Thermo Fisher Scientific FGF13 Monoclonal Antibody (N235/22), PE
FGF13 단백질을 인식하는 PE 결합 단클론 항체로, 사람·생쥐·쥐 시료에 반응합니다. WB, IHC, ICC 등 다양한 응용에 적합하며, 단백질 G로 정제된 액상 형태입니다. 4°C에서 보관하며, 형광 특성은 565/576 nm입니다.
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Applications and Tested Dilution
| 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 | PE (R-Phycoerythrin) |
| Excitation / Emission Max | 565 / 576 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_2932108 |
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 MA5-45654 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 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 is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion.
This gene is located on chromosome X and has been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), suggesting potential involvement in familial or syndromal forms of X-linked mental retardation.
Alternative splicing at the 5′ end results in multiple transcript variants encoding 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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