Recombinant Rat IL-21R Fc Chimera Protein, CF

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6759-RR-050
R&D Systems Recombinant Proteins and Enzymes
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Recombinant Rat IL-21R Fc Chimera Protein, CF Summary

Product Specifications

Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Endotoxin Level
<0.10 EU per 1 μg of the protein by the LAL method.
Activity
Measured by its ability to inhibit IL-21-dependent enhancement of IFN-gamma secretion in NK-92 human natural killer lymphoma cells. The ED50 for this effect is 0.100-0.600 μg/mL.
Source
Mouse myeloma cell line, NS0-derived rat IL-21R protein
Rat IL-21 R
(Met1-Pro236)
Accession # Q5EBB1
IEGRMDP Mouse IgG2A
(Glu98-Lys330)
N-terminus C-terminus
Accession #
N-terminal Sequence
Analysis
Cys20
Structure / Form
Disulfide-linked homodimer
Predicted Molecular Mass
52.2 kDa (monomer)
SDS-PAGE
70-80 kDa, reducing conditions

Product Datasheets

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6759-RR

Carrier Free

What does CF mean?

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.

What formulation is right for me?

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.

6759-RR

Formulation Lyophilized from a 0.2 μm filtered solution in PBS.
Reconstitution Reconstitute at 100 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.
  • 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.
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Background: IL-21R

IL-21 R (interleukin-21 receptor) is a type I transmembrane glycoprotein that belongs to the class I cytokine receptor family, type 4 subfamily (1 ‑ 5). Complex formation between IL-21 R and the common gamma chain ( gamma c), also used for IL-2, IL-4, IL-7, IL-9, and IL-15 receptors, is required for signaling (6, 7). Rat IL-21 R cDNA encodes a 521 amino acid (aa) precursor that contains a 19 aa signal peptide, a 218 aa extracellular domain (ECD) a 21 aa transmembrane domain and a 263 aa cytoplasmic domain. The ECD shows 4 conserved cysteine residues, a fibronectin type III domain, and a WSXWS motif; the cytoplasmin region possesses a Box1 motif, a kinase domain, and several sites for tyrosine phosphorylation (4, 5). One such site, pY502, mediates STAT binding (1, 2). The rat IL‑21 R ECD shares 70%, 91%, 66%, 63% and 58% aa identity with human, mouse, equine, canine and bovine IL-21 R, respectively. One potential 445 aa isoform is reported that contains an alternative start site at Met77. If expressed, it would lack three of the four conserved ECD cysteines seen in full-length rat IL-21 R (8). IL-21 R is expressed mainly on B cells (highest on mature, activated, follicular and germinal center B cells), NK cells, and activated T cells, but is also found on dendritic cells, alternatively activated macrophages, intestinal lamina propria fibroblasts and epithelial cells, and keratinocytes (1, 3 ‑ 5). Both IL-21 and IL-4 are necessary for efficient B cell IgG1 production and normal germinal center architecture (9). IL-21 engagement of the IL‑21 receptor on B cells induces Blimp-1 (which mediates plasma cell differentiation), and is important for memory responses (1, 10, 11). IL‑21 R engagement on mouse NK cells enhances their cytotoxic activity and IFN-gamma production (4, 12). IL‑21 R engagement on CD8+ T cells aids control of viral infection and tumor growth; IL‑21 R is also necessary for sufficient numbers of regulatory T cells to combat chronic inflammation (1, 13, 14). IL‑21 R expression is often up‑regulated in allergic skin inflammation, systemic lupus erythematosus and diffuse large B cell lymphoma (DLBCL) (1, 2, 15, 16).

References
  1. Leonard, W.J. et al. (2008) J. Leukoc. Biol. 84:348.
  2. Konforte, D. et al. (2009) J. Immunol. 182:1791.
  3. Monteleone, G. et al., 2009, Cytokine Growth Factor Rev. 20:185.
  4. Parrish-Novak, et al. (2000) Nature 408:57.
  5. Ozaki, K. et al. (2000) Proc. Natl. Acad. Sci. USA 97:11439.
  6. Asao, H. et al. (2001) J. Immunol. 167:1.
  7. Habib, T. et al. (2002) Biochemistry 41:8725.
  8. Genbank Accession # EDM17511.
  9. Ozaki, K. et al. (2002) Science 298:1630.
  10. Rankin, A.L. et al. (2011) J. Immunol. 186:667.
  11. King, I.L. et al. (2010) J. Immunol. 185:6138.
  12. Kasaian, M.T. et al. (2002) Immunity 16:559.
  13. Frohlich, A. et al. (2009 Science 324:1576.
  14. Tortola, L. et al. (2010) Blood 116:5200.
  15. Jin, H. et al. (2009) J. Clin. Invest. 119:47.
  16. Sarosiek, K.A. et al. (2010) Blood 115:570.
Long Name
Interleukin 21 Receptor
Entrez Gene IDs
50615 (Human); 60504 (Mouse); 102135042 (Cynomolgus Monkey); 705759 (Rhesus Macaque)
Alternate Names
CD360 antigen; CD360; IL-21 R; IL-21 receptor; IL21R; IL-21R; interleukin 21 receptor; interleukin-21 receptor; MGC10967; NILR; Novel interleukin receptor

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