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MFN2 抗体 (AA 601-757) (PE)

This 兔 多克隆 antibody specifically detects MFN2 in FACS. It exhibits reactivity toward 人, 大鼠 和 小鼠.
产品编号 ABIN8010869
发货至: 中国
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Quick Overview for MFN2 抗体 (AA 601-757) (PE) (ABIN8010869)

抗原

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

适用

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人, 大鼠, 小鼠

宿主

  • 79
  • 31
  • 1

克隆类型

  • 65
  • 46
多克隆

标记

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This MFN2 antibody is conjugated to PE

应用范围

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Flow Cytometry (FACS)
  • 抗原表位

    • 24
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    AA 601-757

    原理

    Anti-Mitofusin 2/MFN2 Antibody PE Conjugated

    特异性

    No cross reactivity with other proteins.

    交叉反应 (详细)

    No cross-reactivity with other proteins

    预测反应

    Human Mitofusin 2 shares 96%,95% amino acid (aa) sequence identity with mouse,rat Mitofusin 2,respectively.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human Mitofusin 2 recombinant protein (Position: V601-R757). Human Mitofusin 2 shares 96% and 95% amino acid (aa) sequence identity with mouse and rat Mitofusin 2, respectively.

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    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

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

    MFN2 (Mitofusin 2 (MFN2))

    别名

    MFN2

    背景

    Background: Mitofusin-2 is a protein that in humans is encoded by the MFN2 gene. It is mapped to chromosome 1 and encodes a 757-amino acid protein that contains an ATP/GTP-binding site motif. This gene is expressed in many tissues and cell lines such as brain and KG-1 with the highest expression in heart and skeletal muscle. It has been found that MFN2 triggers mitochondrial energization, at least in part, by regulating OXPHOS expression through signals that are independent of its role as a mitochondrial fusion protein. And it contributes to the maintenance and operation of the mitochondrial network. Axonal CMT type 2A and autosomal dominant HMSN VI are caused by MFN2 and mutations in MFN2, which emphasizes its important role of mitochondrial function for both optic atrophies and peripheral neuropathies.

    Gene Full Name: mitofusin 2

    Sequence Similarities: Belongs to the TRAFAC class dynamin-like GTPase superfamily. Dynamin/Fzo/YdjA family. Mitofusin subfamily.

    基因ID

    9927

    UniProt

    O95140

    途径

    Skeletal Muscle Fiber Development
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