Recombinant Mouse DR6/TNFRSF21 Fc Chimera Protein, CF Summary
Product Specifications
When recombinant human APP770 is coated at 2 μg/mL (100 μL/well), the concentration of Recombinant Mouse DR6/TNFRSF21 Fc Chimera that produces 50% of the optimal binding response is found to be approximately 80-400 ng/mL.
Mouse DR6 (Met1 - His349) Accession # NP_848704 |
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.
6985-DR
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution | Reconstitute at 250 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: DR6/TNFRSF21
Death Receptor 6 (DR6), also known as TNFRSF21 and CD358, is a type I transmembrane protein in the TNF receptor superfamily (1). Mouse DR6 consists of a 308 amino acid (aa) extracellular domain (ECD) with four cysteine-rich motifs, a 21 aa transmembrane segment, and a 285 aa palmityolated cytoplasmic region that contains one death domain (2, 3). Within the ECD, mouse and human DR6 share 82% aa sequence identity. DR6 is expressed as an approximately 110 kDa molecule that carries extensive N-linked and O-linked glycosylation in its extracellular region (3, 4). Among hematopoietic cells, DR6 is expressed on monocytes, resting CD4+ T cells, and pro-, pre-, and naïve B cells (5 - 7). DR6 knockout mice exhibit a Th2-biased immune response characterized by exaggerated Th2 and B cell responsiveness in combination with reduced Th1 cell responsiveness and inflammatory leukocyte infiltration (2, 6 - 8). DR6 knockout mice are resistant to induced airway inflammation and experimental autoimmune encephalitis but more susceptible to severe graft versus host disease (8 - 10). DR6 is also expressed on developing neurons where it can bind a shed 35 kDa N-terminal fragment of APP or a fragment of APLP2 (11, 12). This APP fragment is generated following deprivation of neurotrophic factors, and its binding to DR6 triggers DR6-mediated axonal pruning (11). DR6 is constitutively expressed on some prostate cancer cells and can be induced by TNF-alpha on others (3, 4).
- Benschop, R. et al. (2009) Adv. Exp. Med. Biol. 647:186.
- Zhao, H. et al. (2001) J. Exp. Med. 194:1441.
- Klima, M. et al. (2009) Biochim. Biophys. Acta 1793:1579.
- Kasof, G.M. et al. (2001) Oncogene 20:7965.
- Matesanz-Isabel, J. et al. (2011) Immunol. Lett. 134:104.
- Schmidt, C.S. et al. (2003) J. Exp. Med. 197:51.
- Liu, J. et al. (2001) Immunity 15:23.
- Venkataraman, C. et al. (2006) Immunol. Lett. 106:42.
- Schmidt, C.S. et al. (2005) J. Immunol. 175:2286.
- Liu, J. et al. (2002) J. Immunol. 169:3993.
- Nikolaev, A. et al. (2009) Nature 457:981.
- Kuester, M. et al. (2011) J. Mol. Biol. 409:189.
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