Recombinant Human FGFR1 alpha (IIIc) His-tag Protein, CF

R&D Systems, part of Bio-Techne | Catalog # 11118-FR

R&D Systems, part of Bio-Techne
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11118-FR-050
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Key Product Details

Source

HEK293

Accession #

P11362.3

Conjugate

Unconjugated

Applications

Bioactivity

View all FGFR1 alpha Proteins and Enzymes »

Product Specifications

Source

Human embryonic kidney cell, HEK293-derived human FGFR1 alpha protein
Arg22-Glu376, with a C-terminal 6-His tag

Purity

>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.

Endotoxin Level

<0.10 EU per 1 μg of the protein by the LAL method.

N-terminal Sequence Analysis

Arg22

Predicted Molecular Mass

40 kDa

SDS-PAGE

70-85 kDa, under reducing conditions.

Activity

Measured by its binding ability in a functional ELISA.
In a Human FGF acidic/FGF1 antibody (Catalog # AF232) coated plate, in the presence of 50.0 ng/mL of Recombinant Human FGF acidic/FGF1 (Catalog # 232-FA), Human FGFR1 alpha (IIIc) His-tag Protein binds with an ED50 of 1.00-5.00 µg/mL.

Scientific Data Images for Recombinant Human FGFR1 alpha (IIIc) His-tag Protein, CF

Recombinant Human FGFR1 alpha (IIIc) His-tag Protein Binding Activity.

In a Human FGF acidic/FGF1 antibody (AF232) coated plate, in the presence of 50.0 ng/mL of Recombinant Human FGF acidic/FGF1 (232-FA), Human FGFR1 alpha (IIIc) His-tag Protein (Catalog # 11118-FR) binds with an ED50 of 1.00-5.00 µg/mL.

Recombinant Human FGFR1 alpha (IIIc) His-tag Protein SDS-PAGE.

2 μg/lane of Recombinant Human FGFR1 alpha (IIIc) His-tag Protein (Catalog # 11118-FR) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands at 70-85 kDa.

Formulation, Preparation and Storage

11118-FR
Formulation Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose.
Reconstitution Reconstitute at 500 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.
  • 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.

Background: FGFR1 alpha

Fibroblast growth factor receptor 1 (FGFR1) belongs to a family of type I transmembrane tyrosine kinases which mediate the biological functions of FGFs that are involved in a multitude of physiological and pathological cellular processes (1). The FGFR family is comprised of 4 structurally conserved members (FGFR1-4) all possessing an extracellular domain (ECD) with three immunoglobulin (Ig)-like domains, an acid-box region containing a run of acidic residues between the IgI and IgII domains, a transmembrane domain and cytoplasmic split tyrosine-kinase domain (1, 2). The ECD of mature, full-length FGFR1 shares 98% amino acid sequence identity with mouse FGFR1. Alternative splicing generates multiple forms of FGFR1-3, each with unique signaling characteristics (1-3). For FGFR1, alternative splicing of the ECD generates FGFR1A, FGFR1B, and FGFR1G isoforms of the receptor with the A isoform containing three Ig domains, while the B and G isoforms lack the N‑terminal IgI domain (3). Additional splicing of the IgIII domain, results in IIIa, IIIb, or IIIc isoforms (3). Only the alpha isoform has been identified for FGFR3 and FGFR4 and FGFR4 also lacks the IIIb and IIIc splicing events (4). The FGFR splice variants also exhibit distinct and varying binding affinities for different FGF ligands (2). FGFRs mediate the FGF signaling cascade which regulate developmental processes including cellular proliferation, differentiation, and migration, morphogenesis, and patterning (5). FGFRs transduce the signals through three dominant pathways including RAS/MAPK, PI3k/AKT, and PLC gamma (6). FGFR1 the most abundant FGFR and is widely expressed in many adult human tissues, but the splice variants display distinct tissue-specific differences with IIIc splice variants expressed in mesenchymal tissue (4, 7, 8). Mutations in FGFR1 or misregulation of FGFR1 mediated signaling is found in multiple diseases, with FGFR1A(IIIc) specifically upregulated, from breast and pancreatic cancer to Pfeiffer syndrome and osteoarthritis (4, 9-11). A soluble version of the FGFR1A(IIIc) splice variant has shown anti-angiogenic and anti-proliferative properties in multiple cancer cell line models (11).

References

  1. Ornitz, D.M. and Itoh, N. (2015) Wiley Interdiscip. Rev. Dev. Biol. 4:215.
  2. Zhang, X. et al. (2006) J Biol. Chem. 281:15694.
  3. Ferguson, H.R. et al. (2021) Signaling Cells 10:1201.
  4. Holzmann, K. et al. (2012) J Nucleic. Acids 2012:950508.
  5. Xie, Y. et al. (2020) Sig. Transduct. Target Ther. 5:181.
  6. Mossahebi-Mohammadi, M. et al. (2020) Front Cell Dev. Biol. 18:79.
  7. Hughes, S.E. (1997) J. Histochem. Cytochem. 45:1005.
  8. Delezoide, A.L. et al. (1998) Mech. Dev. 77:19.
  9. Yamashita-Sugahara, Y. et al. (2016) Sci. Rep. 6:35908.
  10. Teven, C.M. et al. (2014) Genes Dis. 1:199.
  11. Babina, I. and Turner, N. (2017) Nat. Rev Cancer 17:318.

Long Name

Fibroblast Growth Factor Receptor 1 alpha

Alternate Names

FGF R1a

UniProt

P11362.3

Additional FGFR1 alpha Products

Product Documents for Recombinant Human FGFR1 alpha (IIIc) His-tag Protein, CF

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