
Thermo Fisher Scientific MFN2 Monoclonal Antibody (N153/5), PE
MFN2 단백질을 인식하는 PE 결합 단클론 항체로, Western blot, IHC, ICC/IF에 사용 가능. 인간, 마우스, 랫트 반응성. 단백질 G로 정제된 액상 포맷, 보존제 없음. 미토콘드리아 융합 연구 및 MFN2 관련 질환 연구에 적합.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:1,000 |
| Immunohistochemistry (IHC) | Assay-dependent |
| Immunocytochemistry (ICC/IF) | 1:100 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Mouse / IgG2a |
| Class | Monoclonal |
| Type | Antibody |
| Clone | N153/5 |
| Immunogen | Fusion protein amino acids 370–600 (cytoplasmic N-terminus) of mouse Mitofusin-2 |
| 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_2932126 |
Available Formats
- Unconjugated (MA5-27647)
- APC (MA5-45669)
- FITC (MA5-45670)
- PerCP (MA5-45671)
- Request custom conjugation
Product Specific Information
- Rat: 97% identity (226/231 amino acids identical)
- Human: 92% identity (214/231 amino acids identical)
- ~55% identity with Mitofusin-1
- Detects approximately 90 kDa
- No cross-reactivity against Mitofusin-1
- 1 µg/mL of MA5-45672 was sufficient for detection of Mitofusin-2 in 20 µg of mouse cardiac mitochondrial lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody
- This antibody was formerly sold as clone S153-5
Target Information
This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. It regulates vascular smooth muscle cell proliferation and may play a role in obesity-related pathophysiology. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2 and hereditary motor and sensory neuropathy VI, both disorders of the peripheral nervous system. Defects have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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