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

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MFN2 단백질 검출용 마우스 단클론 항체로, Western blot, IHC, ICC/IF에 적합. 인간, 마우스, 랫트 반응성. 단백질 G 정제, PBS/glycerol buffer 보존. 미토콘드리아 융합 연구 및 신경 질환 관련 연구에 활용 가능.

카탈로그번호
MA527647
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 08:16
Thermo Fisher Scientific MA527647 MFN2 Monoclonal Antibody (N153/5) 100 ug pk판매 단위 pk ·
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775,200원VAT 포함 852,720원

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

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:1,000 View 2 publications
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1:100 -
Immunocytochemistry (ICC/IF) 1:100 -

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Published Species Human
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. Rat: 97% identity (226/231 aa identical). Human: 92% identity (214/231 aa identical), ~55% identity with Mitofusin-1.
Conjugate Unconjugated
Available Conjugates APC, FITC, PE, PerCP, Request custom conjugation
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_2735272

Product Specific Information

  • 1 µg/mL of MA5-27647 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.
  • Detects approximately 90 kDa.
  • No cross-reactivity against Mitofusin-1.
  • This antibody was formerly sold as 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 is involved in the regulation of vascular smooth muscle cell proliferation and may play a role in obesity-related pathophysiology.
Mutations 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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