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Thermo Fisher Scientific MFN2 Recombinant Rabbit Monoclonal Antibody (7H42L13)
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Thermo Fisher Scientific MFN2 Recombinant Rabbit Monoclonal Antibody (7H42L13)

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MFN2 단백질을 인식하는 재조합 토끼 단클론 항체로, Western blot에 적합합니다. Expi293 시스템에서 발현되며 높은 특이성과 일관된 로트 간 품질을 제공합니다. 인간, 생쥐 반응성이 검증되었으며 단기 4°C, 장기 -20°C 보관 권장.

카탈로그번호
702768
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 05:48
Thermo Fisher Scientific 702768 MFN2 Recombinant Rabbit Monoclonal Antibody (7H42L13) 100 ug pk판매 단위 pk ·
재고 확인 필요
631,500원VAT 포함 694,650원

Thermo Fisher Scientific · Thermo Fisher Scientific MFN2 Recombinant Rabbit Monoclonal Antibody (7H42L13)

Applications

Western Blot (WB)


Product Specifications

항목 내용
Species Reactivity Human, Mouse
Published Species Rat
Host / Isotype Rabbit / IgG
Expression System Expi293
Class Recombinant Monoclonal
Type Antibody
Clone 7H42L13
Immunogen Peptides corresponding to human Mitofusin 2 (aa391–aa410, aa742–aa757)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7.4
Contains 0.09% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2734817

Product Specific Information

  • This antibody is predicted to react with Monkey, Dog, Cat, and Bovine.
  • Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems by cloning specific antibody DNA sequences from immunoreactive rabbits.
  • Advantages include:
    • High specificity and sensitivity
    • Lot-to-lot consistency
    • Animal origin-free formulation
    • Broad immunoreactivity due to the rabbit immune repertoire

Target Information

This gene encodes a mitochondrial membrane protein involved in mitochondrial fusion and maintenance of the mitochondrial network. It regulates vascular smooth muscle cell proliferation and may play a role in obesity pathophysiology. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2 and hereditary motor and sensory neuropathy VI, both affecting the peripheral nervous system. Defects have also been linked to 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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