Estriol High Sensitive Saliva ELISA
- Regulatory Status
- RUO
- Kit size
- 12 x 8
- Method
- ELISA
- Incubation time
- 1x2h; 1x30min
- Standard range
- 2 - 288 pg/mL
- Specimen / Volumes
- 100 µL saliva
- Substrate / isotope
- TMB 450 nm
Saliva Testing of hormone levels
Enzyme immunoassay for the quantitative determination of Estriol in human saliva.
It is a product of the metabolism of estrone and estradiol and is excreted in the urine in greater amounts than estradiol.
The new IBL International Estriol high sensitive Saliva ELISA includes harmonized reagents within the IBL Saliva ELISA product line.
Consistent and reliable processing within Saliva product line
Our Saliva ELISA product line (Testosterone, Progesterone, 17ß-Estradiol, Estriol, DHEA) can be processed in a similar way and be easily performed in combination:
Benefits of the Estriol high sensitive Saliva ELISA
- The TMB, washing and stop solutions are harmonized;
- The kits contain as few as 6 standards and 2 controls;
- Only 50 µL (max 100 µL) sample volume are required;
- All kits use the same sample diluent buffer.
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.
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.
Happy to help.
At Tecan, we are driven to improve people’s lives and health.