Recombinant Human BMP-6, Biotinylated Protein
Recombinant Human BMP-6, Biotinylated Protein Summary
Product Specifications
Gln382-His513
Analysis
Product Datasheets
BT507B/CF (carrier free)
Discontinued Product
BT507B
| Formulation | Lyophilized from a 0.2 μm filtered solution in HCl with BSA as a carrier protein. |
| Reconstitution | Reconstitute at 100 μg/mL in 4 mM HCl. |
| Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
| Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Scientific Data
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When Biotinylated Recombinant Human BMP-6 (Catalog # BT507B) is used at 0.25 µg/mL, it binds Recombinant Human Activin RIA/ALK-2 Fc Chimera (Catalog # 637-AR) with an ED50 of 0.2-1.2 µg/mL.
Reconstitution Calculator
Background: BMP-6
Bone Morphogenetic Protein 6 (BMP-6), also known as Vgr-1, is a member of the BMP subfamily of TGF-beta superfamily proteins. BMPs are involved in a wide range of processes including embryogenesis, tissue morphogenesis, cell differentiation and migration, and tumorigenesis (1). Human BMP-6 is synthesized as a 513 amino acid (aa) precursor protein that is cleaved at the dibasic cleavage site (RxxR) to release the 18 kDa C-terminal mature protein. Biologically active BMP-6 consists of a disulfide-linked homodimer of the mature protein, although it can also form heterodimers with mature BMP-2 (2, 3). Mature human BMP-6 shares 96% and 98% aa sequence identity with mouse and rat BMP-6, respectively. Cellular responses to BMP-6 are mediated by hetero-oligomeric complexes of type I (Activin RIA/ALK-2 and BMPR-IA/ALK-3) and type II (Activin RIIA and BMPR-II) serine/threonine kinase receptors (4, 5). BMP-6 induces the expression of Noggin and is subsequently antagonized by Noggin (6). BMP-6 induces a wide range of cellular responses. It promotes osteoblast differentiation from mesenchymal stem cells (7), chondrocyte maturation (8), Ang II-induced aldosterone production in the adrenal cortex (4), hormone production and responsiveness in ovarian granulosa cells (9), iNOS and TNF-alpha production in macrophages (5), the cell death of B cells (10), and neurite outgrowth (11). BMP-6 expression is induced in astrocytes surrounding sites of brain injury where it functions as a neuroprotectant (11, 12). It enhances tumor progression by promoting local angiogenesis and differentiation of immune tolerizing M2 macrophages (13-15). Through interactions with the BMP coreceptor RGM-C/Hemojuvelin, BMP-6 plays an important role in iron homeostasis by promoting Hepcidin expression and preventing serum iron overload (16). Heterodimers of BMP-2 and BMP-6 show increased potency at inducing osteoblastic calcium deposition, chondrogenesis, and in vivo bone formation compared to either BMP-2 or BMP-6 homodimers (3).
- Bragdon, B. et al. (2010) Cell Signal. 23:609.
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- Haudenschild, D.R. et al. (2004) Cancer Res. 64:8276.
- Lavery, K. et al. (2008) J. Biol. Chem. 283:20948.
- Grimsrud, C.D. et al. (1999) J. Bone Miner. Res. 14:475.
- Shi, J. et al. (2009) Fertil. Steril. 92:1794.
- Kersten, C. et al. (2005) BMC Immunol. 6:9.
- Yabe, T. et al. (2002) J. Neurosci. Res. 68:161.
- Zhang, Z. et al. (2006) Neuroscience 138:47.
- Dai, J. et al. (2005) Cancer Res. 65:8274.
- Kwon, S.J. et al. (2014) Prostate 74:121.
- Lee, J.-H. et al. (2013) Cancer Res. 73:3604.
- Andriopoulos, B. Jr. et al. (2009) Nat. Genet. 41:482.
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