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Thermo Fisher Scientific Mitofusin 2 Polyclonal Antibody
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Thermo Fisher Scientific Mitofusin 2 Polyclonal Antibody

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Mitofusin 2 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체. Western blot 및 IHC(P)에서 검증됨. 인간, 마우스, 랫트 반응성. 합성 펩타이드 면역원 사용. 냉장 및 냉동 보관 가능, 연구용 전용.

카탈로그번호
OSM00097W-100UL
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 06:19
Thermo Fisher Scientific OSM00097W-100UL Mitofusin 2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific Mitofusin 2 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:300–1:2,000 -
Immunohistochemistry (Paraffin) (IHC (P)) 1:1,000 -
Miscellaneous PubMed (Misc) - View 3 publications

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from internal region of mouse Mitofusin 2 (Mitochondrial assembly regulatory factor) conjugated to an immunogenic carrier protein
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Storage Buffer Whole serum
Contains No preservative
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. Glycerol (1:1) may be added for added stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
Specificity of this antibody: Mitofusin 2

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 the pathophysiology of obesity.
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 in this gene 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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