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In 2010, the number of dementia patients worldwide was estimated at 36 million. Assuming an ongoing lack of sufficient preventive and curative treatments, this is expected to double every 20 years. Alzheimer’s Disease accounts for roughly 60-70% of all dementia cases. Both prevalence and incidence increase with age. Prevalence is around 1% in those aged 65-69, and more than 30% in those aged 90 or older. The development of the Disease is characterized by three stages, as defined by the US National Institute on Aging workgroups. A preclinical stage of Alzheimer’s Disease, the mild cognitive impairment (MCI) stage due to AD, and the dementia stage due to AD [9-11]. Amyloidosis occurs as early as the preclinical stage. The first cognitive deficits can manifest themselves in MCI stage, while in the dementia stage patients are unable to do any work or daily chores. The concentration of amyloid-beta (1-42) is therefore recognized as a useful biomarker (in combination with other biomarkers such as Tau and Phospho-Tau) in diagnosing Alzheimer’s Disease. Moreover, a number of independent studies (for example [3-5]) showed the ratio of amyloid-beta (1-42) to amyloid-beta (1-40) to be a superior diagnostic marker for Alzheimer’s Disease.

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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.