Fibroblast Growth Factor 23 (C-terminal)
Produktdaten
cFGF23
Sample preparation
Centrifuge freshly collected blood as soon as possible
Store centrifuged samples at -20°C for longer storage.
Samples are stable up to 4 freeze and thaw cycles.
Hemolyzed or lipemic samples may cause erroneous results.
Reference values
Median serum (n=35): 0.8 pmol/l
Median EDTA plasma (n=22): 1.3 pmol/l
Median heparin plasma (n=22): 1.2 pmol/l
Median citrate plasma (n=30): 1.4 pmol/l
Product name | Fibroblast Growth Factor 23 (C-terminal) |
Cat-Nr. | BI-20702 |
Range | 0 – 20 pmol/l |
Sensitivity | 0.1 pmol/l (STD2 0.2 pmol/l) |
Incubation time | over night / 1 h / 30 min |
Sample volume | 50 μl |
Sample type | Serum, EDTA/Heparin/Citrate plasma |
Species | Human |
Tests | 96 |
Method | ELISA |
Intended use
Intended use:
FGF23 (fibroblast growth factor 23) is a member of the fibroblast growth factor family and controls phosphate and vitamin D homeostasis. The full-length protein comprises 251 amino acids including a 24 amino acid signal peptide. The N-terminal FGF homology region of FGF23 is separated from the unique C-terminal region by a proteolytic cleavage site. A proportion of FG23 is proteolytically processed between arginine179 and serine180 to generate N-terminal and C-terminal fragments. Therefore, the major forms of FGF23 present in human circulation are hormonally intact FGF23 and inactive N-terminal and C-terminal fragments. FGF23 binds to FGF receptor 1c (FGFR1c) with its N-terminal region, while the C-terminal region is capable of interacting with the co-receptor αKlotho to confer high-affinity binding to the receptor. FGFR1c and αKlotho are expressed in the distal nephron and the parathyroid gland. Co-receptor independent signaling of FGF23 has been described or other FGFRs, which are expressed in a variety of tissues. The main source of FGF23 are osteocytes in the
bone.
Intended applications:
- Bone diseases
- Cancer
- Cardiovascular diseases
- Endocrine disorders
- Metabolic disorders
- Kidney diseases