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Helicobacter pylori is a 2.5-3 µm long twisted or helical gram-negative germ responsible for 80 90 % of B-gastritis cases and suspected to a major cofactor for the development of gastric and duodenal ulcers. The classical detection methods of Helicobacter pylori like culturing from mucous membrane biopsies or an urease test are only successful in case of a relative high germ count and require an identification directly after the biopsy. Indirect immunofluorescence (IIF) is also used for the detection Helicobacter pylori infection. The colonisation of the gastric and duodenal mucous membranes with Helicobacter pylori can also be detected serologically using an enzyme immunoassay (ELISA) or by performing a Western Blot. Patients with confirmed exposition to Helicobacter pylori often show a positive serological result. Since antibodies persist for a longer time after a Helicobacter pylori infection seropositive individuals are also found in symptom-free patients. The number of seropositive values rises with age. Using the ELISA and the detection of IgA and IgG antibodies against specific proteins of Helicobacter pylori by Western Blotting it is possible to diagnose an acute infection with Helicobacter pylori, even if no germs can be found.

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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.