25-Hydroxy Vitamin Dˢ EIA
Product Description
The 25-Hydroxy Vitamin DS EIA Assay is intended for the quantitative determination of 25-hydroxyvitamin D [25(OH)D] and other hydroxylated metabolites in human serum and plasma.
- Actionable clinical assessment of vitamin D status provided by measurement of total 25(OH) vitamin D with co-specificity of 25(OH) vitamin D3 and 25(OH) vitamin D2
- Convenient reagent handling with excellent stability combined with ready to use calibrators and controls
- Assures accuracy of patient results through standardisation to the VDSP ID-LC-MS/MS Reference Method Procedure (RMP)
- Reliable test for monitoring vitamin D therapy, regardless of supplementation form
- Confidence in patient results
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Download: CDC Certified Vitamin D Procedures
- Sempos C. et al. Vitamin D status as an international issue: National surveys and the problem of standardization. Scand J Clin Lab Invest Suppl. 2012 Apr; 72(Suppl 243):32-40.
- Holick, MF., et al. “Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline.” The Journal of Clinical Endocrinology & Metabolism 96.7 (2011): 1911-1930.
- Product Code: AC-57SF1
- Number of Tests: 96 wells
- Sample Type: Serum or plasma
- Sample Volume: 25 μL
- Assay Range: 6.5 – 100 ng/mL (16.3 – 250 nmol/L)
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Related Products
| Assays | Certification | Platform | Clinical Area | Portfolio | RUO/IVD |
|---|---|---|---|---|---|
| 1,25-Dihydroxy Vitamin D EIA | CE MarkedFDA Cleared | Vitamin D | Endocrinology | IVD | |
| 1,25 Dihydroxy Vitamin D RIA | CE MarkedFDA Cleared | Vitamin D | Endocrinology | IVD |