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Recombinant Mouse MCAM/CD146 Fc Chimera Protein, CF

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When Recombinant Mouse MCAM/CD146 Fc Chimera (Catalog #9809-MA) is coated at 1 µg/mL (100 µg/mL), Recombinant Mouse Galectin-3 (Catalog # 9039-GA) binds with an ED50 of 0.075‑0.375 μg/mL.

Product Details

Summary
Reactivity MuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

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Recombinant Mouse MCAM/CD146 Fc Chimera Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Mouse MCAM/CD146 Fc Chimera is immobilized at 1 μg/mL, 100 μL/well, the concentration of Recombinant Mouse Galectin-3 (Catalog # 9039-GA) that produces 50% of the optimal binding response is 0.075-0.375 μg/mL.
Source
Mouse myeloma cell line, NS0-derived mouse MCAM/CD146 protein
Mouse MCAM
(Val24-Val563)
Accession # Q8R2Y2-1
IEGRMDP Mouse IgG2a
(Glu98-Lys330)
N-terminusC-terminus
Accession #
N-terminal Sequence
Val24
Structure / Form
Disulfide-linked homodimer
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
87 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
112-129 kDa, reducing conditions

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
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 500 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 MCAM/CD146 Fc Chimera Protein, CF

  • CD146 antigen
  • CD146
  • cell surface glycoprotein MUC18
  • Cell surface glycoprotein P1H12
  • L-Gicerin
  • MCAM
  • melanoma adhesion molecule
  • melanoma cell adhesion moleculeS-endo 1 endothelial-associated antigen
  • Melanoma-associated antigen A32
  • Melanoma-associated antigen MUC18
  • MUC18
  • MUC18Gicerin

Background

Melanoma cell adhesion molecule (MCAM), also known as MUC18 or CD146, is a member of the immunoglobulin superfamily (IgSF), showing close sequence similarity to neural cell adhesion molecules (1). MCAM is a type I transmembrane glycoprotein that consists of a 23 aa signal peptide, a 540 aa extracellular domain (ECD), a 21 aa transmembrane segment and 64 aa cytoplasmic domain. Within the ECD, mouse MCAM shares 74% and 90% amino acid sequence identity with human and rat MCAM, respectively. Expression of MCAM has been detected in endothelial cells throughout the body and it has been shown to be involved in multiple cellular events including adhesion, migration, proliferation and differentiation (2, 3). Additionally, MCAM has been implicated in recruitment of activated T cells to inflammatory sites and is up-regulated in various inflammatory diseases (3, 4). Inhibiting MCAM signaling has been suggested as a potential therapy for diverse diseases including inflammatory bowel disease and ovarian cancer (5, 6). As a cellular adhesion molecule (CAM), MCAM functions as a molecular mediator to facilitate inter-cellular interactions of homotypic or heterotypic cells, or to intervene in interactions of cell-to-extracellular matrix for responding to physiological signal (7). MCAM has also been shown to be the functional ligand for Galectin-3 on endothelial cell surfaces (7).
  1. Lehmann, J.M. et al. (1989) Proc. Natl. Acad. Sci. U.S.A. 86:9891.
  2. Schrage, A. et al. (2008) Histochem Cell Biol. 129:441.
  3. Wang, Z. and Yan X. (2013) Cancer Lett. 330:150.
  4. Bardin, N. et al. (2006) Inflamm Bowel Dis. 12:16.
  5. Xing, S. et al. (2014) Am J Pathol. 184:1604.
  6. Ma, X. et al. (2017) Oncol Lett. 13:1681.
  7. Colomb, F. et al. (2017) J Biol Chem. 292:8381.

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