FGFR2 Antibody (YA439)
(Synonyms: CD332, BEK, KGFR, KSAM, FGFR2, Fibroblast growth factor receptor 2, FGFR-2, K-sam, Keratinocyte growth factor receptor)Based on 1 Customer Validation
FGFR2 Antibody (YA439) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to FGFR2.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB, IP
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Reactivity :
Human
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Formulation:
Supplied in 1*TBS (pH7.4), 0.05% BSA and 40% Glycerol. Preservative: 0.05% Sodium Azide.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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IP
IP: Immunoprecipitation
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| Dilution Ratio | 1:1000-1:2000 | 1:10-1:50 |
Product Details
FGFR2 Antibody (YA439) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to FGFR2.
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Host Rabbit
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Clonality Recombinant,Monoclonal
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Species ReactivityHuman
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Observed Molecular WeightObserved band size: 145 kDaNote: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
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Calculated Molecular Weight Predicted band size: 92 kDa
Synthetic peptide corresponding to Human FGFR2.AA range:30-70.
Endogenous
Protein A affinity purified.
Non-conjugated
Unmodified
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in 1*TBS (pH7.4), 0.05% BSA and 40% Glycerol. Preservative: 0.05% Sodium Azide.
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Concentration
Batch-dependent, Please check the COA for the concentration of each lot. Check Lot Concentration
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Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
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Shipping
Shipping with blue ice.
Verification Images
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Western blot analysis of extracts from HT-29 (lane 2(20μg) and HT-29 (lane 3(40μg)using FGFR2 (HY-P80397) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% defatted milk powder in TBST for 2 hour at room temperature. The primary antibody (HY-P80397, 1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/3000) was used in 5% defatted milk powder in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (HY-P8004/HY-P8001, 1/10,000) was used for 1 hour at room temperature.
Background
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Function
FGFR2 encodes FGFR2b and FGFR2c isoforms with distinct expression domains and ligand specificity[1]. Mechanistically, FGF/FGFR signaling regulates lineage commitment, differentiation, proliferation, and apoptosis in development and adult homeostasis[2]. In disease models, FGFR2 alterations activate signaling in breast, gastric, cholangiocarcinoma, lung squamous, and oral squamous cancers[1][3][4]. Compared with related isoforms, FGFR2b-to-FGFR2c switching occurs during prostate and bladder cancer progression, linking splice regulation to epithelial-mesenchymal transition[1]. For experimental applications, FGFR2 mutation or amplification supports use of FGFR inhibitors, while extracellular-domain FGFR2 mutations can drive constitutive dimerization and inhibitor-sensitive transformation[1][4].
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Subcellular Localization
Cell membrane; Single-pass type I membrane protein; Golgi apparatus; Cytoplasmic vesicle; Cell membrane; Single-pass type I membrane protein; Cell membrane; Single-pass type I membrane protein; Secreted; Secreted
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Isoforms & Post-Translational Modification
P21802 has 17 isomers: P21802-1: 92025 Da (predicted); P21802-2: 86130 Da (predicted); P21802-3: 92118 Da (predicted); P21802-4: 76705 Da (predicted); P21802-5: 91825 Da (predicted); P21802-6: 88181 Da (predicted); P21802-8: 85929 Da (predicted); P21802-14: 28299 Da (predicted); P21802-15: 79212 Da (predicted); P21802-16: 92153 Da (predicted); P21802-17: 86223 Da (predicted); P21802-18: 91918 Da (predicted); P21802-19: 40614 Da (predicted); P21802-20: 79197 Da (predicted); P21802-21: 79300 Da (predicted); P21802-22: 76423 Da (predicted); P21802-23: 79833 Da (predicted).
Autophosphorylated. Binding of FGF family members together with heparan sulfate proteoglycan or heparin promotes receptor dimerization and autophosphorylation on several tyrosine residues. Autophosphorylation occurs in trans between the two FGFR molecules present in the dimer. Phosphorylation at Tyr-769 is essential for interaction with PLCG1;N-glycosylated in the endoplasmic reticulum. The N-glycan chains undergo further maturation to an Endo H-resistant form in the Golgi apparatus;Ubiquitinated. FGFR2 is rapidly ubiquitinated after autophosphorylation, leading to internalization and degradation. Subject to degradation both in lysosomes and by the proteasome -
Subunit
Monomer. Homodimer after ligand binding. Interacts predominantly with FGF1 and FGF2, but can also interact with FGF3, FGF4, FGF6, FGF7, FGF8, FGF9, FGF10, FGF17, FGF18 and FGF22 (in vitro). Ligand specificity is determined by tissue-specific expression of isoforms, and differences in the third Ig-like domain are crucial for ligand specificity. Isoform 1 has high affinity for FGF1 and FGF2, but low affinity for FGF7. Isoform 3 has high affinity for FGF1 and FGF7, and has much higher affinity for FGF7 than isoform 1 (in vitro). Affinity for fibroblast growth factors (FGFs) is increased by heparan sulfate glycosaminoglycans that function as coreceptors. Likewise, KLB increases the affinity for FGF19 and FGF21. Interacts with PLCG1, GRB2 and PAK4. Interacts with FLRT2 (By similarity)
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SwissProt ID
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Synonyms
CD332, BEK, KGFR, KSAM, FGFR2, Fibroblast growth factor receptor 2, FGFR-2, K-sam, Keratinocyte growth factor receptor
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Research Field
Cardiovascular
Documentation
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Data Sheet (261 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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User Guide for Antibodies (1077 KB)
[1]. Katoh Y, et al. FGFR2-related pathogenesis and FGFR2-targeted therapeutics (Review). Int J Mol Med. 2009 Mar;23(3):307-11. [Content Brief]
[2]. Xie Y, et al. FGF/FGFR signaling in health and disease. Signal Transduct Target Ther. 2020 Sep 2;5(1):181. [Content Brief]
[3]. Egan JB, et al. Molecular Modeling and Functional Analysis of Exome Sequencing-Derived Variants of Unknown Significance Identify a Novel, Constitutively Active FGFR2 Mutant in Cholangiocarcinoma. JCO Precis Oncol. 2017;2017. [Content Brief]
[4]. Liao RG, et al. Inhibitor-sensitive FGFR2 and FGFR3 mutations in lung squamous cell carcinoma. Cancer Res. 2013 Aug 15;73(16):5195-205. [Content Brief]