
Bone metabolism Product details
| Productname |
CICP/PICP MicroVue™ Quidel® |
|
C-terminal Propeptide of Collagen Type-I |
| Cat-No. |
8003 |
|
4818 CICP Control (Serum) Set of 4 x 0.5 ml (4 levels)
Average: 40, 140, 245, 500 ng/ml |
| Range |
1 - 80 ng/ml |
| Sensitivity |
0.2 ng/ml |
| Incubation time |
4 hours |
| Sample volume |
25 µl (dilute 1:12) |
| Sample type |
Serum, Heparin- and EDTA Plasma and cell culture |
| Sample preparation |
Avoid hemolysis of specimens. Keep samples refrigerated at
2-8°C for storage of less than 5 days. For longer storage freeze specimens at -20°C or below. |
| Reference values |
| Gender |
Range (ng/ml) |
| Women |
69 - 147 |
| Men |
76 - 163 |
Reference values from children are available. |
| Species |
Human, rabbit, cynomolgus macaque, porcine |
| Tests |
96 Tests |
| Method |
ELISA |
| Product informations |
- Literature (pdf-File 136 kb) - Kit Instructions (pdf-File 187 kb) - Children reference Values (pdf-File 400 kb) - Cross-reaction all species (pdf-File 71 kb) - Cell culture (pdf-File 93 kb) - Bone & Cartilage Metabolism (pdf-File 2,480 kb)
|
| Intended use |
The CICP Kit provides a quantitative method for the determination of collagen production. Collagen type-I is indicative for the collagen production in vivo. As the primary organic constituent of bone, type-I collagen levels have been linked to bone growth and formation. Elevated levels of CICP have been shown in diseases associated with high levels of bone turnover including Paget’s disease, hyperthyroidism, primary hyperparathyroidism and renal osteodystrophia. Frequently, the marker protein CICP has been used in growth deficient children and children with bone diseases. In addition, when metastases of cancer occur to sites in bone and/or liver, a greater proportion of individuals show elevated CICP levels in comparison to patients with other or without metastases. |
| Keywords product |
CICP/PICP, ELISA, C-terminal propeptide of collagen type-I, Bone formation, Bone growth, Bone remodeling, Bone- and livermetastasis, Paget's disease, Hyperthyreosis, Bone marker, Renal osteodystrophia, primary Hyperparathyroidism |
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