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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
  • Download: CDC Certified Vitamin D Procedures

    1. 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.
    2. 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.

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25-Hydroxy Vitamin Dˢ EIA


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