Recombinant Mouse ST2/IL-33R His-tag Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant
Mouse ST2/IL-33R His-tag (Catalog # 10695-MR) is immobilized at 0.5 µg/mL (100
µL/well), Recombinant Mouse IL-33
Recombinant
Mouse IL‑33 (Catalog # 3626-ML) binds with an ED 50
of 0.03-0.27 µg/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived mouse ST2/IL-33R protein Ser27-His331, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Ser27 |
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 |
57-68 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 500 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 ST2/IL-33R His-tag Protein, CF
Background
ST2, also known as IL-1 R4 and T1, is an Interleukin-1 receptor family
glycoprotein that contributes to Th2 immune responses (1, 2). Mouse ST2
consists of a 306 amino acid (aa) extracellular domain (ECD) with three
Ig-like domains, a 23 aa transmembrane segment, and a 212 aa cytoplasmic
domain with an intracellular TIR domain (3). Alternate splicing of the 120 kDa
mouse ST2 generates a soluble 60 kDa isoform that lacks the transmembrane
and cytoplasmic regions (3). Within the ECD, mouse ST2 shares 59% and 81% aa
sequence identity with human and rat ST2, respectively. ST2 is believed to be a useful biomarker for
predicting both acute and chronic heart failure, and is expressed mainly in two
isoforms, as a transmembrane (ST2L) and as a soluble form (sST2) (4,5). ST2L is expressed on the surface of mast cells,
activated Th2 cells, macrophages, and cardiac myocytes (6-9). It binds IL-33, a
cytokine that is upregulated by inflammation or mechanical strain in smooth
muscle cells, airway epithelia, keratinocytes, and cardiac fibroblasts (6, 10).
IL-33 binding induces the association of ST2 with IL-1R AcP, a shared signaling
subunit that also associates with IL-1 RI and IL-1 R rp2 (1, 11, 12). In
macrophages, ST2 interferes with signaling from IL-1 RI and TLR4 by sequestering
the adaptor proteins MyD88 and Mal (8). 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 (6, 13-15). ST2 is released by activated Th2 cells and
strained cardiac myocytes and is elevated in the serum in allergic asthma (7, 9, 16).
Level of ST2 expression is associated
with gastric cancer progression (17). When bound to IL-33, ST2 is indicated as
an immunotherapy target for diagnosis and treament of cancer patients likely to
be resistant to conventional treatments (18). Soluble ST2 functions as a decoy
receptor that blocks IL-33's ability to signal through transmembrane ST2 (11, 14-16).
- Barksby, H.E. et al. (2007) Clin. Exp. Immunol. 149:217.
- Gadina, M. and C.A. Jefferies (2007) Science STKE 2007:pe31.
- Yanagisawa, K. et al. (1993) FEBS Lett. 318:83.
- Pascual-Figal DA et al. (2015) Am J Cardiol 115(7 Suppl):3B-7B.
- Villacorta, Humberto et al. (2016) Arquivos brasileiros de cardiologia vol. 106,2.
- 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.
- Bai, F. et al. (2019) Oncol Lett. 17:5761.
- Kudo-Saito, C. et al. (2020) Cancer Res. 80:1981.
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