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Recombinant Cynomolgus/Rhesus SLAM/CD150 His-tag Protein, CF

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Measured by its ability to co-stimulate IL-4 secretion by D10.G4.1 mouse helper T cells in the presence of anti-CD3. The ED50 for this effect is 0.500-2.50 μg/mL.
2 μg/lane of Recombinant Cynomolgus Monkey/Rhesus Macaque SLAM/CD150 His-tag Protein (Catalog # 10971-SL) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® ...read more

Product Details

Summary
Reactivity Pm-Cm, RMSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Cynomolgus/Rhesus SLAM/CD150 His-tag Protein, CF Summary

Details of Functionality
Measured by its ability to co-stimulate IL-4 secretion by D10.G4.1 mouse helper T cells in the presence of anti-CD3. The ED50 for this effect is 0.500-2.50 μg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived SLAM/CD150 protein
Tyr23-Lys236, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Tyr23 & Thr25
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
25 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
42-55 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 250 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/Rhesus SLAM/CD150 His-tag Protein, CF

  • CD 150
  • CD150
  • CD150IPO-3
  • CDw150
  • IPO-3
  • signaling lymphocytic activation molecule family member 1
  • signaling lymphocytic activation molecule
  • SLAM
  • SLAMCD150 antigen
  • SLAMF1

Background

Signaling lymphocytic activation molecule (SLAM), also known as SLAMF1 and CD150, is the founding member of the SLAM subfamily of the CD2 protein family (1, 2). SLAM is a single-pass type I membrane glycoprotein that functions as an adhesion molecule and plays an active role in the regulation of innate and adaptive immunity (1, 2, 4). Mature SLAM consists of an extracellular domain (ECD) containing an Ig-like V-type domain and an Ig-like C2-type domain, a helical transmembrane domain, and a cytoplasmic tail containing 2 immunoreceptor tyrosine-based switch motifs (ITSM) (3, 4). The ECD of cynomolgus SLAM shares 97% amino acid identity with human SLAM. In human, several isoforms resulting from alternative splicing have been identified with functional diversity (4). SLAM is expressed on T cells, B cells, thymocytes, macrophages, dendritic cells, platelets, and hematopoietic stem cells, and it is up-regulated on activated B cells and CD4+ and CD8+ T cells (4-6). SLAM interacts homophilically with low affinity, and this interaction induces a Th0/Th1 phenotype in CD8+ T cells that is characterized by clonal expansion, production of IFN-gamma, and increased cytolytic activity (7, 8). SLAM also plays a role in activation of the PI3K-Akt signaling pathway through its association with the adapter molecule SAP (9). In humans, SLAM functions as a cellular entry receptor for measles virus (10, 11). SLAM deregulation is associated with genomic complexity and independently predicts a worse outcome in chronic lymphocytic leukemia (CLL) (12).
  1. Yurchenko, M. et al. (2018) J. Cell. Biol. 217:1411.
  2. Pellegrini, J. et al. (2021) Autophagy. 17:2629.
  3. Wang, N. et al. (2015) Front. Immunol. 6:158.
  4. Gordiienko, I. (2019) Clinical Immunol. 204:14.
  5. Calpe, S. et al. (2008) Adv Immunol. 97:177.
  6. Wang, N. et al. (2004) J. Exp. Med. 199:1255.
  7. Mavaddat, N. et al. (2000) J. Biol. Chem. 275:28100.
  8. Mehrle, S. et al. (2008) Mol. Immunol. 45:796.
  9. Yurchenko, M.Y. et al. (2005) Exp Oncol. 27:24.
  10. Hsu, E.C. et al. (2001) Virology 279:9.
  11. Gonçalves-Carneiro, D. et al. (2017) J Virol. 91:e02255.
  12. Gian, M.R. et al. (2021) Br. J. Haematol. 192:1068.

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