Recombinant Mouse IL-31 (Mammalian-expressed) Protein, CF Summary
Details of Functionality |
Measured by its ability to induce STAT3 reporter
activity in HEK293 human embryonic kidney cells transfected with mouse IL-31RA
and OSMR beta. The ED50 for this effect is 0.05-0.4 ng/mL. |
Source |
Human embryonic kidney cell, HEK293-derived mouse IL-31 protein Ala31-Cys163 |
Accession # |
|
N-terminal Sequence |
Ala31 |
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 |
15 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 |
16-25 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. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 100 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 Mouse IL-31 (Mammalian-expressed) Protein, CF
Background
Mouse
Interleukin-31 (IL-31) is secreted, short-chain member of
the alpha -helical IL-6 family of cytokines (1, 2). The mouse IL‑31 cDNA
encodes a 163 amino acid (aa) precursor that contains a signal peptide and
a mature protein (3, 4). The mature region shows four alpha ‑helices which
would be expected to generate a typical up-up-down-down topology. Mature mouse IL-31 shares 29% and 63% aa sequence identity with human and rat IL-31, respectively. Neither
mouse nor human IL-31 are active on their counterparts receptors (1). IL-31 is
associated with activated T cells and is preferentially expressed by Th2
rather than Th1 cells (1). IL-31 signals via a heterodimeric receptor complex
composed of a gp130-related molecule termed
IL-31 RA (also GPL and GLM-R) and the 180 kDa oncostatin M receptor
(OSM R beta) (4‑8). In the complex, IL‑31 directly binds to IL‑31 RA,
not OSM R (4, 5). IL-31 signaling has been shown to involve the
Jak/STAT pathway, the PI3 kinase/AKT cascade, and MAP kinase
pathway. Although multiple isoforms of IL-31 RA are known, only a
form that contains the entire length of the cytoplasmic domain is signaling-capable
(4‑7). The IL-31 receptor is constitutively expressed by keratinocytes and
up-regulated by IFN-gamma on monocytes (1, 3). Other cells known to be
responsive to IL-31 include bronchial epithelium, type II alveolar cells,
goblet cells, and likely hematopoietic progenitor cells (9‑11). Functionally,
it has been shown that IL-31 may contribute to clinical pruritis (itching)
associated with nonatopic dermatitis (1, 3, 12). This may be a consequence of
IL-31's ability to induce keratinocyte secretion of multiple cytokines,
including TARC, GRO‑ alpha, MIP‑3 beta and I-309 (1). In addition, IL-31
promotes proliferation of high-density cell populations such as myeloid
progenitor cells, but conversely suppresses proliferation of lung epithelial
cells (1). Finally, IL-31 may actually have a modulating effect on T cell
subsets, influencing the ratio between Th1 and Th2 cells (1).
- Zhang, Q. et al. (2008) Cytokine Growth Factor Rev. 19:347.
- Venereau, E. et al. (2009) J. Biol. Chem. 285:14955.
- Dillon, S.R. et al. (2004) Nat. Immunol. 5:752.
- Diveu, C. et al. (2004) Eur. Cytokine Netw. 15:291.
- Dreuw, A. et al. (2004) J. Biol. Chem. 279:36112.
- Dieu, C. et al. (2003) J. Biol. Chem. 278:49850.
- Ghilardi, N. et al. (2002) J. Biol. Chem. 277:16831.
- Mosley, B. et al. (1996) J. Biol. Chem. 271:32635.
- Chattopadhyay, S. et al. (2007) J. Biol. Chem. 282:3014.
- Perrigoue, J.G. (2009) J. Immunol. 182:6088.
- Broxmeyer, H.E. et al. (2007) Exp. Hematol. 35(Suppl 1):78.
- Takaoka, A. et al. (2005) Eur. J. Pharmacol. 516:180.
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