Recombinant Cynomolgus PD-1 Fc Chimera Protein, CF
R&D Systems, part of Bio-Techne | Catalog # 8578-PD
Key Product Details
Source
HEK293
Accession #
Structure / Form
Disulfide-linked homodimer
Conjugate
Unconjugated
Applications
Bioactivity
Product Specifications
Source
Human embryonic kidney cell, HEK293-derived cynomolgus monkey PD-1 protein
Cynomolgus Monkey PD-1 (Leu25-Gln167) Accession # NP_001271065 |
IEGRMD | Human IgG1 (Pro100-Lys330) |
N-terminus | C-terminus |
Purity
>95%, by SDS-PAGE with silver staining.
Endotoxin Level
<0.10 EU per 1 μg of the protein by the LAL method.
N-terminal Sequence Analysis
Leu25
Predicted Molecular Mass
43 kDa (monomer)
SDS-PAGE
57-68 kDa, reducing conditions
Activity
Measured by its binding ability in a functional ELISA.
When Recombinant Human PD-L2/B7-DC Fc Chimera (Catalog # 1224-PL) is coated at 0.25 μg/mL (100 μL/well), the concentration of Recombinant Cynomolgus Monkey PD-1 Fc Chimera that produces 50% optimal binding response is 0.03-0.15 μg/mL.
When Recombinant Human PD-L2/B7-DC Fc Chimera (Catalog # 1224-PL) is coated at 0.25 μg/mL (100 μL/well), the concentration of Recombinant Cynomolgus Monkey PD-1 Fc Chimera that produces 50% optimal binding response is 0.03-0.15 μg/mL.
Reviewed Applications
Read 3 reviews rated 5 using 8578-PD in the following applications:
Formulation, Preparation and Storage
8578-PD
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution |
Reconstitute at 100 μg/mL in PBS.
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Shipping | The product is shipped with polar packs. 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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Background: PD-1
PD-L1 expression is constitutive on the same cells and also on nonhematopoietic cells such as lung endothelial cells and hepatocytes (8, 9). Ligation of PD-L1 with PD-1 induces co-inhibitory signals on T cells promoting their apoptosis, anergy, and functional exhaustion (10). Thus, the PD-1:PD-L1 interaction is a key regulator of the threshold of immune response and peripheral immune tolerance (11). Finally, blockade of the PD-1: PD-L1 interaction by either antibodies or genetic manipulation accelerates tumor eradication and shows potential for improving cancer immunotherapy (12, 13).
References
- Ishida, Y. et al. (1992) EMBO J. 11:3887.
- Sharpe, A.H. and G. J. Freeman (2002) Nat. Rev. Immunol. 2:116.
- Coyle, A. and J. Gutierrez-Ramos (2001) Nat. Immunol. 2:203.
- Nishimura, H. and T. Honjo (2001) Trends Immunol. 22:265.
- Watanabe, N et al. (2003) Nat. Immunol. 4:670.
- Zhang, X. et al. (2004) Immunity 20:337.
- Lázár-Molnár, E. et al. (2008) Proc. Natl. Acad. Sci. USA 105:10483.
- Nishimura, H et al. (1996) Int. Immunol. 8:773.
- Keir, M.E. et al. (2008) Annu. Rev. Immunol. 26:677.
- Butte, M.J. et al. (2007) Immunity 27:111.
- Okazaki, T. et al. (2013) Nat. Immunol. 14:1212.
- Iwai, Y. et al. (2002) Proc. Natl. Acad. Sci. USA 99: 12293.
- Nogrady, B. (2014) Nature 513:S10.
Long Name
Programmed Death-1
Alternate Names
CD279, PD1, PDCD1, SLEB2
Entrez Gene IDs
Gene Symbol
PDCD1
UniProt
Additional PD-1 Products
Product Documents for Recombinant Cynomolgus PD-1 Fc Chimera Protein, CF
Product Specific Notices for Recombinant Cynomolgus PD-1 Fc Chimera Protein, CF
For research use only
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