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FANCM 抗体 (AA 831-930) (HRP)

This anti-FANCM antibody (ABIN1711008) is a Rabbit Polyclonal antibody detecting FANCM in ELISA, IHC (fro), IHC (p). Suitable for Human.
产品编号 ABIN1711008
发货至: 中国

Quick Overview for FANCM 抗体 (AA 831-930) (HRP) (ABIN1711008)

抗原

See all FANCM 抗体
FANCM (Fanconi Anemia Complementation Group M (FANCM))

适用

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宿主

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克隆类型

  • 32
多克隆

标记

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This FANCM antibody is conjugated to HRP

应用范围

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ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 14
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    AA 831-930

    预测反应

    Human

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human FANCM

    亚型

    IgG
  • 应用备注

    IHC-P 1:200-400
    IHC-F 1:100-500

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    FANCM (Fanconi Anemia Complementation Group M (FANCM))

    别名

    FANCM

    背景

    Synonyms: FAAP250, Fanconi anemia group M protein, Protein Hef ortholog,

    Background: Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. The thirteen FA proteins that have been characterized are important for regulating chromosomal stability and genome surveillance. Eight of these proteins, namely FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL and FANCM, comprise the FA core complex, which catalyzes a key reaction in DNA repair: the monoubiquitination of FANCD2. FANCM (Fanconi anemia, complementation group M) is a member of the DEAD-box helicase family of proteins and contains a DEAH helicase domain and a nuclease domain. Localizing to chromatin fractions, FANCM is phosphorylated in a cell cycle-dependent manner and is believed to function as an anchor, recruiting the FA core complex to chromatin. Mutations in the gene encoding FANCM can lead to Fanconi anemia.

    基因ID

    57697

    途径

    DNA Damage Repair
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