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FANCG 抗体 (pSer383) (AbBy Fluor® 750)

This AbBy Fluor® 750-conjugated 兔 多克隆 anti-FANCG antibody specifically detects FANCG in WB, IF (cc) 和 IF (p). The antibody is reactive with 人 samples.
产品编号 ABIN5002458
发货至: 中国
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Quick Overview for FANCG 抗体 (pSer383) (AbBy Fluor® 750) (ABIN5002458)

抗原

See all FANCG 抗体
FANCG (Fanconi Anemia Complementation Group G (FANCG))

适用

  • 66
  • 5
  • 2

宿主

  • 61
  • 4
  • 1

克隆类型

  • 64
  • 2
多克隆

标记

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  • 1
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This FANCG antibody is conjugated to AbBy Fluor® 750

应用范围

  • 57
  • 25
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  • 14
  • 9
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  • 4
  • 3
  • 2
  • 1
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 22
    • 15
    • 9
    • 8
    • 5
    • 2
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    • 1
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    pSer383

    预测反应

    Human,Mouse,Rat

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic phosphopeptide derived from human FANCG around the phosphorylation site of Ser383

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    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

    FANCG (Fanconi Anemia Complementation Group G (FANCG))

    别名

    FANCG

    背景

    Synonyms: FANCG phospho S383, p-FANCG phospho S383, DNA repair protein XRCC9, DNA-repair protein XRCC9, FAG, Fanconi anaemia complementation group G, Protein FACG, X ray repair, complementing defective, in Chinese hamster cells 9, XRCC9.

    Background: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

    基因ID

    2189

    途径

    DNA Damage Repair
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