T3 Total ELISA
- Regulatory Status
- IVD
- Kit size
- 12 x 8
- Method
- ELISA
- Incubation time
- 2 x 30 / 1 x 10 min
- Standard range
- 0 - 10 ng/mL.
- Specimen / Volumes
- 50 µl Serum / Plasma
- Substrate / isotope
- TMB 450 nm
| instructions for use |
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Intended Use
The DRG T3 Total ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of total T3 (triiodothyronine) in serum and plasma.
Summary and Explanation
Measurement of serum triiodothyronine concentration is generally regarded as a valuable tool in the diagnosis of thyroid dysfunction. This importance has provided the impetus for the significant improvement in assay methodology that has occurred in the last two decades. The advent of monospecific antiserum and the discovery of blocking agents to the T3 binding serum proteins has enabled the development of procedurally simple radioimmunoassays [1][2].
For concrete data please consult the Instruction for Use in the download box on the top right side.
- Barker, S.B., "Determination of Protein Bound Iodine." Joumal Biological Chemistry, 173, 175, (1948).
- Chopra, I.J., Solomon, D.H., and Ho, R.S., "A Radioimmunoassay of Triiodothyronine" J. Clinical EndocrinoL, 33, 865 (1971).
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.
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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