Recombinant Feline IL-8/CXCL8 Protein, CF Summary
Details of Functionality |
Measured by its ability to chemoattract BaF3 mouse pro‑B cells transfected with human CXCR2. The ED50 for this effect is 2-10 ng/mL. |
Source |
E. coli-derived feline IL-8/CXCL8 protein Ala23-Ala101 |
Accession # |
|
N-terminal Sequence |
Ala23 |
Protein/Peptide Type |
Recombinant Proteins |
Gene |
CXCL8 |
Purity |
>97%, by SDS-PAGE under reducing conditions and visualized by silver stain. |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
9 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. |
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 Acetonitrile and TFA. |
Purity |
>97%, by SDS-PAGE under reducing conditions and visualized by silver stain. |
Reconstitution Instructions |
Reconstitute at 100 μg/mL in sterile PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Feline IL-8/CXCL8 Protein, CF
Background
Interleukin-8 (IL-8), also known as CXCL8, GCP-1, and NAP-1, is a widely
expressed proinflammatory member of the CXC family of chemokines. Near
its N-terminus, this 8-9 kDa chemokine contains an ELR motif which is
important for its angiogenic properties (1). CXCL8 can associate into a
homodimer or a heterodimer with CXCL4/PF4 (2), and it can also interact
with matrix and cell surface glycosaminoglycans (3). Mature feline CXCL8
shares 87%, 68%, and 78% amino acid (aa) sequence identiity with
canine, human, and porcine CXCL8 (4). There is no CXCL8 gene counterpart
in rodent. N-terminal truncation of CXCL8 by multiple proteases
generates a range of shorter forms (5). The bioactivity of CXCL8 is
regulated by these truncations, by CXCL8 citrullination at Arg5
(N-terminal to the ELR motif) (6), and by the decoy receptor DARC (7).
CXCL8 effects are mediated through CXCR1/IL-8 RA, which is also used by
CXCL6, and through CXCR2/IL-8 RB, which is used by multiple CXC
chemokines (1). These receptors associate into functional homodimers and
heterodimers with each other (8). Through both CXCR1 and CXCR2, CXCL8
promotes neutrophil adhesion to the vascular endothelium and migration
to sites of inflammation (9). It triggers the antimicrobial activation
of neutrophils through CXCR1 (10). CXCL8 also binds to Serpin A1/alpha-1
Antitrypsin, and this prevents CXCL8 interaction with CXCR1 (11). CXCL8
is upregulated in atherosclerotic lesions and other cardiac pathologies
where it exacerbates inflammatory tissue damage (12). In addition, it
induces VEGF expression, vascular endothelial cell proliferation,
angiogenesis, and tumor cell invasiveness (13-16).
- Lazennec, G. and A. Richmond (2010) Trends Mol. Med. 16:133.
- Nesmelova, I.V. et al. (2005) J. Biol. Chem. 280:4948.
- Pichert, A. et al. (2012) Biomatter 2:142.
- Schmid, J. and C. Weissmann (1987) J. Immunol. 139:250.
- Mortier, A. et al. (2008) Pharmacol. Ther. 120:197.
- Proost, P. et al. (2008) J. Exp. Med. 205:2085.
- Neote, K. et al. (1994) Blood 84:44.
- Munoz, L.M. et al. (2009) J. Immunol. 183:7337.
- Gerszten, R.E. et al. (1999) Nature 398:718.
- Jones, S.A. et al. (1996) Proc. Natl. Acad. Sci. USA 93:6682.
- Bergin, D.A. et al. (2010) J. Clin. Invest. 120:4236.
- Apostolakis, S. et al. (2009) Cardiovasc. Res. 84:353.
- Martin, D. et al. (2009) J. Biol. Chem. 284:6038.
- Li, A. et al. (2005) Angiogenesis 8:63.
- Waugh, D.J. and C. Wilson (2008) Clin. Cancer Res. 14:6735.
- Fernando, R.I. et al. (2011) Cancer Res. 71:5296.
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