Estrone Saliva ELISA
- Regulatory Status
- RUO
- Kit size
- 12x8
- Method
- ELISA
- Incubation time
- 2 x 30 min, 1 x 15 min
- Standard range
- 3 -333 pg/µL
- Specimen / Volumes
- 100 µL saliva
- Substrate / isotope
- TMB 450 nm
Intended use
Enzyme immunoassay for the quantitative measurement of Estrone in saliva.
For research use only. Not for use in diagnostic procedures.
For concrete data please consult the Instruction for Use in the download box on the top right side.
- Resnik R, Killam AP, Battaglia FC et al: The stimulation of uterine blood flow by various estrogens. Endocrinology 94:1192, 1974.
- Fayman C, Winter JSD, Reyes FI. Patterns of gonadotropins and gonadal steroids throughout life. Clin. Obstet. Gynecol. 3: 467-483, 1976.
- Baird DT. Fraser IS. Blood production and ovarian secretion rates of estradiol-17ß and estrone in women throughout the menstrual cycle. J Clin Endocrinol. Metab 38: 1009-1017. 1974
- Lindbert BS, Johansson EDB, Nilsson BA: Plasma levels of non conjugated oestrone, oestradiol-17b and oestriol during uncomplicated pregnancy. Acta Obstet Gynecol Scand 32:21, 1974.
- Drafta D, Schindler AE, Stroe EW, Neacsu E. Age-related changes of plasma steroids in normal adult males. J. Steroid Biochem. 17: 683-687, 1982.
- DeVane GW, Czekala NM, Judd HL, Yen SSC. Circulating gonadotropins, estrogens, and androgens in polycystic ovarian disease. Am J Obstet Gynecol 1975; 121:496.
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.