Recombinant Human ST2/IL-33R His-tag Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Human ST2/IL-33R His-tag (Catalog # 11272-ST)
is immobilized at 1 μg/mL (100 µL/well), Recombinant Human IL-33 (Catalog #
3625-IL) binds with an ED 50 of 10.0-80.0 ng/mL. |
Source |
Human embryonic kidney cell, HEK293-derived human ST2/IL-33R protein Lys19-Ser328, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Lys19 |
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 |
36 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 |
55-62 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 with Trehalose. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 250 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 ST2/IL-33R His-tag Protein, CF
Background
Serum stimulation-2 (ST2),
also known as Interleukin receptor like-1 (IL1RL1) and T1, is a member of the
Interleukin-1 receptor superfamily family glycoprotein that contributes to Th2
immune responses (1, 2). Human ST2 consists of an extracellular domain
(ECD) with three Ig-like domains, a transmembrane segment, and a cytoplasmic
domain with an intracellular Toll/interleukin-1 receptor (TIR) domain (3, 4). Within
the ECD, human ST2 shares 68% and 64% amino acid sequence identity with mouse
and rat ST2, respectively. Alternate splicing of human ST2 generates a soluble
isoform that lacks the transmembrane and cytoplasmic regions as well as an
isoform that additionally lacks the third Ig‑like domain (4). ST2 is expressed
on the surface of mast cells, activated Th2 cells, macrophages, and cardiac
myocytes (5-8). It binds IL33, a cytokine that is upregulated by inflammation
or mechanical strain in smooth muscle cells, airway epithelia, keratinocytes,
and cardiac fibroblasts (5, 9). IL-33 binding induces the association of ST2
with IL1R AcP, a shared signaling subunit that also associates with IL1RI and
IL1R rp2 (1, 10, 11). In macrophages, ST2 interferes with signaling
from IL1RI and TLR4 by sequestering the adaptor proteins MyD88 and Mal (7). In
addition to its role in promoting mast cell and Th2 dependent inflammation, ST2
activation enhances antigen induced hypernociception and protects from
atherosclerosis and cardiac hypertrophy (5, 12-14). The soluble ST2 isoform is
released by activated Th2 cells and strained cardiac myocytes and is elevated
in the serum in allergic asthma (6, 8, 15). Soluble ST2 functions as a decoy
receptor that blocks IL33 signaling by full-length ST2 (10, 13‑15).
- Barksby, H.E. et al. (2007) Clin. Exp. Immunol. 149:217.
- Gadina, M. and C.A. Jefferies (2007) Science STKE 2007:pe31.
- Tominaga, S. et al. (1992) Biochim. Biophys. Acta. 1171:215.
- Li, H. et al. (2000) Genomics 67:284.
- Schmitz, J. et al. (2005) Immunity 23:479.
- Lecart, S. et al. (2002) Eur. J. Immunol. 32:2979.
- Brint, E.K. et al. (2004) Nat. Immunol. 5:373.
- Weinberg, E.O. et al. (2002) Circulation 106:2961.
- Sanada S. et al. (2007) J. Clin. Invest. 117:1538.
- Palmer, G. et al. (2008) Cytokine 42:358.
- Chackerian, A.A. et al. (2007) J. Immunol. 179:2551.
- Allakhverdi, Z. et al. (2007) J. Immunol. 179:2051.
- Verri, Jr. W.A. et al. (2008) Proc. Natl. Acad. Sci. 105:2723.
- Miller, A.M. et al. (2008) J. Exp. Med. 205:339.
- Hayakawa, H. et al. (2007) J. Biol. Chem. 282:26369.
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