following TBE-vaccination or infection (IgG), early diagnosis of primary infection with TBE (IgM) and monitoring of changes of antibody levels (IgM/IgG) in human serum, plasma and cerebrospinal fluid.

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Our Product Families

Our comprehensive immunoassay portfolio includes a number of specialty diagnostic immunoassays for endocrinology, immunology and autoimmunity, as well as for diagnosis of multiple infectious diseases. We are pioneers and market leaders in saliva diagnostics, with over 40 years of experience supplying a broad portfolio of luminescence- and ELISA-based tests, including our highly acclaimed HMGB1 and MuSK-Ab ELISAs.

And as experts in laboratory automation, we can support our customers with the protocols for open ELISA platforms, such as the Freedom EVOlyzer or Thunderbolt®.

All products are only available for sale to laboratory professionals and may not be available in all countries. Availability and regulatory status may vary across regions depending on local country-specific registration. Please always read and follow the instructions for use. 

All of our assays have been designed and manufactured to meet the highest global regulatory requirements and quality standards. Tecan is certified under ISO 9001:2015, ISO 13485:2016 and is audited by a notified body according to Medical Device Single Audit Program (MDSAP).

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This is who we are.

As part of the Tecan Group, we have a leading market position in diagnostics and research, with over 40 years of experience in the development, manufacture and supply of enzyme-, radiolabel- and luminescence-based immunoassays.

Our range of high-quality immunoassays is supported by a diverse portfolio of automated solutions, making us the perfect partner for you and your customers.

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At Tecan, we are driven to improve people’s lives and health.