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AFG3L2 抗体 (Middle Region)

This 兔 多克隆 anti-AFG3L2 antibody specifically detects AFG3L2 in WB. The antibody is reactive with 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 斑马鱼, 山羊 和 Saccharomyces cerevisiae samples.
产品编号 ABIN2782736
发货至: 中国
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Quick Overview for AFG3L2 抗体 (Middle Region) (ABIN2782736)

抗原

See all AFG3L2 抗体
AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

适用

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人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 斑马鱼, 山羊, Saccharomyces cerevisiae

宿主

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克隆类型

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多克隆

标记

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This AFG3L2 antibody is un-conjugated

应用范围

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Western Blotting (WB)
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    Middle Region

    序列

    VNFLKNPKQY QDLGAKIPKG AILTGPPGTG KTLLAKATAG EANVPFITVS

    预测反应

    Cow: 100%, Dog: 100%, Goat: 79%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Yeast: 85%, Zebrafish: 100%

    产品特性

    This is a rabbit polyclonal antibody against AFG3L2. It was validated on Western Blot using a cell lysate as a positive control.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the middle region of human AFG3L2
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 797 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

    别名

    AFG3L2

    背景

    AFG3L2 is a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. AFG3L2 gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.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. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.
    Alias Symbols: FLJ25993, SCA28
    Protein Interaction Partner: SUMO2, UBC, SUZ12, RNF2, HIPK4, FBXO6, BTK, APP, MAPK8IP2, RAC2, ICT1, BECN1, CLN3, USP50, PHC2,
    Protein Size: 797

    分子量

    88 kDa

    基因ID

    10939

    NCBI登录号

    NM_006796, NP_006787

    UniProt

    Q9Y4W6

    途径

    Skeletal Muscle Fiber Development
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