Recombinant Human IL-31 (HEK293-expressed) Protein, CF Summary
| Details of Functionality |
Recombinant Human IL-31 (HEK293-expressed) (Catalog # 10425-IL) stimulates CCL2/JE/MCP-1
secretion from the BEAS-2B Human lung bronchial epithelial cell line. The ED50
for this effect is <5 ng/mL. |
| Source |
Human embryonic kidney cell, HEK293-derived human IL-31 protein Leu27-Thr164 |
| Accession # |
|
| N-terminal Sequence |
Leu27 |
| 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 |
16 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 |
19-29 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 200 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 Human IL-31 (HEK293-expressed) Protein, CF
Background
Human
Interleukin-31 (IL-31) is a short-chain member of the alpha -helical family
of cytokines. The human IL-31 cDNA encodes a 164 amino acid (aa) precursor that
contains a signal peptide and a mature protein (1, 2). The mature region shows
four alpha -helices which would be expected to show a typical up‑up‑down‑down
topology. Human and mouse IL-31 share 24% aa sequence identity in the mature
region (1). IL-31 is mainly associated with activated T cells and
preferentially expressed by Th2 rather than Th1 cells. IL-31 signals via a
heterodimeric receptor complex composed of a 120 kDa, gp130-related
molecule termed IL‑31 RA (also GPL and GLM-R) and the 180 kDa oncostatin M
receptor (OSM R beta) (2-6). In the complex, IL-31 directly binds to IL-31 RA, not
OSM R (2, 3). IL-31 signaling has been shown to involve the Jak/STAT pathway,
the PI3 kinase/AKT cascade, and the MAP kinase pathway (2-5). STAT3 is an important
factor in MCP-1 (CCL2) regulation in tumor cells, as well as in keratinocytes.
Impaired IL-31-induced production of MCP-1 in MT (mutant IL-31RA-S521F) cells
is, at least in part, attributed to the much‑reduced STAT3 activation in IL-31
signaling (9). Although multiple
isoforms of IL-31 RA are known, only a form that contains the entire length of
the cytoplasmic domain is signaling-capable (2, 3). The IL-31 receptor is
constitutively expressed by keratinocytes and up‑regulated by IFN-gamma on
monocytes (1). Studies using transgenic mice indicate that IL-31 may contribute
to the pruritis (itching) associated with nonatopic dermatitis (1, 7). Eccrine sweat is
secreted onto the skin's surface and is not harmful to normal skin, but can
exacerbate eczematous lesions in atopic dermatitis. IL-31 seems to be a sweat
stimulator that activates keratinocytes to produce inflammatory cytokine CCL2
(10). IL-31 (50 ng/ml) could
significantly activate the release of EGF, VEGF, CCL2 but not IL-6 and IL-8
from BEAS-2B cells after 18 hr (8).
- 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.
- Diveu, 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.
- Takaoka, A. et al. (2005) Eur. J. Pharmacol. 516:180.
- Lam, C. et al. (2007) Immunology. 122:532.
- Shiao, Y. et al. (2013) J. Invest. Derm. 133:5.
- Dai, X. et al. (2013) PLoS One. 8:7.
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