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FAM107B 抗体

FAM107B 适用: 人, 小鼠, 大鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7247411
发货至: 中国
  • 抗原 See all FAM107B 抗体
    FAM107B (Family with Sequence Similarity 107, Member B (FAM107B))
    适用
    • 13
    • 10
    • 9
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 13
    克隆类型
    • 13
    多克隆
    标记
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM107B antibody is un-conjugated
    应用范围
    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of human FAM107B
    亚型
    IgG
  • 应用备注
    IHC 1:150-1:300, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.32 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    FAM107B (Family with Sequence Similarity 107, Member B (FAM107B))
    别名
    FAM107B (FAM107B 产品)
    别名
    C10orf45 antibody, 3110001A13Rik antibody, AA589595 antibody, AA959793 antibody, AI132312 antibody, family with sequence similarity 107 member B antibody, family with sequence similarity 107, member B antibody, FAM107B antibody, Fam107b 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.
    UniProt
    Q9H098
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