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Get rid of inaccurate calculations - The only direct measurement of free 25-OH Vitamin D by ELISA

Summary

About 90% of the total circulating 25-OH Vitamin D is bound to the so-called VDBP or DBP. The remaining 10% are bound to albumin, the main protein of human blood plasma.

A tiny fraction representing 0.04% of the total 25-OH Vitamin D concentration circulates as a free form. This fraction of free 25-OH Vitamin D relates to the biological activity of Vitamin D, and therefore may better reflect the physiological action of Vitamin D than the total concentration of 25-OH Vitamin D.

Intended use

The Free 25-OH Vitamin D ELISA is a quantitative immunoassay for in vitro determination of the concentration of free 25-OH Vitamin D in human Serum.

Simple, accurate and direct

Why you should use the Free 25-OH Vitamin D ELISA. Following methods for measuring free 25-OH Vitamin D exist:

  1. Centrifugal ultrafiltration – accurate but long and tedious
  2. Calculations – requires three assays and can be inaccurate
  3. Direct measurement by ELISA – simple and accurate

The Free 25-OH Vitamin D Elisa is based on the use of proprietary anti-25-OH D2/D3 monoclonal antibody and offers a direct method for measuring free 25-OH Vitamin D in human serum samples. Clinical studies have been indicating that the measurement of free 25-OH Vitamin D in serum samples of e.g.,

  • pregnant women
  • haemodialysis patients
  • CDK-patients and
  • patients with liver failure
    • provides more relevant diagnostic information than measurement of routine Total 25-OH Vitamin D assays.

      Distributed by TECAN, IBL International

For concrete data please consult the Instruction for Use in the download box on the top right side.

  1. McWhorter, C. A., Mead, M. J., Rodgers, M. D., Ebeling, M. D., Shary, J. R., Gregoski, M. J., Newton, D. A., Baatz, J. E., Hollis, B. W., Hewison, M., & Wagner, C. L. (2023).
    Predicting comorbidities of pregnancy: A comparison between total and free 25(OH)D and their associations with parathyroid hormone.
    The Journal of steroid biochemistry and molecular biology, 235, 106420.
    DOI: 10.1016/j.jsbmb.2023.106420
    PubMed ID: 37913892
  2. Sempos, C. T., Lindhout, E., Heureux, N., Hars, M., Parkington, D. A., Dennison, E., Durazo-Arvizu, R., Jones, K. S., & Wise, S. A. (2022).
    Towards harmonization of directly measured free 25-hydroxyvitamin D using an enzyme-linked immunosorbent assay.
    Analytical and bioanalytical chemistry, 414(27), 7793–7803.
    DOI: 10.1007/s00216-022-04313-y
    PubMed ID: 36109397
  3. Tian, M., Zeng, S., Cai, S., Reichetzeder, C., Zhang, X., Yin, C., Kuang, W., Cheng, K., Jiang, Y., Tao, M., Zeng, Y., Lin, G., Li, J., Gong, F., & Hocher, B. (2022).
    25(OH)VitD and human endocrine and functional fertility parameters in women undergoing IVF/ICSI.
    Frontiers in endocrinology, 13, 986848.
    DOI: 10.3389/fendo.2022.986848
    PubMed ID: 36105399
  4. Jonsdottir, G. M., Kvaran, R. B., Skarphedinsdottir, S. J., Karason, S., Krueger, D., Coursin, D. B., Binkley, N., Hoofnagle, A. N., Hogan, K., Sigurdsson, G. H., & Sigurdsson, M. I. (2022).
    Changes in vitamin D metabolites at the time of critical illness and 6 months later-A prospective observational study.
    Acta anaesthesiologica Scandinavica, 66(10), 1202–1210.
    DOI: 10.1111/aas.14137
    PubMed ID: 36054671

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).

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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.

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