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Recombinant Mouse sFRP-5 Protein, CF

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Recombinant Mouse sFRP-5 (Catalog # 7195-SF) inhibits Wnt induced TCF reporter activity in HEK293 human embryonic kidney cells. The ED50 for this effect is 0.600-7.20 μg/mL.

Product Details

Summary
Reactivity MuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Mouse sFRP-5 Protein, CF Summary

Details of Functionality
Measured by its ability to inhibit Wnt induced TCF reporter activity in HEK293 human embryonic kidney cells. The ED50 for this effect is 0.600‑7.20 μg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived mouse sFRP-5 protein
Ala22-His314, with an N-terminal HA (YPYDVPDYA) tag
Accession #
N-terminal Sequence
Tyr (N-terminus of Hemagglutinin tag)
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Endotoxin Note
<0.01 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
34.3 kDa.
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
39-42 kDa, reducing conditions
Publications
Read Publications using
7195-SF in the following applications:

Packaging, Storage & Formulations

Storage
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 and NaCl with Trehalose. 
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Reconstitution Instructions
Reconstitute at 200 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Mouse sFRP-5 Protein, CF

  • frizzled-related protein 1b
  • FRP1B
  • FRP-1b
  • SARP3
  • SARP-3
  • secreted apoptosis related protein 3
  • secreted apoptosis-related protein 3
  • secreted frizzled-related protein 5
  • sFRP5
  • sFRP-5

Background

Secreted Frizzled Related Protein‑5 (sFRP‑5), also known as SARP‑3, belongs to a family of Wnt‑binding proteins with homology to the ligand‑binding domain of the Frizzled receptors. sFRPs are approximately 30‑35 kDa in size and contain an N‑terminal Frizzled‑like domain with 10 conserved cysteines and a Netrin‑like C‑terminal domain (1‑3). Mature mouse sFRP‑5 shares 96% and 99% aa sequence identity with human and rat sFRP‑2, respectively (4). During embryonic development, sFRP‑5 is expressed in the anterior visceral endoderm, neural tube, foregut epithelium, and proliferating and prehypertrophic chondrocytes (5‑8). sFRP‑5 activity is required for the development of foregut, liver, ventral pancreas, and somites (6, 7). In the adult, sFRP‑5 is expressed in the retinal pigment epithelium and pancreas (4, 9). sFRP‑5 binds and antagonizes the function of mammalian Wnt‑5a and Wnt‑11 as well as Xenopus Xwnt‑8, resulting in an inhibition of both canonical and non‑canonical Wnt signaling (4, 7, 10). sFRP‑5 down‑regulation is common in breast and gastric cancer cells and is correlated with poor prognosis (11‑13). It functions as a tumor suppressor by inhibiting epithelial‑mesenchymal transition, invasiveness, and tumorigenicity of ovarian cancer cells (14). sFRP‑5 plays an important role in maintaining glucose handling and insulin sensitivity (10). It is secreted by adipocytes and is down‑regulated in mouse models of obesity and type 2 diabetes (10).
  1. Bovolenta, P. et al. (2008) J. Cell Sci. 121:737.
  2. van Amerongen, R. and R. Nusse (2009) Development 136:3205.
  3. Rattner, A. et al. (1997) Proc. Natl. Acad. Sci. 94:2859.
  4. Chang, J. et al. (1999) Hum. Mol. Genet. 8:575.
  5. Leaf, I. et al. (2006) Genesis 44:573.
  6. Satoh, W. et al. (2008) Genesis 46:92.
  7. Li, Y. et al. (2008) Genes Dev. 22:3050.
  8. Witte, F. et al. (2009) Gene Expr. Patterns 9:215.
  9. Melkonyan, H.S. et al. (1997) Proc. Natl. Acad. Sci. 94:13636.
  10. Ouchi, N. et al. (2010) Science 329:454.
  11. Veeck, J. et al. (2008) Carcinogenesis 29:991.
  12. Zhao, C. et al. (2009) BMC Cancer 9:224.
  13. Ho, C.M. et al. (2010) Eur. J. Clin. Invest. 40:310.
  14. Su, H.Y. et al. (2010) Int. J. Cancer 127:555.

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