• Purity

  >95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie? Blue Staining.

• Endotoxin Level

  <0.10 EU per 1 μg of the protein by the LAL method.  

• Activity

  Measured by its binding ability in a functional ELISA. When Recombinant Human USAG1 (Catalog # ) is immobilized at 1 μg/mL (100 μL/well), the concentration of Recombinant Mouse LRP-6 (Catalog # 2960-LR) that produces 50% of the optimal binding response is approximately 0.1-0.6 μg/mL.

• Source

  E. coli-derived Phe24-Ser206, with an N-terminal Met

• Accession #

• N-terminal Sequence    
  Analysis

  Met

• Predicted Molecular Mass

  21 kDa

• SDS-PAGE

  21 kDa, reducing conditions

Background: USAG1

USAG1, also known as WISE, Ectodin, or SOSTDC1, is a secreted, monomeric 26-32 kDa glycoprotein of the sclerostin family of BMP antagonists. It functions as a BMP and Wnt antagonist during the development of kidney, tooth, and mammary tissues (1-3). Mature mouse USAG1 contains one cystine knot domain and shares 97% and 99.5% aa identity with human and rat USAG1, respectively (2, 3). USAG1 co-localizes with BMP-7 in the developing and adult kidney, particularly in distal tubule epithelial cells (2, 4). It is also found in ectodermal tissues such as tooth ameloblasts, osteoblasts, cells of the dermal papilla, mammary placode epithelium, and uterine lumenal epithelium (1, 2, 5-7). USAG1 binds BMP-2, -4, -6, and -7, sequestering BMPs and preventing their interaction with BMP receptors (1-4, 8). USAG1 also binds to LRP5 and LRP6 and blocks LRP engagement of Wnt (3, 9). USAG1 coordinates BMP, Wnt, FGF, and Shh signals to regulate apoptosis during tooth and bone development (1, 5, 9, 10). Deletion of USAG1 in mice results in supernumerary teeth, nipples, and whiskers as well as increased bone mineral density (5, 6, 8, 9, 11), while concurrent decreased expression of LRP5 and LRP6 restores normal tooth configurations (9). USAG1  ^-/- mice also show decreased susceptibility to kidney injury which is reversed by neutralizing antibody to BMP-7 (4). In a mouse model of Alport syndrome, deletion of USAG1 ameliorates the loss of renal function (10).

• References:

1. Laurikkala, J. et al. (2003) Dev. Biol. 264:91.

2. Yanagita, M. et al. (2004) Biochem. Biophys. Res. Commun. 316:490.

3. Lintern, K.B. et al. (2009) J. Biol. Chem. 284:23159.

4. Yanagita, M. et al. (2006) J. Clin.  Invest. 116:70.

5. Ellies, D.L. et al. (2014) PLoS One 9:e96257.

6. Ahn, Y. et al. (2013) Development 140:583.

7. Maeda, K. et al. (2007) J. Reprod. Dev. 53:931.

8. Murashima-Suginami, A. et al. (2008) Biochem. Biophys. Res. Commun. 369:1012.

9. Ahn, Y. et al. (2010) Development 137:3221.

10. Tanaka, M. et al. (2010) J. Clin. Invest. 120:768.

11. Kassai, Y. et al. (2005) Science 309:2067.

• Long Name:

  Sclerostin Domain Containing Protein 1/Uterine Sensitization-associated Gene 1 Protein

• Entrez Gene IDs:

  25928 (Human); 66042 (Mouse); 266803 (Rat)

• Alternate Names:

  CDA019; cystine-knot containing secreted protein; DKFZp564D206; Ectodermal BMP inhibitor; Ectodin; sclerostin domain containing 1; sclerostin domain-containing protein 1; SOSTDC1; USAG1; USAG-1; USAG1uterine sensitization-associated protein-1; Uterine sensitization-associated gene 1 protein; WISE