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Recombinant Cynomolgus Monkey CD58/LFA-3 Fc Protein, CF

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Measured by its binding ability in a functional ELISA. Recombinant Cynomolgus Monkey CD58/LFA-3 Fc Chimera Protein (Catalog # 11432-CD) binds to recombinant Human CD2 Fc Chimera Protein (1856-CD) with a ED50 of ...read more
2 μg/lane of Recombinant Cynomolgus Monkey CD58/LFA‑3 Fc Chimera Protein (Catalog # 11432-CD) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue ...read more

Product Details

Summary
Reactivity Pm-CmSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Cynomolgus Monkey CD58/LFA-3 Fc Protein, CF Summary

Additional Information
Fc Chimera
Details of Functionality
Measured by its binding ability in a functional ELISA. Recombinant Cynomolgus Monkey CD58/LFA‑3 Fc Chimera (Catalog # 11432-CD) binds to recombinant Human CD2 Fc Chimera Protein (Catalog # 1856-CD) with a ED50 of 0.150-2.00 μg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived cynomolgus monkey CD58/LFA-3 protein
Cynomolgus Monkey CD58
(Ile29-Arg215)
Accession # XP_005542263.1
IEGRMD Human IgG1
(Pro100-Lys330)
N-terminusC-terminus
Accession #
N-terminal Sequence
Ile29
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
48 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
70-78 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 Cynomolgus Monkey CD58/LFA-3 Fc Protein, CF

  • Ag3
  • CD58 antigen
  • CD58 antigen, (lymphocyte function-associated antigen 3)
  • CD58 molecule
  • CD58
  • FLJ23181
  • FLJ43722
  • LFA3
  • LFA-3
  • LFA3ag3
  • lymphocyte function-associated antigen 3
  • Surface glycoprotein LFA-3

Background

T cells require a signal induced by the engagement of the T cell receptor and a "co-stimulatory" signal(s) through distinct T cell surface molecules for optimal T cell expansion and activation. Many cell-bound receptor-ligand pairs have now been shown to be involved in T cell co-stimulation including CD58/CD2 in humans and CD48/CD2 in mice and rats. CD58, also known as lymphocyte function-associated antigen (LFA-3),  belongs to the CD2 family of the immunoglobulin superfamily (1). CD58 is widely expressed on hematopoietic and non-hematopoietic human tissue and has been found on leukocytes, erythrocytes, endothelial cells, epithelial cells and fibroblasts of human origin (2). No mouse or rat homolog of CD58 has as of yet been identified. CD58 has only one known ligand, CD2. CD2 is expressed on T cells, NK cells and dendritic cells (2-4). CD2 ligation by CD58 has been shown to mediate T cell adhesion, T cell activation, T cell cytokine production and T cell and NK cells cytotoxic activity (1, 3, 5, 6). In dendritic cells, CD2 engagement increases MHC Class II, CD40, CD80, CD86, CD58 and CCR7 and induces IL-1 beta and IL-12 cytokine secretion (4). Blockade of CD58-CD2 interaction on NK cells resulted in diminished production of IFN-gamma and TNF-alpha in response to Human cytomegalovirus (HCMV)-infected cells (7). Expression of CD58 was significantly increased in anisomycin-treated hepatocellular carcinoma (HCC), and may be critical player in NK-mediated immunotherapeutic effects (8).
  1. Davis, S.J. and van der Merwe P.A. (1996) Immunol. Today 17:177.
  2. Smith, M.E. and J.A. Thomas (1990) J. Clin. Pathol. 43:893.
  3. Bolhuis, R.L. et al. (1986) J. Immunol. 136:3939.
  4. Crawford, K. et al. (2003) Blood 102:1745.
  5. Kanner, S.B. et al. (1992) J. Immunol. 148:2023.
  6. Bullens, D.M. et al. (2001) International Immunol. 13:181.
  7. Rölle A. et al. (2016) Eur J Immunol. 46:2420
  8. Kim M. et al. (2018) Sci Rep. 8:10668.
 

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