Recombinant Mouse BMPR-IA/ALK-3 Fc Chimera Protein Summary
Details of Functionality
Measured by its ability to inhibit rhBMP-4-induced alkaline phosphatase production by ATDC5 mouse chondrogenic cells. Nakamura, K. et al. (1999) Exp. Cell Res. 250:351. The ED50 for this effect is 0.05-0.2 µg/mL in the presence of 30 ng/mL of recombinant human BMP-4.
Source
Mouse myeloma cell line, NS0-derived mouse BMPR-IA/ALK-3 protein
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Bioactivity
Theoretical MW
41.5 kDa (monomer). Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
55 kDa, reducing conditions
Publications
Read Publications using 437-MR in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS with BSA as a carrier protein.
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Reconstitution Instructions
Reconstitute at 100 μg/mL in sterile PBS containing at least 0.1% human or bovine serum albumin.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse BMPR-IA/ALK-3 Fc Chimera Protein
ACVRLK310q23del
ALK-3
ALK3EC 2.7.11.30
BMP type-1A receptor
BMPR1A
BMPR-1A
BMPRIA
BMPR-IA
bone morphogenetic protein receptor type-1A
bone morphogenetic protein receptor, type IA
CD292 antigen
CD292
EC 2.7.11
Serine/threonine-protein kinase receptor R5
SKR5
type II-like kinase 3
Background
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).
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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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