FGF10 antibodies are immunoglobulin-based reagents designed to detect and quantify FGF10 in experimental settings. These antibodies bind specifically to FGF10, enabling its visualization in assays such as Western blot (WB), immunohistochemistry (IHC), and enzyme-linked immunosorbent assay (ELISA). FGF10 is encoded by the FGF10 gene (UniProt ID: O15520) and shares 92–95% sequence homology across human, mouse, and rat species .
FGF10 antibodies are widely used in:
Developmental Biology: Studying limb bud formation, lung branching morphogenesis, and salivary gland development .
Cancer Research: Investigating FGF10/FGFR2 signaling in cholangiocarcinoma (CCA) metastasis and therapeutic targeting .
Inflammation Studies: Analyzing cross-talk between FGF10 and immune responses in lung injury and fibrosis .
In CCA: FGF10 promotes metastasis via Akt/mTOR and VEGF/Slug pathways. FGFR inhibitors (e.g., infigratinib) suppress FGF10-driven cell migration .
Lung Development: Fgf10 heterozygosity alters immune gene expression in alveolar type 2 (AT2) cells, exacerbating hyperoxia-induced injury .
Wound Healing: FGF10 mitigates inflammation by blocking HMGB1 translocation in bronchial epithelial cells .
Western Blot: Detects FGF10 at ~20–40 kDa in lung carcinoma (A549) and HEK-293 cells .
IHC: Localizes FGF10 in human prostate tissue and mouse embryonic spinal cord .
ELISA: Paired antibodies (e.g., AF345 + MAB3451) achieve high sensitivity in FGF10 quantification .
Cross-Reactivity: Some antibodies cross-react with FGF7 due to structural homology .
Storage: Sodium azide (0.02–0.1%) is recommended for preservation but requires careful handling .
Species Specificity: Mouse-specific antibodies (e.g., AF6224) show <100% cross-reactivity with rat FGF10 .
When investigating FGF10's role in epithelial-mesenchymal crosstalk, prioritize antibodies validated for species-specific reactivity and application compatibility. For mouse embryonic studies, the AF6224 antibody detects FGF10 in frozen sections of E13 embryos with localization to spinal cord tissues . In human cancer models, MAB3451 demonstrates specificity for recombinant human FGF10 (Cys37-Ser208) and pairs with AF345 for ELISA development . Cross-reactiveness assessments should include:
Methodological Tip: Pre-test antibodies in knockout controls (e.g., Fgf10−/− mice) to confirm absence of non-specific binding .
Non-specific bands in WB often arise from post-translational modifications or antibody cross-reactivity. The AF6224 antibody detects a single 20 kDa band in A549 lung carcinoma lysates under reducing conditions , while DF6333 identifies a 23 kDa isoform in human tissues due to glycosylation variance . To resolve discrepancies:
Use deglycosylation enzymes (e.g., PNGase F) to distinguish glycosylated vs. core protein forms .
Compare migration patterns across buffer systems (e.g., Immunoblot Buffer Group 8 reduces aberrant migrations) .
In pancreatic ductal adenocarcinoma (PDAC), FGF10 serum levels correlate with tumor progression. A multiplex approach combines:
ELISA: MAB3451/AF345 pair detects FGF10 at sensitivities of 15.6–1,000 pg/mL .
Spatial IHC: Localize FGF10-producing fibroblasts using AF6224 (5 µg/mL, overnight incubation at 4°C) with tyramide signal amplification .
Single-cell RNA-seq: Identify FGF10-expressing stromal cells (e.g., macrophages) in PDAC biopsies .
Conflicting reports on FGF10’s role in ER+ vs. basal-like breast cancers necessitate careful experimental design:
Advanced Tip: Use proximity ligation assays (PLA) to visualize FGF10-FGFR2b interactions in situ .
FGF10 shares 53% homology with FGF7, risking antibody cross-reactivity. Mitigation strategies include:
Peptide Blocking: Pre-incubate DF6333 with FGF7/FGF22 peptides (10-fold molar excess) .
Kinase Activity Assays: Verify functional specificity by measuring ERK1/2 phosphorylation exclusively in FGFR2b-transfected cells .
For embryonic lung branching morphogenesis:
Fixation: Immersion-fix E13 mouse embryos in 4% PFA for 24 hr .
Staining: AF6224 (5 µg/mL) + Anti-Sheep HRP-DAB Kit, with hematoxylin counterstain .
Validation: Compare signal distribution in Fgf10+/+ vs. Fgf10−/− littermates .
To dissect FGF10-FGFR2b signaling:
Co-Immunoprecipitation (Co-IP): Use MAB3451 to pull down FGF10-FGFR2b complexes from MDA-MB-231 lysates .
Phosphoproteomics: Map ERK/MAPK activation using phospho-specific antibodies post-FGF10 stimulation (10 ng/mL, 15 min) .
Reported FGF10 molecular weights vary:
| Source | Observed MW (kDa) | Conditions |
|---|---|---|
| A549 cells (AF6224) | 20 | Reducing, Immunoblot Buffer 8 |
| Human serum (DF6333) | 23 | Non-reducing, RIPA buffer |
Solution: Include recombinant FGF10 (20 kDa, R&D Systems #345-FG) as a migration control .
In gastric cancer microenvironments:
CyTOF: Stain FFPE sections with AF6224 (Metal-conjugated, 1:100) and panel of 35 metal-tagged antibodies .
Spectral Flow Cytometry: Combine DF6333 (APC) with PD-L1 (FITC) to correlate FGF10+ fibroblasts with immune evasion .
When using xenograft models: