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Thermo Fisher Scientific MFN2 Monoclonal Antibody (N153/5), PE
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Thermo Fisher Scientific MFN2 Monoclonal Antibody (N153/5), PE

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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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pk
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마지막 업데이트 2025. 08. 05. 오후 12:55
Thermo Fisher Scientific MA545672 MFN2 Monoclonal Antibody (N153/5), PE 100 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

Thermo Fisher Scientific · Thermo Fisher Scientific MFN2 Monoclonal Antibody (N153/5), PE

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


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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