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FAM107A 抗体

FAM107A 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2423423
发货至: 中国
  • 抗原 See all FAM107A 抗体
    FAM107A (Family with Sequence Similarity 107, Member A (FAM107A))
    适用
    • 24
    • 9
    • 6
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 20
    • 4
    克隆类型
    • 22
    • 2
    多克隆
    标记
    • 14
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM107A antibody is un-conjugated
    应用范围
    • 9
    • 8
    • 6
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human FAM107A
    亚型
    IgG
    Top Product
    Discover our top product FAM107A Primary Antibody
  • 应用备注
    IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.7 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    储存液
    Sodium azide
    注意事项
    Avoid freeze / thaw cycles.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    FAM107A (Family with Sequence Similarity 107, Member A (FAM107A))
    别名
    FAM107A (FAM107A 产品)
    别名
    drr1 antibody, tu3a antibody, xdrr1 antibody, DRR1 antibody, TU3A antibody, Drr1 antibody, RGD1306327 antibody, Tu3a antibody, family with sequence similarity 107 member A S homeolog antibody, family with sequence similarity 107 member A antibody, family with sequence similarity 107, member A antibody, fam107a.S antibody, FAM107A antibody, Fam107a antibody
    背景
    FAM107B is a 131 amino acid protein that is encoded by a gene that maps to human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
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