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SS-B/ La Ab ELISA

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Catalog no.RE75241
Regulatory Status
EU: CE
Kit size
12 x 8
Method
ELISA
Incubation time
3 x 30 min
Standard range
0 - 60 U/mL, cut-off 4 U/mL
Specimen / Volumes
10 µL serum, plasma
Substrate / isotope
TMB 450 nm
instructions for usecertificateMSDS

Enzyme immunoassay for the qualitative and quantitative determination of IgG antibodies against SS-B/La in human serum or plasma (EDTA, citrate, heparin). La, the antigen of SS-B/La-autoantibodies, is a 50 kDa phosphoprotein, component of certain ribonucleoprotein (RNP) complexes and involved in RNA metabolism (as transcription termination factor for RNA polymerase III). SS-B/La-antibodies exhibit a high prevalence (40-90%) for the Sjögren-syndrome (SS), an inflammatory autoimmune disorder of the exocrine glands. They are also associated with systemic lupus erythematosus (SLE); especially with some of its variants (e.g. neonatal LE). In this respect, they resemble SS-A/Ro-antibodies. Often, both antibody species occur concomitantly. However, while SS-A/Ro-Ab can be found separately, SS-B/La-Ab almost exclusively occurs together with SS-A/Ro-Ab. Hence, SS-B/La-antibodies exhibit a somewhat lower sensitivity for SS and SLE, as compared to SS-A/Ro-antibodies, but a higher degree of specificity.

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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