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AFG3L2 抗体

AFG3L2 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN4950041
发货至: 中国
  • 抗原 See all AFG3L2 抗体
    AFG3L2 (AFG3-Like Protein 2 (AFG3L2))
    适用
    • 43
    • 7
    • 7
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
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    人, 小鼠, 大鼠
    宿主
    • 41
    • 3
    克隆类型
    • 43
    • 1
    多克隆
    标记
    • 21
    • 5
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    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
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    This AFG3L2 antibody is un-conjugated
    应用范围
    • 33
    • 23
    • 22
    • 8
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Antigen affinity
    免疫原
    Amino acids R168-D250 of the human protein were used as the immunogen for the AFG3L2 antibody.
    亚型
    IgG
    Top Product
    Discover our top product AFG3L2 Primary Antibody
  • 应用备注
    Optimal dilution of the AFG3L2 antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL
    限制
    仅限研究用
  • 缓冲液
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    储存条件
    -20 °C
    储存方法
    After reconstitution, the AFG3L2 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 抗原
    AFG3L2 (AFG3-Like Protein 2 (AFG3L2))
    别名
    AFG3L2 (AFG3L2 产品)
    别名
    MGC147390 antibody, si:ch211-12e1.4 antibody, SCA28 antibody, SPAX5 antibody, 2310036I02Rik antibody, AW260507 antibody, Emv66 antibody, par antibody, AFG3 like matrix AAA peptidase subunit 2 antibody, AFG3-like protein 2 antibody, AFG3 ATPase family gene 3-like 2 (S. cerevisiae) antibody, AFG3-like AAA ATPase 2 antibody, AFG3-like AAA ATPase 2 L homeolog antibody, AFG3L2 antibody, LOC578526 antibody, afg3l2 antibody, afg3l2.L antibody, Afg3l2 antibody
    背景
    AFG3L2 is the catalytic subunit of the m-AAA protease, an ATP-dependent proteolytic complex of the mitochondrial inner membrane that degrades misfolded proteins and regulates ribosome assembly. In humans, it is encoded by the AFG3L2 gene. This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. And this gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders as well as spastic ataxia-neuropathy syndrome.
    UniProt
    Q9Y4W6
    途径
    Skeletal Muscle Fiber Development
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