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MFN2 抗体 (AA 500-600)

This anti-MFN2 antibody is a 兔 多克隆 antibody detecting MFN2 in WB, IHC 和 IF. Suitable for 人.
产品编号 ABIN6143800
发货至: 中国

Quick Overview for MFN2 抗体 (AA 500-600) (ABIN6143800)

抗原

See all MFN2 抗体
MFN2 (Mitofusin 2 (MFN2))

适用

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宿主

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克隆类型

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多克隆

标记

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This MFN2 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • 抗原表位

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    AA 500-600

    序列

    GLKPLLPVSV RSQIDMLVPR QCFSLNYDLN CDKLCADFQE DIEFHFSLGW TMLVNRFLGP KNSRRALMGY NDQVQRPIPL TPANPSMPPL PQGSLTQEEF M

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    免疫原

    A synthetic peptide corresponding to a sequence within amino acids 500-600 of human Mitofusin 2 (NP_001121132.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    MFN2 (Mitofusin 2 (MFN2))

    别名

    MFN2

    背景

    This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it 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, which are 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.,CMT2A,CMT2A2,CMT2A2A,CMT2A2B,CPRP1,HMSN6A,HSG,MARF,MFN2,Mitofusin 2,Cancer,Signal Transduction,Cell Biology & Developmental Biology,Apoptosis,Autophagy,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Mitophagy fission and fusion,Neuroscience,Neurodegenerative Diseases,Mitochondrial Control of Autophagy,MFN2

    分子量

    50 kDa/86 kDa

    基因ID

    9927

    UniProt

    O95140

    途径

    Skeletal Muscle Fiber Development
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