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This assay can be used to measure Amyloid-β Oligomers that have at least two intact N-termini. Alzheimer's disease (AD) is a neurodegenerative disease, in which Amyloid beta (Aβ) peptides accumulate in the brain and the predominant symptom is a decline of cognitive functions. It has been generally hypothesized that Aβ forms the senile plaques and this denatures the neurons and develops the symptoms of the disease. (This is called the 'amyloid hypothesis'.) However, the 'oligomer hypothesis' is becoming more and more prominent nowadays and it is thought that the disease is developed by decline in cognitive function because these soluble Aβ oligomers, which are intermediate objects of the condensation process, cause strong synaptic injurious effects. It has been reported that when the Aβ oligomers, which are secreted from the cell or are extracted from AD patient's brain, are injected into rat brain, it causes synaptic dysfunction and study memory loss. Moreover, it is also actually observed that the Aβ oligomers are increasing in brains of AD patients compared with healthy individuals.

For concrete data please consult the Instruction for Use in the download box on the top right side.

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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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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