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MFN2 抗体

MFN2 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6290636
发货至: 中国
  • 抗原 See all MFN2 抗体
    MFN2 (Mitofusin 2 (MFN2))
    适用
    • 75
    • 52
    • 36
    • 20
    • 4
    • 4
    • 4
    • 4
    • 3
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    • 2
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    • 2
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    人, 小鼠, 大鼠
    宿主
    • 62
    • 32
    • 2
    克隆类型
    • 63
    • 33
    多克隆
    标记
    • 35
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    • 1
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    This MFN2 antibody is un-conjugated
    应用范围
    • 85
    • 46
    • 34
    • 23
    • 22
    • 16
    • 16
    • 13
    • 13
    • 8
    • 3
    • 1
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    Western Blotting (WB), Immunohistochemistry (IHC)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of mouse MFN2
    亚型
    IgG
    Top Product
    Discover our top product MFN2 Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    IHC 1:50 - 1:200
    限制
    仅限研究用
  • 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 -20C. Avoid freeze / thaw cycles.
  • 抗原
    MFN2 (Mitofusin 2 (MFN2))
    别名
    MFN2 (MFN2 产品)
    别名
    CG3869 antibody, Dmel\\CG3869 antibody, MARF antibody, Marf-1 antibody, Mfn antibody, anon-WO0125274.3 antibody, dMFN antibody, dMfn antibody, dmfn antibody, marf antibody, mfn antibody, mfn2 antibody, MFN2 antibody, hsg antibody, cmt2a antibody, cprp1 antibody, cmt2a2 antibody, CMT2A antibody, CMT2A2 antibody, CPRP1 antibody, HSG antibody, D630023P19Rik antibody, Fzo antibody, mg:cb01g09 antibody, si:dkeyp-104h9.2 antibody, wu:fb79a11 antibody, mitofusin 2 antibody, Mitochondrial assembly regulatory factor antibody, mitofusin-2 antibody, mitofusin 2 L homeolog antibody, MFN2 antibody, Marf antibody, mfn2 antibody, LOC100186475 antibody, Mfn2 antibody, mfn2.L antibody
    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.
    途径
    Skeletal Muscle Fiber Development
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