Recombinant Mouse FGF-17 Protein Summary
Product Specifications
Thr23-Thr216, with an N-terminal Met
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
7400-FG
Formulation | Lyophilized from a 0.2 μm filtered solution in MOPS, (NH4)2SO4, DTT and EDTA with BSA as a carrier protein. |
Reconstitution | Reconstitute at 100 μg/mL in PBS containing at least 0.1% human or bovine serum albumin. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
|
7400-FG/CF
Formulation | Lyophilized from a 0.2 μm filtered solution in MOPS, (NH4)2SO4, DTT and EDTA. |
Reconstitution | Reconstitute at 100 μg/mL in PBS. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
|
Reconstitution Calculator
Background: FGF-17
FGF‑17 is a member of the fibroblast growth factor (FGF) family. FGFs play multiple roles in biological functions, including angiogenesis, mitogenesis, cell differentiation and wound repair. FGFs share 30‑70% amino acid (aa) identity in a conserved, approximately 120 amino acid core domain (1‑3). The mouse or human FGF‑17 cDNA encodes a cleavable 22 aa signal sequence and a 194 secreted mature protein (1). Mature mouse FGF-17 shares 100%, 99%, 99%, 97%, and 97% aa identity with rat, human, porcine, canine and equine FGF‑17, respectively. The FGF domain of FGF‑17 shares the most aa identity with FGF-8 (75%) and FGF-18 (64%). These three FGFs constitute a subfamily that overlaps in some areas of expression and function (1‑5). All are reported to bind and signal through FGF R4 and the “c” splice forms of FGF R1-3 (6, 7). During embryogenesis, FGF‑17 plays an organizing and inducing role in the patterning at the midbrain/hindbrain junction, and is also expressed in hindgut, parts of the developing skeleton, tail bud, major arteries, and heart (2‑5). In many of these areas, it is expressed along with FGF-8, but slightly later (2‑6). Unlike FGF-8 and FGF‑18, deletion of FGF‑17 produces viable mice. However, FGF‑17-/- mice show abnormalities in the dorsal frontal cortex, midbrain and cerebellum, manifested in some cases by ataxia, auditory defects, and abnormal social behavior (1, 4, 5, 8, 9). In the adult, FGF-17 is expressed in ovarian follicles and the prostate, and its expression is increased by both benign hypertrophy and cancer of the prostate (10‑12). FGF‑8, FGF‑17, and FGF‑18 are also abnormally expressed in many leukemic cell lines and can enhance growth of cancer cells (13).
- Itoh, N. and D.M. Ornitz (2008) Dev. Dyn. 237:18.
- Maruoka, Y. et al. (1998) Mech. Dev. 74:175.
- Xu, J. et al. (1999) Mech. Dev. 83:165.
- Cholfin, J.A. and J.L.R. Rubenstein (2007) Proc. Natl. Acad. Sci. USA 104:7652.
- Xu, J. et al. (2000) Development 127:1833.
- Olsen, S.K. et al. (2006) Genes Dev. 20:185.
- Zhang, X. et al. (2006) J. Biol. Chem. 281:15694.
- Yu, X. et al. (2011) Neuroimage 56:1251.
- Scearce-Levie, K. et al. (2008) Genes Brain Behav. 7:344.
- Machado, M.F. et al. (2009) J. Endocrinol. 202:347.
- Polnaszek, N. et al. (2004) Prostate 60:18.
- Heer, R. et al. (2004) J. Pathol. 204:578.
- Nezu, M. et al. (2005) Biochem. Biophys. Res. Commun. 335:843.
Citation for Recombinant Mouse FGF-17 Protein
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
1 Citation: Showing 1 - 1
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Heparan sulphate sulphation by Hs2st restricts astroglial precursor somal translocation in developing mouse forebrain by a non cell autonomous mechanism
Authors: JM Clegg, H Parkin, JO Mason, T Pratt
J. Neurosci., 2019-01-07;0(0):.
Species: Mouse
Sample Types: In Vivo
Applications: In Vivo
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