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Recombinant Canine PD-L1/B7-H1 Fc Chimera Protein, CF

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When Recombinant Canine PD-1 Fc Chimera (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.
2 μg/lane of Recombinant Canine PD-L1/B7-H1 Fc Chimera (Catalog # 10746-B7) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands ...read more

Product Details

Summary
Reactivity CaSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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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
IEGRMDHuman IgG1
(Pro100-Lys330)
N-terminusC-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
  • Bioactivity
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

  • Avelumab
  • B7-H
  • B7H1
  • B7-H1
  • B7H1PDCD1L1
  • CD274 antigenMGC142294
  • CD274 molecule
  • CD274
  • PDCD1L1
  • PDCD1LG1
  • PDCD1LG1MGC142296
  • PDL1
  • PD-L1
  • PD-L1B7 homolog 1
  • PDL1PDCD1 ligand 1
  • programmed cell death 1 ligand 1
  • Programmed death ligand 1

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).
  1. Greenwald, R.J. et al. (2005) Annual Review of Immunology 23:515.
  2. Collins, Mary et al. (2005) Genome biology 6:223.
  3. Frigola, X. et al. (2011) Clin. Cancer Res. 17:1915.
  4. Daassi, D. et al. (2020) Nat Rev Immunol. 20:209.
  5. Ray, A. et al. (2015) Leukemia. 29:1441.
  6. Zhao, Y. et al. (2018) Oncotarget. 9:14803.
  7. Herold, M. et al. (2015) J. Immunol. 195:3584.
  8. Jiang, Y. et al. (2020) Canc lett. 468:72.

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