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Recombinant Cyno Lymphotoxin beta R/TNFRSF3 His Protein, CF

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Recombinant Cynomolgus Monkey Lymphotoxin beta R/TNFRSF3 His-tag Protein (Catalog # 11152-LR) inhibits Recombinant Human Lymphotoxin alpha 1/ beta 2 (8884-LY) induced IL-8 secretion in A375 human melanoma cells. The ...read more
2 μg/lane of Recombinant Cynomolgus Monkey Lymphotoxin beta R/TNFRSF3 His-tag Protein (Catalog # 11152-LR) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by ...read more

Product Details

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

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Recombinant Cyno Lymphotoxin beta R/TNFRSF3 His Protein, CF Summary

Additional Information
Cynomolgus Monkey His-tag
Details of Functionality
Measured by its ability to inhibit Recombinant Human Lymphotoxin alpha 1/ beta 2  (Catalog # 8884-LY) induced IL-8 secretion in A375 human melanoma cells. The ED50 for this effect is 0.125-1.50 μg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived cynomolgus monkey Lymphotoxin beta R/TNFRSF3 protein
Ser28-Met227, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Ser28 & Gln29 & Gln 31
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
26 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
29-41 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 Cyno Lymphotoxin beta R/TNFRSF3 His Protein, CF

  • CD18
  • D12S370
  • ltbetar
  • LT-BETA-R
  • LTBR
  • lymphotoxin B receptor
  • Lymphotoxin beta R
  • lymphotoxin beta receptor (TNFR superfamily, member 3)
  • Lymphotoxin-beta receptor
  • LymphotoxinbR
  • TNF RIII
  • TNF Rrp
  • TNFCRTNF-RIII
  • TNFR superfamily, member 3
  • TNFR2-RP
  • TNFR3
  • TNF-R-III
  • TNFR-RP
  • TNFRSF3
  • TNFRSF3TNFR-III
  • Tumor necrosis factor C receptor
  • Tumor necrosis factor receptor 2-related protein
  • tumor necrosis factor receptor superfamily member 3
  • tumor necrosis factor receptor superfamily, member 3
  • Tumor necrosis factor receptor type III

Background

Lymphotoxin beta receptor (LT beta R), previously called TNF RIII or TNF R‑related protein (TNF Rrp), is a type I transmembrane glycoprotein within the TNF receptor superfamily, designated TNFRSF3 (1‑3). Cynomolgus monkey and rhesus macaque LT beta R cDNA encodes 435 amino acids (aa) including a 30 aa signal peptide, a 197 aa extracellular domain (ECD), a 21 aa transmembrane domain, and a 187 aa cytoplasmic domain. The ECD contains four cysteine‑rich motifs characteristic of the TNF receptor superfamily (1, 2). Within the ECD cynomolgus monkey LTBR shares 65‑75% aa sequence identity with human, mouse, rat, canine, porcine, equine and bovine LT beta R. Soluble LT beta R can be formed by proteolytic cleavage of the ECD, and is an inhibitor of transmembrane LT beta R, as is recombinant LT beta R, which inhibits autoimmunity (3‑6). LT beta R is expressed by visceral, lymphoid, and other stroma, epithelia and myeloid cells, but not lymphocytes (2, 4). LT beta R ligands include homotrimers of LIGHT (TNFSF14; also a ligand for HVEM) and the heterotrimeric lymphotoxin LT alpha 1/ beta 2 (3, 4, 6). Depending on the cell type and expression of TRAF3, activation of LT beta R has been shown to induce canonical (IKK/RelA; pro‑inflammatory) or alternative (NIK/RelB; lymphoid organogenic) NF kappa B activation (6, 7). LT beta R is expressed on mesenchymal stromal organizing cells that give rise to stroma of primary (thymus), secondary (tonsils, lymph nodes and Peyers patches) and tertiary (ectopic inflammatory) lymphoid structures (3‑5, 8‑10). Secondary immune tissues are absent in LT beta R‑deficient mice (3-5). LT beta R engagement induces production of IL‑7, RANK, TRANCE/RANK L, VEGF‑C, adhesion molecules such as VCAM‑1, ICAM‑1 and MAdCAM, and chemokines such as CXCL13, CCL19 and CCL21 (3, 8 ‑ 10). LT beta R is expressed by hepatocytes, is up‑regulated in regeneration, hepatitis and hepatocellular carcinoma, and influences lipid metabolism and atherosclerosis (4, 6, 11). It regulates cell growth and can initiate inflammation‑related carcinogenesis (6, 11).
  1. Crowe, P.D. et al. (1994) Science 264:707.
  2. Force, W.R. et al. (1995) J. Immunol. 155:5280.
  3. McCarthy, D.D. (2006) Immunol. Res. 35:41.
  4. Tumanov, A.V. et al. (2007) Curr. Mol. Med. 7:567.
  5. Boehm, T. et al. (2003) J. Exp. Med. 198:757.
  6. Wolf, M.J. et al. (2010) Oncogene 29:5006.
  7. Bista, P. et al. (2010) J. Biol. Chem. 285:12971.
  8. van de Pavert, S.A. et al. (2010) Nat. Rev. Immunol. 10:664.
  9. Mouri, Y. et al. (2011) J. Immunol. 186:5047.
  10. Vondenhoff, M.F. et al. (2009) J. Immunol. 182:5439.
  11. Haybaeck, J. et al. (2009) Cancer Cell 16:295.

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