Thermo Fisher Scientific FGF13 Monoclonal Antibody (N235/22), PerCP
FGF13 단백질을 인식하는 PerCP 결합 단일클론 항체로, Western blot, IHC, ICC/IF 등에 사용 가능. 인간, 마우스, 랫트 반응성. 단백질 G 정제, 보존제 없음. 4°C 보관, 연구용 전용.
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Applications
| Application | Tested Dilution | Publications |
|---|---|---|
| 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 | PerCP |
| Excitation / Emission Max | 482 / 675 nm |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein G |
| Storage Buffer | 95.64 mM phosphate / 2.48 mM MES, pH 7.4, with 0.5 M EDTA |
| Contains | No preservative |
| Storage Conditions | 4°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2932107 |
Additional Formats
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 MA5-45653 was sufficient for detection of FGFA/FHFA (pan) in 20 µg of rat brain lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody.
- Detects approximately 30 kDa.
- Does not cross-react with FGF13B/FHF2B.
- Cross-reacts with FGF12A/FHF1A and FGF14A/FHF4A.
- This antibody was formerly sold as clone S235-22.
Target Information
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in various biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion.
This gene is located on the X chromosome region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate for familial cases of BFLS and other X-linked intellectual disability syndromes.
Alternative splicing at the 5′ end results in several transcript variants encoding different 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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