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FANCI 抗体

FANCI 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6569525
发货至: 中国
  • 抗原 See all FANCI 抗体
    FANCI (Fanconi Anemia Complementation Group I (FANCI))
    适用
    • 14
    • 1
    • 1
    • 1
    • 1
    宿主
    • 13
    • 1
    克隆类型
    • 14
    多克隆
    标记
    • 11
    • 1
    • 1
    • 1
    This FANCI antibody is un-conjugated
    应用范围
    • 9
    • 5
    • 3
    • 2
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human FANCI
    亚型
    IgG
    Top Product
    Discover our top product FANCI Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: 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
    FANCI (Fanconi Anemia Complementation Group I (FANCI))
    别名
    FANCI (FANCI 产品)
    别名
    KIAA1794 antibody, Fanconi anemia complementation group I antibody, Fanconi anemia, complementation group I antibody, FANCI antibody, Fanci antibody
    背景

    Synonyms: FANCI,FANCI gene,FANCI,Fanconi anemia group I protein,Fanconi anemia, complementation group I,FLJ10719,FLJ14658,KIAA1794,Protein FACI,Protein FANCI

    Background: 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 I. Alternative splicing results in two transcript variants encoding different isoforms.

    分子量

    Observed_MW: 170kDa

    Calculated_MW: 27kDa/142kDa/149kDa

    基因ID
    55215
    UniProt
    Q9NVI1
    途径
    DNA Damage Repair
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