Recombinant Human KGF/FGF-7 Protein, CF New
Recombinant Human KGF/FGF-7 Protein, CF Summary
Product Specifications
Ser55-Thr194
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.
11537-KG
Formulation | Lyophilized from a 0.2 μm filtered solution in MOPS, Na2SO4 and EDTA with Trehalose. |
Reconstitution | Reconstitute 10 μg size at 100 μg/mL and the other sizes at 200 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.
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Scientific Data
Measured in a cell proliferation assay using Ba/F3 mouse pro B cells transfected with human FGF RIIb. The ED50 for this effect is 4.00-40.0 ng/mL.
2 μg/lane of Recombinant Human KGF/FGF‑7 Protein (Catalog # 11537-KG) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands at 15-18 kDa, under reducing conditions.
Reconstitution Calculator
Background: KGF/FGF-7
Fibroblast growth factor 7 (FGF7), also known as keratinocyte growth factor (KGF), is a member of the FGF family of secreted glycoproteins which are involved in key roles from development, morphogenesis, and angiogenesis to wound healing and tumorigenesis (1-4). FGF7, along with FGF3, FGF10, and FGF22, form a subfamily of the larger FGF family whose expression is restricted to cells of mesenchymal origin and function as paracrine growth factors for nearby epithelial cells (1). The FGF family is characterized by a core heparin-binding FGF domain of approximately 120 amino acids (aa) that exhibits a conserved beta -trefoil structure (2). Mature human FGF7 shares 96% and 92% aa sequence identity with mouse and rat FGF7, respectively. FGF7 signals only through the IIIb splice form of the receptor FGFR2, whose expression is restricted primarily to epithelial cells (5). FGF7 is noticeably upregulated in response to damage to skin or internal structures and is proposed to help speed-up wound healing (6). Deletion of FGF7 affects kidney development, producing abnormally small ureteric buds and fewer nephrons (7). FGF7 has been proposed as a potential cancer therapeutic by targeting the intermolecular interaction site between FGF7 and FGFR2b (3). Additionally, the use of FGF7 is being explored as novel treatment options for cartilage diseases, such as Osteoarthritis and Rheumatoid arthritis (8). An N-terminally truncated version of FGF7 with improved thermal stability, named Palifermin (brand name Kepivance), is approved for treatment for reducing and/or healing damages caused by cancer chemotherapy and radiotherapy, such as severe oral mucositis (OM) (9,10).
- Mohammadi, M. et al. (2005) Cytokine Growth Factor Rev. 16:107.
- Itoh, N. and D.M. Ornitz (2008) Dev. Dyn. 237:18.
- Vadija, R. et al. (2016) J. Chem. Biol. 9:69.
- Itoh, N. and D.M. Ornitz (2004). Trends Genet. 20:563.
- Steiling, H. and S. Werner (2003) Curr. Opin. Biotechnol. 14:533.
- Geer, D.J. et al. (2005) Am. J. Pathol. 167:1575.
- Qiao, J. et al. (1999) Development 126:547.
- Zhang, X. et al. (2023) Life Sci. 326:121804.
- Hsu, E. et al. (2006) PEDS 19:147.
- Sadeghi, S. et al. (2021) Int. J. Biol. Macromol. 191:1175.
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