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DDI2 抗体

DDI2 适用: 人, 小鼠 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7246202
发货至: 中国
  • 抗原 See all DDI2 抗体
    DDI2 (DNA-Damage Inducible 1 Homolog 2 (DDI2))
    适用
    人, 小鼠
    宿主
    • 28
    克隆类型
    • 28
    多克隆
    标记
    • 7
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DDI2 antibody is un-conjugated
    应用范围
    • 17
    • 16
    • 2
    • 1
    ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of human DDI2
    亚型
    IgG
    Top Product
    Discover our top product DDI2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:50-1:300, 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
    DDI2 (DNA-Damage Inducible 1 Homolog 2 (DDI2))
    别名
    DDI2 (DDI2 产品)
    别名
    RP4-680D5.5 antibody, 1110056G13Rik antibody, 1700027M01Rik antibody, 9130022E05Rik antibody, AI604911 antibody, AU040698 antibody, zgc:63515 antibody, DNA damage inducible 1 homolog 2 antibody, DNA-damage inducible protein 2 antibody, DNA damage inducible 1 homolog 2 L homeolog antibody, DDI2 antibody, Ddi2 antibody, ddi2 antibody, ddi2.L antibody
    背景
    DDI1 and DDI2 are ubiquitin receptor homologs of the Saccharomyces cerevisiae ddi1 protein, which is involved in regulation of the cell cycle and the late secretory pathway. DDI2 is a 399 amino acid protein that contains one ubiquitin-like domain and exists as three isoforms as a result of alternative splicing. The gene encoding DDI2 maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8 % of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.
    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 45 kDa

    UniProt
    Q5TDH0
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