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

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MFN2 단일클론 항체(N153/5), PerCP 형으로 인간, 마우스, 랫트 시료에 반응. Western blot, IHC, ICC/IF 등 다양한 응용에 적합. 단백질 G 정제, 보존제 없음, 4°C 보관. 미토콘드리아 융합 및 신경계 질환 연구용.

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pk
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마지막 업데이트 2025. 08. 04. 오후 06:46
Thermo Fisher Scientific MA545671 MFN2 Monoclonal Antibody (N153/5), PerCP 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), PerCP

Applications

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 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_2932125

Additional 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
  • 1 µg/mL of MA5-45671 detects Mitofusin-2 in 20 µg of mouse cardiac mitochondrial lysate by colorimetric immunoblot using Goat anti-mouse IgG:HRP as secondary antibody
  • Detects approximately 90 kDa
  • No cross-reactivity against Mitofusin-1
  • 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 pathophysiology.
Mutations cause Charcot-Marie-Tooth disease type 2A2 and hereditary motor and sensory neuropathy VI, both peripheral nervous system disorders. Defects are also 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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