beta2-Glycoprotein I IgM ELISA
- Regulatory Status
- EU: CE
- Kit size
- 12x8
- Method
- ELISA
- Incubation time
- 3x30min
- Standard range
- 0 - 100 U/mL, cut - off 12 U/mL
- Specimen / Volumes
- 10 µL serum, plasma
- Substrate / isotope
- TMB 450 nm
Enzymimmunoassay zur qualitativen und quantitativen Bestimmung von IgM-Antikörpern gegen ß2-Glycoprotein 1 in humanem Serum oder Plasma (EDTA, citrate, heparin).Antikörper gegen Cardiolipin gelten als Klassifikationskriterien des Anti-Phospholipid-Syndroms (APS).Dieses ist durch venöse und arterielle Thrombosen, Thrombozytopenie, Myokardinfarkt, rezidivierendeAborte sowie neurologische Komplikationen charakterisiert. Es kann isoliert als primäres APS auftreten odermit anderen Autoimmunerkrankungen, insbesondere dem Systemischen Lupus Erythematodes (SLE),assoziiert sein (sekundäres APS).Mit einem APS assoziierte Autoantikörper richten sich nicht ausschließlich gegen Cardiolipin und ähnlichePhospholipide, sondern auch gegen Komplexe aus Phospholipiden und Proteinen. ß2-Glycoprotein 1 (ß2-GP1; Apolipoprotein H) wurde als ein derartiges natürliches und essentielles Co-Antigen für Cardiolipin-Autoantikörper identifiziert. Es hat sich gezeigt, dass Antikörper gegen ß2-GP1 mit einem erhöhtenThromboserisiko assoziiert sind. Sie können auch unabhängig von Cardiolipin-Antikörpern vorkommen.
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).
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.