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Description
Images & Validation
−| Tested Applications | IF, IHC, WB |
|---|---|
| Dilution range | WB: 1-500-1-1000, IHC-P: 1-100-1-200 |
| Reactivity | Bovine, Canine, Human, Mouse, Porcine, Rat |
Key Properties
−| Antibody Type | Primary Antibody |
|---|---|
| Host | Rabbit |
| Clonality | Polyclonal |
| Immunogen | KLH-conjugated synthetic peptide encompassing a sequence within the center region of human FGFR3. The exact sequence is proprietary. |
| Purification | The antibody was purified by immunogen affinity chromatography. |
| Conjugation | Unconjugated |
Storage & Handling
−| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
|---|---|
| Form/Appearance | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
| Disclaimer | For research use only |
Alternative Names
−Similar Products
−Mouse Fibroblast Growth Factor Receptor 3 (FGFR3) ELISA Kit [orb778191]
Mouse
0.16-10 ng/mL
0.058 ng/mL
48 T, 96 THuman Fibroblast Growth Factor Receptor 3 (FGFR3) ELISA Kit [orb777024]
Human
0.16-10 ng/mL
0.06 ng/mL
48 T, 96 T

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Western blot analysis of FGFR3 expression in A549 (A), HEK293T (B), HCT116 (C), PC12 (D), CT26 (E) whole cell lysates. (Predicted band size: 87 kD; Observed band size: 97; 125 kD)

Immunohistochemical analysis of FGFR3 staining in human breast cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunofluorescent analysis of FGFR3 staining in MCF7 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).
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Protocol Information
FGFR3 Antibody (orb213929)
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