CTX-I (CrossLaps®)
Product Description
The IDS-iSYS CTX-I (CrossLaps®) Assay is intended for the quantitative determination of degradation products of C-terminal telopeptides of Type I collagen (CTX-I) in human serum or plasma on the IDS-iSYS Multi-Discipline Automated System.
Results are to be used in conjunction with other clinical and laboratory data to assist the clinician. CTX-I can be used as an indicator of bone resorption status as well as an aid in monitoring bone resorption changes during hormone replacement and bisphosphonate therapies.
- Exceptional sensitivity and reproducible results – meeting clinicians’ needs for monitoring therapy effectiveness, identifying non-adherent and non-responders to therapy
- Excellent correlation to established CTX-I assays – allowing seamless transition between methods
- Combining bone turnover markers with the established IDS-iSYS 25-Hydroxy Vitamin DS and IDS-iSYS Intact PTH tests from a single sample tube – aiding management of osteoporosis and other metabolic bone diseases
- A reference marker for osteoporosis management as indicated by IOF, IFCC and NBHA
- Reduced tube handling – wide variety of sample types supported
- A complete clinical assay panel supporting bone disease management
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- Michelsen J et al. Bone. Reference intervals for serum concentrations of three bone turnover markers for men and women. 2013 Dec;57(2):399-404.
- Vasikaran SD et al. Markers of bone turnover for the prediction of fracture
- Vasikaran SD et al. International Osteoporosis Foundation and International
- Product Code: IS-3000 / IS-3030
- Number of Tests: 100
- Sample Type: Serum, SST, plasma (lithium heparin, sodium heparin, potassium
- Sample Volume: 45 µL (excluding dead volume)
- Assay Range: 0.033 - 6.000 ng/mL
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