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-terminus | | C-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 |
|
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
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).
-
Lehmann, J.M. et al. (1989) Proc. Natl. Acad. Sci. U.S.A. 86:9891.
- Schrage, A. et al. (2008) Histochem Cell Biol. 129:441.
- Wang, Z. and Yan X. (2013) Cancer Lett. 330:150.
- Bardin, N. et al. (2006) Inflamm Bowel Dis. 12:16.
- Xing, S. et al. (2014) Am J Pathol. 184:1604.
- Ma, X. et al. (2017) Oncol Lett. 13:1681.
- Colomb, F. et al. (2017) J Biol Chem. 292:8381.
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