1. Protein Tyrosine Kinase/RTK Stem Cell/Wnt MAPK/ERK Pathway
  2. FGFR ERK
  3. GP369

GP369 is a humanized FGFR2-IIIb-specific antibody. GP369 significantly inhibits the proliferation of tumor cells. GP369 can significantly inhibit phosphorylation of FGFR2 and downstream signaling pathways. GP369 can be used for research on cancer such as gastric cancer and breast cancer.

For research use only. We do not sell to patients.

GP369 Chemical Structure

GP369 Chemical Structure

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Description

GP369 is a humanized FGFR2-IIIb-specific antibody. GP369 significantly inhibits the proliferation of tumor cells. GP369 can significantly inhibit phosphorylation of FGFR2 and downstream signaling pathways. GP369 can be used for research on cancer such as gastric cancer and breast cancer[1].

IC50 & Target[1]

FGFR2

 

In Vitro

GP369 (0.001-1000 nM, 2-5 days) can significantly inhibit the proliferation of various cells, including FDCP-1, SUM52PE and MCF7 cells[1].
GP369 (0.001-100 nM, 2 days) inhibits FGFR2 IIIb driven proliferation and has no effect on FGFR2 IIIc in FDCP-1 (IC50 = 1.4 nM) cells[1].
GP369 (30 μg/mL, 3 days) inhibits proliferation induced by FGF7 (25 ng/mL) in MCF7 cells[1].
GP369 (10 μg/mL, 1-48 h) suppresses FGFR2 and ERK1/2 phosphorylation and downstream signaling in Ba/F3 and SNU-16 cells[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Proliferation Assay[1]

Cell Line: FDCP-1 cells
Concentration: 0.001-100 nM
Incubation Time: 2 days
Result: Significantly inhibited FGFR2 IIIb driven proliferation, including FGFR2 IIIb WT, FGFR2 IIIb N550K and FGFR2 IIIb S252W.

Western Blot Analysis[1]

Cell Line: SNU-16 cells
Concentration: 10 μg/mL
Incubation Time: 2, 6, 24 and 48 h
Result: Reduced the level of FGFR2 protein.

Western Blot Analysis[1]

Cell Line: Ba/F3 cells and SNU-16 cells
Concentration: 5 μg/mL
Incubation Time: Incubated for1 h and then combinated with FGF7 for 15 min
Result: Significantly inhibited FGF7 induced phosphorylation and downstream protein levels, including p-FGFR and p-ERK1/2.
In Vivo

GP369 (2-20 mg/kg; i.p.; twice weekly; for 43 days) significantly inhibits tumor growth and reduces FGFR2 phosphorylation and protein levels in C.B-17 severe combined immunodeficient (SCID) mice bearing SNU-16 xenografts[1].
GP369 (20 mg/kg, i.p.; twice weekly; for 27 days) realizes tumor arrest and significantly reduces FGFR2 phosphorylation and protein levels in NCr nude mice bearing MFM-223 xenografts[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female C.B-17 SCID mice bearing 5×106 SNU-16 cells (10 weeks)[1]
Dosage: 2, 5, 10 and 20 mg/kg
Administration: Intraperitoneal injection (i.p.); twice weekly for 43 days
Result: Significantly inhibited changes in tumor volume.
Significantly reduced the level of FGFR2 and p-FGFR.
Animal Model: 1×107 MFM-223 cells injected female NCr nude mice (5 weeks)[1]
Dosage: 20 mg/kg
Administration: Intraperitoneal injection (i.p.); twice weekly for 27 days
Result: Significantly inhibited changes in tumor volume.
Significantly reduced the level of FGFR2 and p-FGFR.
Gene ID

2263  [NCBI]

Accession
Target

FGFR2/CD332

Application

ELISA, FACS, Functional assay

Conjugated

Unconjugated

Reconsititution

The product can be reconstituted/diluted with sterile PBS or saline.

SMILES

N/A

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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GP369
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HY-P991583
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