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 Cynomolgus Monkey CD200 R1 Fc Chimera is immobilized at 2 μg/mL, 100 μL/well, the concentration of Recombinant Human CD200 Fc Chimera (Catalog # ) that produces 50% of the optimal binding response is 1.5-9 ng/mL.
Source
Human embryonic kidney cell, HEK293-derived
Human Cynomolgus Monkey CD200 R1
(Ala27-Leu267)
Accession # XP_005548208IEGRMD Human IgG1
(Pro100-Lys330)N-terminus C-terminus Accession #
N-terminal Sequence
AnalysisAla27
Structure / Form
Disulfide-linked homodimer
Predicted Molecular Mass
53 kDa
SDS-PAGE
85-102 kDa, reducing conditions
9357-CD |
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Formulation Lyophilized from a 0.2 μm filtered solution in PBS. | ||
Reconstitution Reconstitute at 1 mg/mL in PBS. | ||
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. | ||
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Data Images
Bioactivity
| When Recombinant Cynomolgus CD200 R1 Fc Chimera (Catalog #9357-CD) is immobilized at 2 μg/mL, 100 μL/well, Recombinant Human CD200Fc Chimera Recombinant Human CD200 Fc Chimera (Catalog # ) binds with an ED50 of 1.5-9 ng/mL. |
Background: CD200 R1
CD200 R1, also known as OX-2 receptor, is a 90 kDa transmembrane protein in the immunoglobulin superfamily. CD200 R1 is important in the regulation of myeloid cell activity (1-3). The cynomolgus CD200 R1 cDNA encodes a 241 aa extracellular domain (ECD) and 61 aa cytoplasmic tail. The ECD is composed of one Ig-like V‑type domain and one Ig-like C2-type domain (4). Within the ECD, cynomolgus CD200 R1 shares 91%, 54%, and 57% aa sequence identity with human, mouse, and rat CD200 R1, respectively. At least two alternate splice isoforms exist that differ in their cytoplasmic domains. CD200 R1 expression is restricted primarily to mast cells, basophils, macrophages, and dendritic cells (5-7), while its ligand, CD200, is widely distributed (8). Disruption of this receptor-ligand system by knockout of the CD200 gene in mice leads to increased macrophage number and activation and predisposition to autoimmune disorders (9). Association of CD200 with CD200 R1 takes place between their respective N-terminal Ig-like domains (10). CD200 R1 propagates inhibitory signals despite its lacking a cytoplasmic ITIM (immunoreceptor tyrosine-based inhibitory motif) (6, 7, 11, 12).
References:
Rosenblum, M.D. et al. 2006, J. Dermatol. Sci. 41:165.
Gorczynski, R.M. (2005) Curr. Opin. Invest. Drugs 6:483.
Barclay, A.N. et al. (2002) Trends Immunol. 23:285.
Wright, G.J. et al. (2003) J. Immunol. 171:3034.
Shiratori, I. et al. (2005) J. Immunol. 175:4441.
Cherwinski, H.M. et al. (2005) J. Immunol. 174:1348.
Fallarino, F. et al. (2004) J. Immunol. 173:3748.
Wright, G.J. et al. (2001) Immunology 102:173.
Hoek, R.M. et al. (2000) Science 290:1768.
Hatherley, D. and A.N. Barclay (2004) Eur. J. Immunol. 34:1688.
Jenmalm, M.C. et al. (2006) J. Immunol. 176:191.
Zhang, S. et al. (2004) J. Immunol. 173:6786.
Long Name:
CD200 Receptor 1
Entrez Gene IDs:
131450 (Human); 57781 (Mouse); 102139962 (Cynomolgus Monkey)
Alternate Names:
CD200 R1; CD200 receptor 1; CD200R1; CD200RMOX2Rcell surface glycoprotein CD200 receptor 1; Cell surface glycoprotein OX2 receptor 1; cell surface glycoprotein receptor CD200; CRTR2; HCRTR2; MOX2 receptor; MOX2R; OX2RCD200 cell surface glycoprotein receptor
