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SLA Ab ELISA

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Catalog no.RE70791
Regulatory Status
EU: CE
Kit size
12 x 8
Method
ELISA
Incubation time
3 x 30min.
Standard range
0 - 300 U/ml; cut-off 15 U/ml
Specimen / Volumes
10µL serum
Substrate / isotope
TMB 450 nm
instructions for usecertificateMSDS

SLA-Ab ELISA is a solid phase enzyme immunoassay employing human recombinant SLA/LP for the quantitative and qualitative detection of antibodies against soluble liver antigen (SLA) in human serum. The assay is a tool for the diagnosis of autoimmune hepatitis (AIH). Autoimmune hepatitis (AIH) is a chronic progressive liver disease of unknown origin that responds well to immunosuppressive therapy, but has a poor prognosis if untreated. Early and accurate diagnosis is therefore of great importance. AIH is characterized by histological features of periportal hepatitis in the absense of viral markers, by hypergammaglobulinemia and, in the majority of patients, by the presence smooth-muscle autoantibodies (SMA) or liver-kidney microsomal autoantibodies (LKM). These antiof patients with viral hepatitis and other immune-mediated diseases. In contrast, antibodies to soluble autoimmune hepatitis and are present in 20% of all AIH-patients, many of whom are negative for other autoantibodies. It was shown that anti-SLA and anti-LP are directed against the same antigen and thus are identical. The SLA/LP antigen cloned and sequenced in 2000 is a protein of unknown function, suggested to be an UGA-suppressor tRNA-associated protein. ANA/SMA and anti-SLA positive patients share most clinical, biochemical, histological and prognostic features. Distinction of different subgroups according to autoantibody status is therefore clinically not helpful. However, testing for anti-SLA autoantibodies is very important for the diagnosis of AIH in many patients who are negative for other autoantibodies and may otherwise be misdiagnosed.

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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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.