Recombinant Canine PD-L1/B7-H1 Fc Chimera Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant
Canine PD-1 Fc Chimera
(Catalog #
10553-PD)
is immobilized at 0.5 µg/mL (100
µL/well), Recombinant Canine PD-L1/B7-H1 Fc Chimera (Catalog # 10746-B7) binds
with an ED50 of 0.30-4.50 µg/mL. |
Source |
Human embryonic kidney cell, HEK293-derived canine PD-L1/B7-H1 protein Canine PD-L1/B7-H1 (Phe19-Arg236) Accession # NP_001278901.1 | IEGRMD | Human IgG1 (Pro100-Lys330) | N-terminus | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Phe19 |
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 |
51 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 |
60-80 kDa, under 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 with Trehalose. |
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 Canine PD-L1/B7-H1 Fc Chimera Protein, CF
Background
Programmed
Death Ligand 1 (PD-L1), also known as B7-H1 and CD274, is a transmembrane
glycoprotein in the B7 family of immune regulatory molecules. The B7 family is
comprised of at least 10, structurally related members, and plays a central
role in the regulation of T cell response by eliciting both positive
co-stimulatory and negative inhibitory signals (1). Manipulation of B7 mediated
signaling has shown potential in the treatment of autoimmunity, inflammatory
diseases and cancer (1, 2). Mature PD-L1 consists of 1 IgV-like and 1 IgC-like
region in the extracellular domain (ECD), a transmembrane region and a short
intracellular domain. The ECD of canine PD-L1 shares 80% and 70% amino acid sequence
identity with human and mouse PD-L1, respectively. In humans, alternative
splicing can generate additional isoforms that either lack the first Ig-like
domain or are truncated within the second Ig-like domain (3). PD-L1 binds to T
cell B7-1/CD80 and PD-1 (4). PD-L1 is expressed on inflammatory-activated
immune cells including macrophages, T cells, and B cells, keratinocytes, endothelial
and intestinal epithelial cells, as well as a variety of carcinomas and
melanoma (4). It suppresses T cell activation and proliferation and induces the
apoptosis of activated T cells (5). It plays a role in the development of immune
tolerance by promoting T cell anergy and enhancing regulatory T cell
development (5, 6). PD-L1 favors the development of anti-inflammatory IL-10 and
IL-22 producing dendritic cells and inhibits the development of Th17 cells (5-7).
In cancer, PD-L1 provides resistance to T cell mediated lysis, enhances EMT,
and enhances the tumorigenic function of Th22 cells (8).
- Greenwald, R.J. et al. (2005) Annual Review of Immunology 23:515.
- Collins, Mary et al. (2005) Genome biology 6:223.
- Frigola, X. et al. (2011) Clin. Cancer Res. 17:1915.
- Daassi, D. et al. (2020) Nat Rev Immunol. 20:209.
- Ray, A. et al. (2015) Leukemia. 29:1441.
- Zhao, Y. et al. (2018) Oncotarget. 9:14803.
- Herold, M. et al. (2015) J. Immunol. 195:3584.
- Jiang, Y. et al. (2020) Canc lett. 468:72.
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