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Recombinant Mouse LRP-5 Protein, CF

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Product Details

Summary
Reactivity MuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Mouse LRP-5 Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. In a Mouse DKK-1 antibody (Catalog # AF1765) coated plate, Recombinant Mouse LRP-5 binds Recombinant Mouse DKK-1 
(Catalog # 5897-DK) with an ED50 of 0.150-1.50 μg/mL.
Source
Human embryonic kidney cell, HEK293-derived mouse LRP-5 protein
Met1-Ser1383, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Ser31
Protein/Peptide Type
Recombinant Proteins
Gene
Lrp5
Purity
>85%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
152.1 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
160 kDa, reducing conditions
Publications
Read Publications using
7344-LR/CF 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.
Purity
>85%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Reconstitution Instructions
Reconstitute at 100 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 LRP-5 Protein, CF

  • BMND1
  • BMND1OPTA1
  • EVR1
  • EVR4
  • HBM
  • low density lipoprotein receptor-related protein 5
  • low density lipoprotein receptor-related protein 7
  • low-density lipoprotein receptor-related protein 5
  • LR3VBCH2
  • LRP5
  • LRP-5
  • LRP7
  • LRP7exudative vitreoretinopathy 1
  • OPPG
  • OPS
  • OPTA1
  • osteoporosis pseudoglioma syndrome
  • VBCH2

Background

The low-density lipoprotein (LDL) receptor-related proteins LRP-5 and LRP-6 (LRP-5/6) constitute a distinct subgroup of the LDL receptor family (1). Both are widely expressed type I transmembrane proteins that function as Wnt co-receptors with Frizzled proteins in the beta -catenin (canonical) signaling pathway. Both also play critical roles in gastrulation and skeletal patterning during development (1-5). The 1614 amino acid (aa) mouse LRP5 contains a 30 aa signal sequence, a 1353 aa extracellular domain (ECD) with four beta -propeller structures, a 23 aa transmembrane domain and a 208 aa cytoplasmic domain (6). The beta -propellers are formed of five LDLR class B domains each, separated by EGF-like motifs, and followed by three cysteine-rich LDLR class A domains (6, 7). The ECD of mouse LRP-5 shares 95%, 99% and 71% aa sequence identity with the ECD of human LRP-5, rat LRP-5, and mouse LRP-6, respectively. LRP-5/6 associates with Wnt/Frizzled complexes, triggering phosphorylation of its intracellular PPPS motifs, binding of Axin, and propagation of beta -catenin signals (1, 7, 8). The LRP-5 ECD can also interact directly with inhibitors, such as Dickkopf (Dkk), Sclerostin, and USAG1/Wise, and the non-Wnt, activating complex of Norrin with Frizzled-4 (2, 7, 9-12). Formation of a ternary complex of LRP-5, Dkk-1, and Kremen triggers the internalization of the complex (1, 2). LRP-5/6 share many, but not all interactions (1, 2). However, deletion of LRP‑6 has a larger effect on embryonic developmental processes, while deletion and polymorphisms of LRP-5 mainly affect bone density (1, 4, 5, 9, 10). In humans, or mouse models, autosomal recessive osteoporosis-pseudoglioma syndrome and hereditary high bone mass (HBM) are caused by loss- and gain-of-function mutations LRP-5, respectively (4, 9, 10, 13). In mice, Wnt/LRP-5 may inhibit duodenal synthesis of the bone antagonist, serotonin, indirectly enhancing bone formation (14). Accordingly, serum serotonin is decreased in human HBM compared to controls (13). 

  1. MacDonald, B.T. et al. (2011) PLoS ONE 6:e23537.
  2. Kikuchi, A. et al. (2007) Cell. Signal. 19:659.
  3. Kelly, O.G. et al. (2004) Development 131:2803.
  4. Joeng, K.S. et al. (2011) Dev. Biol. 359:222.
  5. Holmen, S.L. et al. (2004) J. Bone Miner. Res. 19:2033.
  6. Hey, P.J. et al. (1998) Gene 216:103.
  7. Williams, B.O. and K.L. Insogna (2009) J. Bone Miner. Res. 24:171.
  8. Tamai, K. et al. (2004) Mol. Cell 13:149.
  9. Cui, Y. et al. (2011) Nat. Med. 17:684.
  10. Gong, Y. et al. (2001) Cell 107:513.
  11. Li, X. et al. (2005) J. Biol. Chem. 280:19883.
  12. Semenov, M. et al. (2005) J. Biol. Chem. 280:26770.
  13. Frost, M. et al. (2011) J. Bone Miner. Res. 26:1721.
  14. Yadav, V.K. et al. (2008) Cell 135:825.

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Publications for LRP-5 (7344-LR/CF)(2)

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Bioinformatics

Gene Symbol Lrp5
Uniprot