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 ED 50
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 |
|
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
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).
- Crowe, P.D. et al. (1994) Science 264:707.
- Force, W.R. et al. (1995) J. Immunol. 155:5280.
- McCarthy, D.D. (2006) Immunol. Res. 35:41.
- Tumanov, A.V. et al. (2007) Curr. Mol. Med. 7:567.
- Boehm, T. et al. (2003) J. Exp. Med. 198:757.
- Wolf, M.J. et al. (2010) Oncogene 29:5006.
- Bista, P. et al. (2010) J. Biol. Chem. 285:12971.
- van de Pavert, S.A. et al. (2010) Nat. Rev. Immunol. 10:664.
- Mouri, Y. et al. (2011) J. Immunol. 186:5047.
- Vondenhoff, M.F. et al. (2009) J. Immunol. 182:5439.
- Haybaeck, J. et al. (2009) Cancer Cell 16:295.
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