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FANCA 抗体

FANCA 适用: 人 WB 宿主: 兔 Monoclonal unconjugated
产品编号 ABIN7267124
发货至: 中国
  • 抗原 See all FANCA 抗体
    FANCA (Fanconi Anemia Group A Protein (FANCA))
    适用
    • 60
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    宿主
    • 72
    • 3
    克隆类型
    • 74
    • 1
    单克隆
    标记
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    This FANCA antibody is un-conjugated
    应用范围
    • 37
    • 29
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    • 10
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    • 3
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    Western Blotting (WB)
    原理
    FANCA Rabbit mAb
    交叉反应
    产品特性
    Monoclonal Antibodies
    纯化方法
    Affinity purification
    免疫原
    A synthesized peptide derived from human FANCA
    亚型
    IgG
    Top Product
    Discover our top product FANCA Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide,0.05 % BSA,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
    FANCA (Fanconi Anemia Group A Protein (FANCA))
    别名
    FANCA (FANCA 产品)
    别名
    FA antibody, FA-H antibody, FA1 antibody, FAA antibody, FACA antibody, FAH antibody, FANCH antibody, AW208693 antibody, Fanconi anemia complementation group A antibody, Fanconi anemia, complementation group A antibody, FANCA antibody, Fanca 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 A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq, Jul 2008],FA, FA-H, FA1, FAA, FACA, FAH, FANCH,DNA Damage & Repair,Epigenetics & Nuclear Signaling,FANCA
    分子量
    163Da
    基因ID
    2175
    UniProt
    O15360
    途径
    DNA Damage Repair
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