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Recombinant Human DEC-205/CD205 Fc Chimera Protein, CF

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When Recombinant CD302/CLEC13A Fc Chimera (Catalog # 10203-CL) is immobilized at 5 μg/mL, 100 μL/well, Recombinant Human DEC-205/CD205 Fc Chimera (Catalog # 10205-DE) binds with an ED50 of 2.4-24 μg/mL.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Human DEC-205/CD205 Fc Chimera Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Human CD302/CLEC13A Fc Chimera (Catalog # 10203-CL) is immobilized at 5 µg/mL (100 µL/well), Recombinant Human DEC-205/CD205 Fc Chimera (Catalog # 10205-DE) binds with an ED50 of 4-28 μg/mL.
Source
Human embryonic kidney cell, HEK293-derived human DEC-205/CD205 protein
Human DEC-205/CD205
(Ser28-Asp1666)
Accession # O060449.3
IEGRMD Human IgG1
(Pro100-Lys330)
N-terminus C-terminus
Accession #
N-terminal Sequence
Ser28
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
215 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
200-250 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 Human DEC-205/CD205 Fc Chimera Protein, CF

  • CD205
  • CLEC13B
  • C-type lectin domain family 13 member B
  • DEC205
  • DEC-205
  • GP200-MR6
  • Ly75
  • Ly-75
  • Lymphocyte antigen 75

Background

DEC-205, also known as CD205 and lymphocyte antigen 75 (Ly75), is a type I transmembrane protein that is part of the macrophage mannose receptor (MMR) family of C-type lectins (1). Both the human and mouse proteins share a similar extracellular (ECD) structure consisting of a cysteine rich N-terminal domain, a fibronectin type II domain, and multiple C-type lectin-like domains (1, 2). The mature ECD of human DEC-205 shares 68% amino acid (aa) identity with mouse DEC‑205. DEC‑205 is primarily expressed on dendritic cells (DC) of lymphoid tissues and at lower levels on macrophages and T cells (3, 4). DEC-205 functions as an endocytic receptor for antigens (3, 4). DEC-205 was shown to be a a cell surface receptor for CpG-oligonucleotides (ODN), as mice deficient in DEC-205 have impaired DC and B-cell maturation (5). DEC-205 expressing Kupffer stellate macrophage cells in the liver responded to CpG-ODN and subsequently released cytokines to promote NKT cell activation, leading to liver damage (6). DEC-205 also recognizes apoptotic and necrotic cells by binding to keratin in a pH-dependent fashion, leading to either immune activation or tolerance in the absence or presence of inflammatory stimuli (7, 8). DEC-205 positive macrophages in the human gastric mucosa were shown to mediate local and systemic immune responses to H. pylori infection, which affects systemic immunity (9). DEC-205 was also found to exist as an intergenic splice variant able to form a fusion protein with CD302 in Hodgkin's lymphoma cell lines (10). The DEC-205/CD302 fusion protein was also found to be expressed by mature dendritic cells which altered endocytic capacity of DEC-205, although the wild-type single gene transcripts were the dominant isoforms expressed (11). DEC-205 has been widely used in immune therapies for vaccine generation. Targeting of antigens to DEC-205 resulted in enhanced antigen presentation by DC. In combination with adjuvants, proteins coupled to antibodies against DEC-205 induced strong pathogen-specific immune responses, while without additional adjuvant tolerance could be induced (12).
  1. Butler, M. et al. (2007) Immunology. 120:362.
  2. Jiang, W. et al. (1995) Nature. 375:151.
  3. Bonifaz, L. et al. (2002) Jour. Exp. Med. 196:1627.
  4. Shrimpton, R. et al. (2009) Mol. Immunol. 46:1229.
  5. Lahoud MH. et al. (2018) Proc Natl Acad Sci U.S.A. 109:16270.
  6. Hou X. et al. (2017) Cell Mol Immunol. 14:675.
  7. Cao L. et al. (2016) Proc Natl Acad Sci U.S.A. 113:13438.
  8. Hawiger D. et al. (2001) J Exp Med. 194:769.
  9. Kita M. et al. (2018) Oncotarget. 9:15828.
  10. Kato, M. et al. (2003) J Biol Chem. 278:34035.
  11. Butler M. et al. (2017) J. Immunol. 120:362.
  12. Niezold T. et al. (2015) Immunology. 145:519.

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