Recombinant Cynomolgus Monkey uPAR Fc Chimera Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Cynomolgus Monkey uPAR Fc Chimera is immobilized at 1.00 ug/mL (100 µL/well), Recombinant Human u-Plasminogen Activator/Urokinase
(Catalog #
1310-SE) binds with an ED 50 of 15.0-90.0 ng/mL. |
Source |
Human embryonic kidney cell, HEK293-derived cynomolgus monkey uPAR protein Cynomolgus Monkey UPAR (Leu23-Arg303) Accession # Q9GK78.1 | IEGRMD | Human IgG1 Fc (Pro100-Lys330) | N-terminus | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Leu23 |
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 |
58 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 |
75-85 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 1.00 mg/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 Monkey uPAR Fc Chimera Protein, CF
Background
Urokinase plasminogen activator receptor (uPAR), also
known as CD87, is a cysteine-rich cell surface glycoprotein belonging to the Ly6/uPAR
(LU) superfamily and is involved in the activation of plasminogen to plasmin
(1). Mature uPAR consists of an extracellular domain (ECD) with 3 LU domains
(D1, D2, and D3) similar to Ly‑6 antigens and snake venom alpha -neurotoxins and a
C-terminal glycosyl-phosphatidylinositol (GPI) anchor linked to the last
residue of the third LU domain (1-3). The ECD of mature cynomolgus uPAR shares 95%
amino acid sequence identity with human uPAR. Posttranslational
modification generates several soluble uPAR fragments including uPAR, uPAR
DIIDIII, and uPAR DI in human (1-3). The urokinase-type Plasminogen Activator
(uPA) is one of two activators that converts the extracellular zymogen
plasminogen to plasmin. The binding of uPAR with uPA initiates a proteolytic
cascade resulting in the degradation of extracellular matrix components and stimulates
tissue remodeling (4). The uPAR/uPA interaction also initiates signal
transduction responses resulting in activation of protein tyrosine kinases,
gene expression, cell adhesion, and chemotaxis (4). uPAR can interact with
integrins to suppress normal integrin adhesive function and promote adhesion to
vitronectin through a high affinity vitronectin binding site (5, 6). uPAR
expression is limited in normal human tissue but is highly expressed by diverse
cancer cells and by non-malignant cells that infiltrate cancers and uPAR
expression is associated with poor prognosis and increased risk of metastasis (7).
uPAR
is considered as a biomarker in many inflammatory diseases including cancer,
cardiovascular diseases, chronic kidney diseases and diabetes (6).
- Blasi, F. and Carmeliet, P. (2002) Nat Rev Mol. Cell Biol 3:932.
- Leth, J.M. and Ploug, M. (2021) Front Cell Dev. Biol. 9:732015.
- Behrendt, N. et al. (1996) J Biol. Chem. 271:22885.
- Mahmood, N. et al. (2018) Front. Oncol. 8:24.
- Smith, H. et al. (2010) Nat Rev Mol Cell Biol 11:23.
- Desmedt, S. et al. (2017) Crit. Rev. Clin. Lab. Sci. 54:117.
- Mazar, A.P. (2008) Clin. Cancer Res. 14:5649.
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