HAMA ELISA
- Regulatory Status
- RUO
- Kit size
- 12 x 8
- Method
- ELISA
- Incubation time
- 1 x 1 h, 1 x 30 min, 1 x 20 min
- Standard range
- 40 - 1,500 ng/mL
- Specimen / Volumes
- 25 µL serum, plasma
- Substrate / isotope
- TMB 450 nm
| instructions for use |
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| instructions for use |
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Clinically, mouse monoclonal antibodies (IgG) and their fragments are used for in-vivo diagnostic procedures (radionuclides) and treatment for patients with various diseases. In patients, even a single dose injection of murine monoclonal IgG may induce immune response directed against this foreign protein (immunogen). In the circulation, the presence of human antibody against murine IgG would bind to the injected murine IgG and, therefore, diminish the efficacy of either in-vivo diagnosis or treatment. Especially, the HAMA would increase the risk of anaphylactic complications to subsequent administration of the murine IgG based therapy.
Distributed by Tecan, IBL International GmbH.
For concrete data please consult the Instruction for Use in the download box on the top right side.
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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