Thermo Fisher Scientific FGF13 Monoclonal Antibody (N235/22)
FGF13 단백질을 특이적으로 인식하는 Mouse monoclonal antibody입니다. Western blot, IHC, ICC에 사용 가능하며 Human, Mouse, Rat에 반응합니다. Protein G 정제, 1 mg/mL 농도의 액상 형태로 제공되며 -20°C에서 보관합니다.
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Applications and Tested Dilutions
| Application | Tested Dilution | Publications |
|---|---|---|
| Western Blot (WB) | 1:1,000 | View 1 publication |
| Immunohistochemistry (PFA fixed) (IHC (PFA)) | 1:100 | - |
| Immunocytochemistry (ICC/IF) | Assay-Dependent | - |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Published Species | Not Applicable |
| Host / Isotype | Mouse / IgG2b |
| Class | Monoclonal |
| Type | Antibody |
| Clone | N235/22 |
| Immunogen | Synthetic peptide amino acids 2–18 (AAAIASSLIRQKRQARE) of human FHF2A. 100% identical to rat, 94% identical to mouse. >80% identity with FGF12A/FHF1A, FGF14A/FHF4A, and FGF11A/FHF3A. |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein G |
| Storage Buffer | PBS, pH 7.4, with 50% glycerol |
| Contains | 0.1% sodium azide |
| Storage Conditions | -20°C |
| Shipping Conditions | Wet ice |
| RRID | AB_2735180 |
Additional Formats Available:
Product Specific Information
- 1 µg/mL of MA5-27705 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 chromosome X, associated with Borjeson-Forssman-Lehmann syndrome (BFLS), and may be a candidate gene for familial or syndromal forms of X-linked mental retardation.
Alternative splicing at the 5′ end results in several transcript variants encoding different isoforms with distinct N-termini.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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