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FANCA 抗体

FANCA 适用: 人 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7263671
发货至: 中国
  • 抗原 See all FANCA 抗体
    FANCA (Fanconi Anemia Group A Protein (FANCA))
    适用
    • 58
    • 18
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    • 2
    • 1
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    宿主
    • 70
    • 3
    克隆类型
    • 71
    • 2
    多克隆
    标记
    • 31
    • 6
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    • 3
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    • 3
    • 3
    • 2
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    This FANCA antibody is un-conjugated
    应用范围
    • 36
    • 29
    • 13
    • 13
    • 9
    • 9
    • 8
    • 4
    • 3
    • 3
    • 1
    • 1
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    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human FANCA (NP_000126.2).
    亚型
    IgG
    Top Product
    Discover our top product FANCA Primary Antibody
  • 应用备注
    IHC 1:50-1:200
    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
    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.
    基因ID
    2175
    UniProt
    O15360
    途径
    DNA Damage Repair
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