Recombinant Mouse BMPR-IA/ALK-3 Fc Chimera Protein, CF
Recombinant Mouse BMPR-IA/ALK-3 Fc Chimera Protein, CF Summary
Product Specifications
The ED50 for this effect is 0.03‑0.12 μg/mL in the presence of 30 ng/mL of recombinant human BMP-4.
Mouse BMPR-1A/ALK-3 (Met1 - Arg152) Accession # NP_033888 |
IEGRDP | MouseIgG2A (Glu98 - Lys330) |
N-terminus | C-terminus | |
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
7054-MR
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution | Reconstitute at 100 μg/mL in PBS. |
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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Reconstitution Calculator
Background: BMPR-IA/ALK-3
Bone Morphogenetic Protein Receptor IA (BMPR‑IA), also known as ALK‑3, BRK‑1, and CD292, is a glycosylated 60 ‑ 65 kDa type I receptor in the TGF‑ beta serine/threonine kinase receptor family (1 ‑ 3). Binding of TGF‑ beta superfamily ligands induces formation of a heterotetrameric complex that contains two chains each of a type I and a type II receptor in multiple combinations. The type II receptors phosphorylate the type I receptors which then phosphorylate and activate Smad signal transduction proteins (1, 2). Mature mouse BMPR‑IA consisits of a 129 amino acid (aa) extracellular domain (ECD), a 24 aa transmembrane segment, and a 356 aa cytoplasmic region that contains the tyrosine kinase domain (4, 5). Within the ECD, mouse BMPR‑IA shares 98% aa sequence identity with human and rat BMPR‑IA. BMPR‑IA is involved in the development and function of a wide range of tissues. During early embryogenesis it is required for migration of the anterior visceral endoderm (AVE) and proper development of the anterior‑posterior axis (6). Tissue‑specific conditional knockout experiments have demonstrated the importance of BMPR‑IA in the development and morphogenesis of the heart, lung, palate, teeth, and mandible (7 ‑ 9). In the adult, BMPR‑IA plays a role in glucose-stimulated insulin secretion by pancreatic beta cells, osteoclast activity and bone remodeling, reactive astrocyte‑mediated scar formation following spinal cord injury, and ovulation and fertility (10 ‑ 13).
- Wu, M.Y. and C.S. Hill (2009) Dev. Cell 16:329.
- Nickel, J. et al. (2009) Cytokine Growth Factor Rev. 20:367.
- de Caestecker, M. (2004) Cytokine Growth Factor Rev. 15:1.
- Dewulf, N. et al. (1995) Endocrinology 136:2652.
- Koenig, B.B. et al. (1994) Mol. Cell. Biol. 14:5961.
- Miura, S. et al. (2010) Dev. Biol. 341:246.
- Gaussin, V. et al. (2002) Proc. Natl. Acad. Sci. 99:2878.
- Sun, J. et al. (2008) Am. J. Pathol. 172:571.
- Li, L. et al. (2011) Dev. Biol. 349:451.
- Goulley, J. et al. (2007) Cell Metab. 5:207.
- Kamiya, N. et al. (2008) J. Bone Miner. Res. 23:2007.
- Sahni, V. et al. (2010) J. Neurosci. 30:1839.
- Edson, M.A. et al. (2010) Mol. Endocrinol. 24:1251.
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