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FANCM 抗体

FANCM 适用: 人 IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5963437
发货至: 中国
  • 抗原 See all FANCM 抗体
    FANCM (Fanconi Anemia Complementation Group M (FANCM))
    适用
    • 28
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    • 1
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    宿主
    • 26
    • 2
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    克隆类型
    • 29
    多克隆
    标记
    • 15
    • 1
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    • 1
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    • 1
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    • 1
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    This FANCM antibody is un-conjugated
    应用范围
    • 13
    • 13
    • 11
    • 8
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
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    Immunofluorescence (IF)
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human FANCM (NP_065988.1).
    亚型
    IgG
    Top Product
    Discover our top product FANCM Primary Antibody
  • 应用备注
    IF 1:50-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    FANCM (Fanconi Anemia Complementation Group M (FANCM))
    别名
    FANCM (FANCM 产品)
    别名
    FAAP250 antibody, KIAA1596 antibody, AI427100 antibody, C730036B14Rik antibody, D12Ertd364e antibody, Fanconi anemia complementation group M antibody, hypothetical protein antibody, Fanconi anemia, complementation group M antibody, FANCM antibody, PGTG_17854 antibody, Fancm antibody
    背景
    The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group M. Alternative splicing results in multiple transcript variants.
    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 75kDa/229kDa/232kDa

    基因ID
    57697
    UniProt
    Q8IYD8
    途径
    DNA Damage Repair
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