Offline mode

Radio immuno assay for the quantitative determination of blocking autoantibodies against the acetylcholine receptor in human serum. The ARAb Blocking RIA is useful as an aid in the differential diagnosis of myasthenia gravis (MG). Myasthenia gravis (MG) is an acquired disorder of neuromuscular transmission associated with abnormal muscle weakness and fatigabilities on exertion. This muscle weakness increases with muscle activity, eventually reaching a state of pseudoparalysis. After muscle relaxation the motility is restored. Muscles that are required for body posture, including facial and neck muscles as well as ocular muscles and muscles needed for speaking and swallowing are most affected. Clinical symptoms may be restricted to one muscle group, in particular the eye muscles (ocular MG) or become generalized (generalized MG). Myasthenia gravis can occur from early childhood to old age and its prevalence is about 5 per 100,000. In women, the disease usually presents between the ages of 20 to 40, whereas in men the age of presentation tends to be between 40 and 60 years. The incidence of MG is 40 to 60 new cases per million people per year. Autoantibodies directed against acetylcholine receptors along the postsynaptic membrane are responsible for the muscle weakness and fatigabilities in MG. Three functionally different types of antibodies against acetylcholine receptors are detectable in patients with MG: receptor binding, blocking and modulating antibodies. Related to the blocking antibodies there is a significant correlation between the degree of acetylcholine receptor blockade and generalization of muscle weakness. Therefore, measurement of blocking acetylcholine receptor autoantibodies is of additional value in differential diagnosis of MG.

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).

Image on background

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.

Happy to help.

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