Recombinant Rat Lymphotoxin beta R/TNFRSF3 Fc Chimera, CF
Recombinant Rat Lymphotoxin beta R/TNFRSF3 Fc Chimera, CF Summary
Product Specifications
Rat Lymphotoxin beta R (Gln29-Met222) Accession # NP_001008316 |
IEGRMDP | Mouse IgG2a (Glu98-Lys330) |
N-terminus | C-terminus | |
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
8897-LR
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution | Reconstitute at 500 μg/mL in PBS. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Reconstitution Calculator
Background: Lymphotoxin beta R/TNFRSF3
Lymphotoxin beta R (LT beta R; also called TNFRSF3, TNF RIII,or TNF Rrp) is a type I transmembrane glycoprotein within the TNF receptor superfamily (1-3). The rat LT beta R cDNA encodes a 415 amino acid (aa) protein that includes a 30 aa signal peptide, a 191 aa extracellular domain (ECD), a 23 aa transmembrane domain, and a 171 aa cytoplasmic domain. The ECD contains four cysteine-rich motifs characteristic of the TNF receptor superfamily (2). Within the ECD, rat LT beta R shares 90% and 66% aa sequence identity with the ECD of mouse and human LT beta R, respectively. Soluble LT beta R, which can be formed by proteolytic cleavage of the ECD, functions as a decoy receptor for LT beta R ligands and is involved in the suppression of autoimmunity (4, 5). LT beta R is constitutively expressed in cells of myeloid lineage and is upregulated during tissue regeneration (6). It is expressed on mesenchymal stromal organizing cells that give rise to primary, secondary, and tertiary lymphoid structures (7-9). Mice deficient in LT beta R fail to form secondary lymphoid structures (4). LT beta R ligands include homotrimers of LIGHT/TNFSF14 and the heterotrimeric Lymphotoxin alpha 1/ beta 2 (2). Ligand engagement of LT beta R has been shown to induce NF kappa B activation through canonical (IKK) or alternative (NIK/RelB) signaling pathways (5, 10). LT beta R signaling induces production of cytokines (TRANCE/RANK Ligand/TNFSF11, IL-7), chemokines (CXCL8/IL-8, CXCL13/BCL/BCA-1, CCL19/MIP-3 beta, CCL21/6Ckine, CCL2/MCP-1), and adhesion molecules (VCAM-1/CD106, ICAM-1/CD54, MAdCAM) (8, 11). LT beta R is involved in lipid metabolism, atherosclerosis, and intestinal epithelial homeostasis (4, 12, 13). It also regulates cell growth and can initiate inflammation-related carcinogenesis (5, 14).
- Force, W.R. et al. (1995) J. Immunol. 155:5280.
- Remouchamps, C. et al. (2011) Cytokine Growth Factor Rev. 22:301.
- Crowe, P.D. et al. (1994) Science 264:707.
- Tumanov, A.V. et al. (2007) Curr. Mol. Med. 7:567.
- Wolf, M.J. et al. (2010) Oncogene 29:5006.
- Ware, C.F. (2005) Annu. Rev. Immunol. 23:787.
- Boulianne, B. et al. (2012) Front. Immunol. 3:243.
- Mouri, Y. et al. (2011) J. Immunol. 186:5047.
- van de Pavert, S.A. and R.E. Mebius (2010) Nat. Rev. Immunol. 10:664.
- Bista, P. et al. (2010) J. Biol. Chem. 285:12971.
- Mikami, Y. et al. (2014) PLoS One 9:e114791.
- Macho-Fernandez, E. et al. (2015) Mucosal Immunol. 8:403.
- Browning, J.L. (2012) Mucosal Immunol. 5:228.
- Haybaeck, J. et al. (2009) Cancer Cell 16:295.
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