Name | Anti-Human Osteocalcin (BGP) antibody | |||
Platforms | Chemiluminescence immunoassay (CLIA) Immunofluorescence assay (IFA) |
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Catalog # | K135c2 | K131c1 | ||
Usage | Capture | Detection | ||
Description | Mouse monoclonal antibody, cultured in vitro | |||
Buffer | 1×PBS | |||
Purity | Purity>96%, purified by Protein A/G chromatography | |||
Storage | Aliquot and store at -20°C or lower. Avoid freeze / thaw cycles. |
Name | Osteocalcin (BGP) antigen | |||
Description | Recombinant, C-terminal GST-tagged, in vitro expressed from mammalian cells | |||
Applications | Calibrator and quality control product | |||
Catalog # | C1526 | |||
Purity | >90%, analyzed by R250-stained SDS-PAGE | |||
Buffer | 1×PBS,pH7.4 | |||
Storage | Aliquot and store at -80°C. Avoid freeze / thaw cycles. | |||
SDS-PAGE |
Predicted MW around 35kDa (tagged)
|
1)Maintaining the normal rate of bone mineralization
One of the important functions of BGP is maintaining the normal rate of bone mineralization. After osteocalcin is synthesized, glutamic carboxylation modifications are only carried out at three sites: 17, 21 and 24. When the affinity between carboxylated BGP, free calcium ions and hydroxyapatite (HA) increases, BGP inhibits the abnormal formation of crystal HA and the mineralization rate of cartilages by tightly binding to hydroxyapatite, thus maintaining the normal mineralization rate.
2)Inhibiting the activity of osteoblasts
BGP can also inhibit the activity of osteoblasts by binding to the G-protein coupled BGP receptors expressed on osteoblasts.
3)Regulating bone resorption
BGP regulates bone resorption by recruiting, chemotaxis and activating bone resorbing cells.
A. Osteocalcin (BGP) and primary osteoporosis
The balance of bone formation and bone resorption is broken in patients with osteoporosis, and their serum BGP level has specific changes. The serum BGP level increases despite of the differences in bone formation, resorption and bone turnover rates among postmenopausal women and elderly patients with primary osteoporosis. Higher BGP levels of postmenopausal women indicate the faster loss of bone density and the greater risk of fractures. The BGP level of the elderly decreases gradually with increasing age. However, the BGP level of elderly osteoporosis patients is higher than that of normal elderly people.
Table 1. Clinical reference range of osteocalcin level for osteoporosis
Data Source | Clinical laboratory of Zhongshan hospital affiliated to Fudan University, Shanghai | Clinical laboratory of Shanghai Donghua hospital | ||||
Group | Male | Premenopausal female | Postmenopausal female | Male | Premenopausal female | Postmenopause female |
N-MID BGP Concentration (μg/L) | 6.00~24.66 | 4.11~21.87 | 8.87~29.05 | 13.4±3.6 | 14.8±4.8 | 21.6±4.6 |
Detection Assay | Electrochemiluminescence (ECL) |
Note: The data comes from "WS/T 375-2011 guidelines for clinical application of bone metabolism indicators" Appendix B. Reference range of bone metabolic indicators; N-MID BGP is the N-terminal fragment of osteocalcin, and the BGP molecules are not homogeneous in blood. Intact BGP is unstable in the blood, and is easily cleaved into stable N-MID macromolecular fragments. Intact BGP accounts for 36% of the total BGP, N-MID accounts for 30%, and the rest are other small fragments.
B. Osteocalcin (BGP) and secondary bone diseases
Secondary bone diseases are mostly caused by other diseases such as diabetes, renal diseases, hyperthyreosis, etc. or the use of drugs. The bone metabolism is disordered in such kinds of patients and there are specific changes in their BGP levels. The insulin level decreases in diabetic patients, leading to less interactions between the insulin and the insulin receptors in osteoblasts, thus reducing the promotional effect of insulin-like growth factor 2 (IGF2) on the activity of osteoblasts. The lower activity of osteoblasts, the lower BGP level in serum. Renal function changes in patients with renal osteodystrophy (such as renal insufficiency, renal failure, etc.). The ability of the kidney to clear BGP decreases causing the content of BGP in the blood to increase.
References
[1] Bouillon R, Vanderschueren D, Van HE, et al. Homologous radioimmunoassay of human osteocalcin[J].Clin Chem, 1992, 38(10): 2055-. 2060.
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