Thermo Fisher Scientific FGF13 Monoclonal Antibody (N235/22), FITC
FGF13 단백질을 특이적으로 인식하는 FITC 결합 단클론 항체입니다. Western blot, IHC, ICC/IF 등 다양한 응용에 사용 가능하며, 인간, 생쥐, 랫트에 반응합니다. 단백질 G로 정제된 액상 형태로 제공되며, 4°C 암소 보관이 권장됩니다.
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Applications and Tested Dilution
| Application | Tested Dilution | Notes |
|---|---|---|
| Western Blot (WB) | 1:1,000 | |
| Immunohistochemistry (IHC) | Assay-dependent | |
| Immunocytochemistry (ICC/IF) | Assay-dependent |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Mouse / IgG2b |
| Class | Monoclonal |
| Type | Antibody |
| Clone | N235/22 |
| Immunogen | Synthetic peptide amino acids 2–18 (AAAIASSLIRQKRQARE) of human FHF2A |
| Conjugate | FITC |
| Excitation / Emission Max | 498 / 517 nm |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein G |
| Storage Buffer | 9.1 mM sodium bicarbonate/PBS, pH 7.4, with 640.91 mM DMSO, 136.36 mM ethanolamine |
| Contains | No preservative |
| Storage Conditions | 4°C, store in dark |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2932106 |
Additional Formats Available
- Unconjugated (MA5-27705)
- APC (MA5-45651)
- PE (MA5-45654)
- PerCP (MA5-45653)
- Custom conjugation available upon request
Product Specific Information
- 100% identical to rat, 94% identical to mouse.
80% identity with FGF12A/FHF1A, FGF14A/FHF4A, and FGF11A/FHF3A.
- 1 µg/mL of MA5-45652 detects FGFA/FHFA (pan) in 20 µg of rat brain lysate by colorimetric immunoblot using Goat anti-mouse IgG:HRP as secondary antibody.
- Detects approximately 30 kDa.
- Does not cross-react with FGF13B/FHF2B.
- Cross-reacts with FGF12A/FHF1A and FGF14A/FHF4A.
- Formerly sold as clone S235-22.
Target Information
The protein encoded by this gene belongs to the fibroblast growth factor (FGF) family, which has broad mitogenic and cell survival activities. FGFs are involved in embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion.
This gene is located on chromosome X and is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a candidate gene for familial BFLS and other X-linked mental retardation syndromes.
Alternative splicing at the 5′ end results in multiple isoforms with different N-termini.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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