Recombinant Cynomolgus/Rhesus IL-6R alpha Fc Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When
Recombinant
Human Cynomolgus Monkey/Rhesus Macaque IL-6R alpha Fc Chimera (Catalog # 10408-SR)
is immobilized at 0.5 µg/mL (100 µL/well), Recombinant Human IL-6
(Catalog #
7270-IL)
binds with an ED 50 of 7.5-45 ng/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived IL-6R alpha protein Cynomolgus Monkey/Rhesus Macaque IL-6R alpha (Leu20-Asp358) Accession # XP_005541720.1 | IEGRMD | Human IgG1 (Pro100-Lys330) | N-terminus | | C-terminus | |
|
Accession # |
|
Structure / Form |
Disulfide-linked homodimer |
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 |
64 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 |
89-101 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 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 Cynomolgus/Rhesus IL-6R alpha Fc Protein, CF
Background
Interleukin
6 (IL-6) is a multifunctional cytokine that exerts its activities by binding to
a high-affinity receptor complex consisting of two membrane glycoproteins: an
80 kDa ligand binding subunit (IL-6R alpha /CD126) and a 130 kDa
nonligand-binding signal-transducing subunit (gp130/CD130) (1-4). The cynomolgus
IL-6R alpha cDNA encodes a precursor type I transmembrane protein of 468 amino
acids (aa), and based on its similarity with human IL-6R alpha it is predicted to contain a 19 aa signal sequence, a 345 aa extracellular ligand
binding domain, a 21 aa transmembrane region, and a 75 aa cytoplasmic segment
(2). The extracellular segment likely contains an Ig-like and a fibronectin-type III
domain, plus a membrane proximal WSXWS motif. In their extracellular regions, Cynomolgus IL-6R alpha shares 97% aa identity with human IL-6R alpha. Unlike gp130 that is expressed
ubiquitously, the cellular distribution of IL-6R alpha is predominantly
limited to hepatocytes and leukocyte subpopulations such as monocytes,
neutrophils, T and B cells. Soluble IL-6R alpha has been found in various body
fluids (5). Two soluble receptor isoforms that arise either from proteolytic
cleavage of the membrane-bound IL-6R alpha, or by alternative mRNA splicing
(reported only in human) have been described (6, 7). Soluble IL-6R alpha binds
IL-6 with an affinity similar to that of the membrane-bound IL-6 R alpha. More
importantly, the soluble IL-6 R alpha /IL-6 complex is capable of interacting
with the membrane-bound gp130 to activate cells that lack an integral membrane
IL-6R alpha. It has been documented that elevated soluble IL-6R is associated
with numerous diseases including arthritic lesions, multiple myeloma and
Crohn's disease (6, 7).
- Yamasaki, K. et al. (1988) Science 241:825.
- Sugita, T. et al. (1990) J. Exp. Med. 171:2001.
- Hibi, M. et al. (1990) Cell 63:1149.
- Saito, M. et al. (1992) J. Immunol. 148:4066.
- Novick, D. et al. (1989) J. Exp. Med. 170:1409.
- Jones, S.A. et al. (2001) FASEB J. 15:43.
- Jones, S.A. and S. Rose-John (2002) Biochim. Biophys. Acta 1592:251.
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