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TRIM74 抗体

TRIM74 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7244129
发货至: 中国
  • 抗原 See all TRIM74 products
    TRIM74 (Tripartite Motif Containing 74 (TRIM74))
    适用
    宿主
    • 25
    • 2
    克隆类型
    • 27
    多克隆
    标记
    • 7
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TRIM74 antibody is un-conjugated
    应用范围
    • 16
    • 16
    • 1
    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Full length fusion protein
    亚型
    IgG
  • 应用备注
    IHC 1:30-150, ELISA 1:2000-10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.1 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
    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
    TRIM74 (Tripartite Motif Containing 74 (TRIM74))
    别名
    TRIM74 (TRIM74 产品)
    别名
    TRIM50C antibody, tripartite motif containing 74 antibody, TRIM74 antibody
    背景
    TRIM 74 (Tripartite motif-containing protein 74) is a possible protein coding regions found at gene location 7q11.23. Tripartite motif (TRIM) proteins play important roles in a variety of cellular functions including cell proliferation, differentiation, development, oncogenesis, and apoptosis. TRIM gene expression analysis in primary human immune cells seem to suggest the involvement of TRIM proteins in also regulating host antiviral activities. The gene encoding TRIM 74 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
    UniProt
    Q86UV6
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